Кафедра Органічної хімії та технології органічних речовин

Викладачі кафедри

Фокін А. А.
Рассукана Ю. В.
Василькевич О. І.
Клімко Ю. Є.
Кушко А. О.
Бутова К. Д.
Писаненко Д. А.
Родіонов В. М.
Барабаш А. В.
Гайдай О. В.
Жук Т. С.
Левандовський І. А.
Черниш Л. В.
Шамота Т. В.

Фокін Андрій Артурович

Особиста сторінка викладача

професор; Завідувач Кафедри; д.х.н.

Фокін А. А.

Проф. А.А. Фокін — спеціаліст в області синтетичної органічної, фізико-органічної та комп'ютерної хімії, а також технології органічних речовин. А.А. Фокін закінчив КПІ у 1983 році, у 1985 захистив кандидатську, а у 1994 — докторську дисертації по спеціальності 02.00.03 — органічна хімія. У 1983 році нагороджений премією Академії наук УРСР серед молодих вчених за кращу науково-дослідницьку роботу. За період роботи в КПІ проходив наукові стажування у Німеччині (Університет Ерланген-Нюрнберг, 1995, стипендія DAAD, та Університет Гьотінгена, 1997, стипендія Гумбольдта), США (Університет Джорджії, 2001 та Міннесоти, 2007). За період своєї наукової діяльності А.А. Фокін опублікував понад 120 наукових статей у рецензованих періодичних виданнях, понад 150 тез на міжнародних та Всеукраїнських наукових конференціях, є автором 12 патентів та 8 монографій виданих за межами України. Під його керівництвом захищені 8 кандидатсьих дисертацій. За останні 5 років ним опубліковані більш ніж 30 статей у найбільш рейтингових наукових виданнях (Nature, Science, Journal of the American Chemical Society, Journal of Organic Chemistry, Chemistry – A European Journal, European Journal of Organic Chemistry, Chemical Communications, Molecular Physics, Journal of Physical Chemistry, Apllpied Physics Letters та ін..) та 3 монографії у міжнародних наукових видавництвах (Wiley та Elsevier). Проф. Фокін входить до першої сотні найбільш цитованих наукових працівників України (індекс Хірша = 27) в усіх областях знань. На кафедрі він викладає 4 спеціальні дисципліни.

e-mail:
Читає курси:
Експериментальні методи дослідження процесів органічного синтезу
Методи експерименту в органічному синтезі
Теорія хімічних процесів
Комп'ютерна хімія
Сучасні проблеми органічної хімії
Сфера наукових інтересів:

Хімія каркасних сполук, активація алканів, комп'ютерна хімія радикалів та іон-радикалів, органічна електрохімія, утворення та реакції вуглеводневих катіон-радикалів, сучасні проблеми ароматичності, хімія карбенів, хімія пестицидів.

Список публікацій:

 

A)  Книги

14.  Gunawan, M. A.; Poinsot,D.;Domenichini, B.; Schreiner,. P. R.; Fokin, A. A.; Hierso, J.-C. Nanodiamonds: Emergence of Functionalized Diamondoids and their Unique Applications: in Chemistry of Organo-Hybrids: Synthesis and Characterizatioin of Functional Nano-Objects. Bernadette Charleux, Christophe Copéret, Emmanuel Lacôte, eds. 2015 John Wiley & Sons, Inc. , Hoboken, New Jersey, ISBN 978-1-11-37902-8, pp. 69–113.

13.  Shubina, T. E.; Fokin, A. A. Hydrocarbon s-radical cations. in Computational Molecular Science, v.4 Structure and Mechanism, P.R. Schreiner, W.D. Allen, M. Orozco, W. Thiel, and P. Willett, eds., Wiley 2014, pp. 2083-2101, ISBN-13:978-0-470-72307-4.

12.  Fokin, A. A. Sodiuim Methylsufinylmethylide: in Encyclopedia of reagents for organic synthesis, L. A. Paquette (Ed.), Encyclopedia of Reagents for Organic Synthesis Copyright © 2013 John Wiley & Sons, Ltd DOI: 10.1002/047084289X.rs090.pub2 Article Online Posting Date: April 22, 2013.

11.  Fokin, A. A.; Schreiner, P. R. Selective Alkane CH-Bond Substitutions: Strategies for the Preparation of Functionalized Diamondoids (Nanodiamonds), In: Strategies and Tactics in Organic Synthesis, vol. 8. M. Harmata (Ed.),Elsevier Ltd., 2012, pp. 317­–350. DOI: 10.1016/B978-0-12-386540-3.00014-9

10.    Fokin, A. A.; Schreiner, P. R. Synthesis of Theoretically Interesting and Strained Molecules. Weinheim, Wiley-VCH Verlag DmbH & KGaA, 2011, in press  (submitted, January, 2009) Elegant Total Synthesis Targets in Organic and Bioorganic Chemistry

9.      Fokin, A. A.; Schreiner, P. R. Computations on strained hydrocarbons.  In: Strained Hydrocarbons, Weinheim, Wiley-VCH Verlag DmbH & KGaA, 2009, pp. 12–18.

8.      Fokin, A. A.; Yurchenko, A. G. Common mechanisms of alkane activation with electrodeficient reagents.  in: Advances in adamantane chemistry, Moscow, Khimiya, 2007, 319 pp.

7.      Strekowski, L.; Kiselyov, A. S.; Fokin, A. A.; Schreiner, P. R. Carbon tetrabromide; in Encyclopedia of reagents for organic synthesis, L. A. Paquette (Ed.), John Wiley & Sons, Ltd. 2005, DOI: 10.1002/047084289X.rc016.pub2

6.      Schreiner, P. R.; Fokin, A. A. Carbon tetraiodide; in Encyclopedia of reagents for organic synthesis, L. A. Paquette (Ed.), John Wiley & Sons, Ltd. 2005, DOI: 10.1002/047084289X.rn00604

5.      Fokin, A. A.; Schreiner, P. R. Preparative SET C–H transformations of alkanes. in: Handbook of C–H transformations, Dyker, G.; Ed: Wiley-VCH, Vol. 2,  2005, pp. 549–554.

4.      Schreiner, P. R.; Fokin, A. A. Radical halogenations of alkanes; in: Handbook of C–H transformations, Dyker, G.; Ed: Wiley-VCH, Vol. 2,  2005, pp. 542–548.

3.      Schreiner, P. R.; Fokin, A. A.; Schleyer, P. v. R.; Schaefer III, H. F. Model studies on the electrophilic substitution of methane with various electrophiles (E=NO2+, F+, Cl+, Cl3+, HBr2+, HCO+, OH+, HO–OH+, and Li+); in: Fundamental world of quantum chemistry, Kluwer Academic Publishers, 2003, vol. II, pp. 349–375.

2.      Krasutsky, P. A.; Fokin, A. A.; Butova, E. D.; Yurchenko, A. G. Cyclic terpenes in the strain forward stereoselective pyrethroides synthesis; in: Pyrethroids, chemical and technological aspects, Moscow, Khimiya, 1992, 356 pp.

 

1.      Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Krotov, V. V.; Yurchenko, A. G.  Stereoselective pyrethroides synthesis; in:  Advances in organic chemistry, Nauka, Moscow 1989, pp. 3–25.

 

B) Статті в журналах

159. Becker, J.; Zhyhadlo, Y. Y.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Ferster, M.; Holthausen, M. C.; Specht, P.; Schindler, S.  Aerobic aliphatic hydroxylation reactions by copper complexes: A simple clip‐and‐cleave concept. Chem. Eur. J. 2018, 24, https://doi.org/10.1002/chem.201802607

158. Gebbie, M. A.; Ishiwata, H.;  McQuade P.J.; Petrak, V.: Taylor, A.; Freiwald, C.; Dahl, J. E.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Nesladek, M.; Melosh, N. A. Experimental measurement of the diamond nucleation landscape reveals classical and nonclassical features. PNAS, 2018, 115, 33, 8284–8289.

157. Moncea, O.; Poinsot, D.; Fokin, A. A.; Schreiner, P. R.; Hierso, J. C. Palladium-catalyzed C2-H arylation of unprotected (N-H)-indoles “On water” using primary diamantyl phosphine oxides as a class of primary phosphine oxide ligands. ChemCatChem, 2018, 10, 2915 – 2922.

156. Hoc, N. T.  Fokin, A. A; Rodionov, V. N. Synthesis of 10-methoxydiamantan-3-one. MOLBANK. 2018, 2, UNSP M990. DOI: 10.3390/M990

155. Hoc, N. T.  Fokin, A. A; Rodionov, V. N. Towards 3-(2-adamantylidene)diamantane derivatives through the McMurry cross coupling reaction. Org. Commun. 2018, 11, 2x, 75-79.

154. Yan, H.; Narasimha, K. T.; Denlinger, J.; Li, F. H.; Mo, S.-K.; Nathan Hohman, J.;  Dahl, J. E. P.; , Carlson, R. M. K.; Tkachenko, B. A.;Fokin, A. A.; Schreiner, P. R.; Hussain, Z.; Shen, Z.-X.; ,Melosh, N. A.Monochromatic photocathodes from graphene-stabilized diamondoids. Nano Lett., 2018, 18, 1099–1103.

153. Yan, H.; Yang, F.; Pan, D.; Lin, Y.; Hohman, J. N.; Solis-Ibarra, D.; Li, F. H.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Galli, G.; Mao, W. L.; Shen Z.-X.; Melosh, N. M. Sterically controlled mechanochemistry under hydrostatic pressure. Nature 2018, 554, 505–510.

152. Gunawan, M. A.; Moncea, O.; Poinsot, D.; Keskes, M.; Domenichini, B.; Heintz, O.; Chassagnon, R.; Herbst, F.; Carlson, R. M. K.; Dahl, J. E. P.; Fokin, A. A.; Schreiner, P. R.; Hierso,  J.-C. Nanodiamond-Palladium Core–Shell Organohybrid Synthesis: A Mild Vapor-Phase Procedure Enabling Nanolayering Metal onto Functionalized sp3-Carbon. Adv. Funct. Mater. 2018, 1705786 (15 p).

151. Gunchenko, P. A.; Li,J.; Liu, B.; Chen, H.; Pashenko, A. P.;Bakhonsky, V. V.; Zhuk. T. S.; Fokin, A. A. Aerobic oxidations with N-hydroxyphthalimide in trifluoroacetic acid. Molec. Cat. 2018, 446, 72-79.

150. Zhyhadlo, Y. Y.; Gaidai, A. V.; Sharapa, D. I.; Mitlenko, A. G.; Shishkin, O. V.; Shishkina, S. V.; Levandovskiy, I. A.; Fokin, A. A. Functionalised Cookson's diketones in chlorosulfonic acid: Towards polysubstituted D3-trishomocubanes. J. Chem. Res. 2017, 41, 12, 677-733.

149. Tyborski, C.; Gillen, R.; Fokin, A. A.; Koso, T. V.; Fokina, N. A.; Hausmann, H.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. Electronic and Vibrational Properties of Diamondoid Oligomers. J. Phys. Chem. 2017, 121, 48, 27082–27088

148. Fokin, A. A.: Zhuk, T. S.; Blomeyer, S.; Peŕez, C.;  Chernish, L.V.; Pashenko, A. E.; Antony, J.; Vishnevskiy, Y. V.;  Berger, R. J. F.; Grimme, S.; Logemann, C.; Schnell, M.; Mitzel N. W.; Schreiner P. R. Intramolecular London dispersion interaction effects on gas-phase and solid-state structures of diamondoid dimers. J. Amer. Chem. Soc. 2017, 139, 16696-16707.

147. Tyborski, C.; Meinke, R.; Gillen, R.; Bischoff, T.; Knecht, A.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N. Schreiner, P. R.; Moller, T.; Rander, T.; Thomsen, C.; Maultzsch, J. From isolated diamondoids to a van-der-Waals crystal: A theoretical and experimental analysis of a trishomocubane and a diamantane dimer in the gas and solid phase. J. Chem. Phys. 2017, 147, 4, 044303 (6 p.)

146. Fokin, A. A.; Pashenko, A. E.; Bakhonsky, V. V.; Zhuk. T. S.; Chernish. L. V.; Gunchenko, P. A.; Kushko, A. O.; Becker, J.; Wende, R. C.; Schreiner. P. R. Chiral building blocks based on 1,2-disubstituted diamantanes. Synthesis, 2017. 49, 20032008.

145.     Yan, H.; Hohman, J. N.; Li, F. H.; Jia, C.; Solis-Ibarra, D.; Wu, B.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Vailionis, A.; Kim, T. R.; Devereaux, T. P.; Shen, Z.-X.; Melosh. N. A. Hybrid metal–organic chalcogenide nanowires with electrically conductive inorganic core through diamondoid-directed assembly. Nat. Mater. 2017, 16, 349–355.

144.  Hoc, N. T.;Kushko, A. O.;Fokin, A. A.;Rodionov, V. N. Functional derivatives of diamantanone. Russ. J. Org. Chem. 2016, 52, 8, 1209–1211.

143. Moncea O.; Gunawan, M. A.; Poinsot,D.; Cattey. H.;Becker,J.;Yurchenko,R. I.; Butova,E. D.; Hausmann,H.; Šekutor,M.; Fokin, A. A.; Hierso,J.-C.; Schreiner, P. R. Defying stereotypes with nanodiamonds: Stable primary diamondoid phosphines,  J. Org. Chem. 2016, 81, 8759−8769.

142.     Tverdiy, D. O. Chekanov, M. O.; Savitskiy, P. V.; Syniugin, A. R.; Yarmoliuk, S. M. Fokin, A. A. Efficient preparation of imidazo[1,5-a]pyridine-1-carboxylic acids. Synthesis 2016, 48, A–I.

141.     Ponomarenko, M. V.; Grabowsky,S.; Pal,R.; Röschenthaler, G.-V., Fokin, A. A. SF5-Enolates in Ti(IV)-mediated aldol reactions. J. Org. Chem. 2016, 81, 6783−6791.

140. Karthik, T. N.; Ge,C.; Fabbri,J. D.; Clay,W.; Tkachenko, B. A.; Fokin, A.A.; Schreiner, P. R.; Dahl, J. E.; Carlson, R. M. K.; Shen, Z. X.; Melosh, N. A. Ultra-low effective work function surfaces using diamondoid monolayers. Nature Nanotech. 2016, 11, 267–273.

139. Zhang, J. L.; Ishiwata, H.; Babinec, T. M.; Radulaski, M.; Müller, K.; Lagoudakis, K. G.; Dory, C.; Dahl, J.; Edgington, R.; Soulière, V.; Ferro, G.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N.; Vuckovic, J. Hybrid group IV nanophotonic structures incorporating diamond silicon-vacancy color centers. Nano Lett. 2016, 16, 212−217.

138. Syniugin, A. R.; Chekanov, M. O.; Savitskiy, P. V.; Pashenko, A. E.; Zhuk, T. S.; Yarmoluk, S. M.; Fokin, A A. New method for the synthesis of pyrrolo[2,3-b]dihydroquinolines. Tetrahedron Lett.  2016, 57, 213–215.

137. Valentin, L.; Henss, A.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Becker, S.; Würtele, C.; Schindler, S. Transition metal complexes with cage-opened diamondoid tetracyclo[7.3.1.14,12.02,7]tetradeca-6.11-diene. J. Coor. Chem. 2015, 68, 3295–3301.

136. Lourie, L. F.; Serguchev, Yu. A.; Bentya, A. V.; Ponomarenko, M. V.; Rusanov, E. B.; Vovk, M. V.; Fokin, A. A.; Ignat’ev, N. V. Metal free electrophilic fluoro-cyclization of unsaturated N-hydroxy- and N-acetoxyamides with N–F reagents. J. Fluor. Chem. 2015, 179, 42–47.

135. Bremer, M.; Untenecker, H.; Gunchenko, P. A.; Fokin, A. A.; Schreiner P. R.  Inverted carbon geometries: Challenges to experiment and theory. J. Org. Chem. 2015, 80, 6520−6524.

134. Zhuk, T. S.; Koso, T.; Pashenko, A. E.; Hoc, N. T.; Rodionov, V. N.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Toward an understanding of diamond sp2-defects with unsaturated diamondoid oligomer model. J. Am. Chem. Soc. 2015, 137, 6577−6586.

133. Gunawan, M. A.; Poinsot, D.; Domenichini, B.; Dirand, C.; Chevalier, S.; Fokin, A. A.; Schreiner, P. R.; Hierso, J.-P. The functionalization of nanodiamonds (diamondoids) as a key parameter of their easily controlled self-assembly in micro- and nanocrystals from the vapor phase. Nanoscale, 2015, 7, 1956–1962.

132. Barabash, A. V.; Didukh, N. A.; Kibal’nyi, N. A.; Butova, E. D.; Schreiner, P. R.;Fokin, A. A. Unusual aerobic oxidation of sterically hindered 1-diamanty methyl ketone. Russ. J. Org. Chem. 2014, 50, 1690–1691.

131.  Gunchenko, P. A.; Novikovskii, A. A.; Byk, M. V.; Fokin, A. A.  Structure and transformations of diamantane radical cation: Theory and experiment. Russ. J. Org. Chem. 2014, 50, 1749–1754.

130. Mishura, A. M.; Sklyarova, A. S.; Shamota, T. V.: Rodionov, V. N.; Fokin, A. A.  Preparative synthesis of pentacyclo[6.3.0.02,6.03,10.05,9]undecan-4-one (D3-Trishomocubanone). Russ. J. Org. Chem. 2014, 50, 1542–1544.

129. Barabash, A. V.; Butova, E. D.; Kanyuk, I. M.; Schreiner, P. R.; Fokin, A. A. Beyond the Corey reaction II: Dimethylenation of sterically congested ketones J. Org. Chem. 2014, 79, 10669−10673. ACS Editor’s Choice, 01.10.2014.

128. Randel, J. C.; Niestemski, F. C.; Botello-Mendez, A. R.; Mar, W.; Ndabashimiye, G.; Melinte, S.; Dahl, J. E. P.; Carlson R. M. K.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Charlier, J.-C.; Manoharan, H. C. Unconventional molecule-resolved current rectification in diamondoid fullerene hybrids. Nature Comm. 2014, 5, 4877 (6 p).

127. Tchernobaev, I. I.; Serguchev, Yu. A.; Fokin, A. A. Mechanism and selectivities of the chlorination of toluene in the presence of catalytical composition antimony pentachloride – benzodithio crown ether. Ukr. Krim. Zhurn. 2014, 50, 45–49.

126. Ponomarenko, M. V.; Serguchev, Yu. A.; Hirschberg, M. E.; Röschenthaler, G.-V.; Fokin, A. A. Elemental F2 with transannular dienes: Regioselectivities and mechanisms. Chem. Eur. J. 2014, 20, 10383–10391.

125. Fokin, A.A.; Yurchenko, R. I.; Tkachenko,B.A.; Fokina,N. A.; Gunawan,M. A.; Poinsot,D.; Dahl, J. E. P.; Carlson,R. M. K.; Serafin,M.; Cattey,H.; Hierso,J.-C.; Schreiner, P. R. Selective preparation of diamondoid phosphonates. J. Org. Chem. 2014, 79, 5369–5373.

124. Fokin, A. A.; Zhuk, T. S.; Pashenko, A. E.; Osipov, V. V.; Gunchenko,P. A.; Serafin, M.; Schreiner, P. R. Functionalization of homodiamantane: Oxygen insertion reactions without rearrangement with dimethyldioxirane. J. Org. Chem. 2014, 79, 1861–1866.

123. Meinke, R.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. UV resonance Raman analysis of trishomocubane and diamondoid dimers. J. Chem. Phys. 2014, 140, 034309 (5p).

122. Kahl, P.; Tkachenko, B. A.; Novikovsky, A. A.; Backer, J.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.  Efficient peparation of aically substituted damondoid drivatives, Synthesis 2014, 46, 787–798.

121. Gunawan, M. A.; Hierso, J.-C.; Poinsot, D.; Fokin, A. A.; Fokina, N. A.; Tkachenko, B. A.;Schreiner, P. R. Diamondoids: Functionalization and subsequent applications of perfectly defined molecular cage hydrocarbons. New J. Chem. 2014, 38, 28–41.

120.     Chekanov, M. O.; Ostrynska, O. V.; Tarnavskyi, S. S.; Synyugin, A. R.; Briukhovetska, N. V.; Bdzhola, V. G.; Pashenko, A. E.; Fokin A. A.; Yarmoluk, S. M. Design, synthesis and biological evaluation of 2-aminopyrimidinones and their 6-aza-analogs as a new class of СК2 inhibitors. J. Enz. Inhib. Med. Chem. 2014, 29, 5, 639­–646.

119.     Ponomarenko, M. V.; Lummer, K.; Fokin, A. A.; Serguchev, Yu. A.; Bassil, B. S.; Röschenthaler, G.-V.  Preparations of SF5- and CF3-substituted arenes utilizing the 7-oxabicyclo­[2.2.1]hept-2-ene synthones. Org. Biomol. Chem. 2013, 11, 8103­–8112.

118.     Kacharov, A. D.; Yemets, S. V.; Nemykin,V. N.; Kacharova, L. M.; Fokin,A. A.; Krasutsky, P. A. Stereoselectivity of A-ring contraction for 3-oxotriterpenoids.  RCS Advances 2013, 3, 19057–19063.

117.     Mishura, A. M.; Sklyarova, A. S.; Sharapa, D. I.; Levandovsky, I. A.; Serafin, M.; Fokin, A. A.; Rodionov, V. N. Stereoselective Preparation of mono- and bis-derivatives of pentacyclo[6.3.0.02,6.03,10.05,9]undecane (D3-trishomocubane). Open. Chem.  2013, 11, 2144–2150.

116. Li, F. H.; Fabbri, J. D.; Yurchenko, R. I.; Mileshkin, A. N.; Hohman, J. N.; Yan, H.; Yuan, H.; Tran, I. C.; Willey, T. M.; Bagge-Hansen, M.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N. A. Covalent attachment of diamondoid phosphonic acid dichlorides to tungsten oxide surfaces. Langmuir 2013, 29, 9790–9797.

115. Zimmermann, T.; Richter, R.; Knecht, A.; Fokin, A. A.; Koso, T. V.; Chernish, L. V.; Gunchenko, P. A.; Schreiner, P. R.; Moller, T.; Rander, T. Exploring covalently bound diamondoid aggregates with valence photoelectron spectroscopy. J. Chem. Phys. 2013, 139, 084310 (6 p).

114. Fokin, A. A.; Butova, E. D.; Barabash, A. V; Huu, N. N.; Tkachenko. B. A.; Fokina, N. A.; Schreiner, P. R. Preparative synthesis of vinyl diamondoids. Synth. Comm. 2013, 43, 1772–1777.

113. Sklyarova, A. S.; Rodionov, V. N.; Parsons, C. G.; Quack, G.; Schreiner, P. R.; Fokin, A. A. Preparation and testing of homocubyl amines as therapeutic NMDA receptor antagonists. Med. Chem. Res. 2013, 22, 360–366.

112.     Clay, W. A.; Maldonado, J. R.;  Pianetta, P.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Melosh, N.; Shen, Z.-X. Photocathode device using diamondoid and cesium bromide films Appl. Phys. Lett. 2012, 101, 241605 (5p).

111. Ishiwata, H.; Acremann, Y.; Scholl, A.; Rotenberg, E.; Hellwig, O.; Dobisz, E.; Doran, A.; Tkachenko, B.A.; Fokin, A.A.; Schreiner, P.R.; Dahl, J.E.P.; Carlson, R.M.K.; Melosh, N.; Shen, Z.-X.; Oldag, H. Diamondoid coating enables disruptive approach for chemical and magnetic imaging with 10 nm spatial resolution. Appl. Phys. Lett. 2012, 101, 163101 (5 p).

110. Fokin, A. A.;  Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Hausmann, H.; Serafin, M.; Dahl J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Stable alkanes containing very long carbon–carbon bonds. J. Am. Chem. Soc. 2012, 134, 13641–13650.

109. Gunchenko, P. A.; Fokin, A. A. Mechanisms of activation of C–H bonds in framework compounds: Theory and experiment. Theoret. Experim. Khim. 2012, 47, 6, 343–360.

108. Gaidai, A. V.; Volochnyuk, D. M.; Shishkin, O. V.; Fokin, A. A.; Levandovskiy, I. A.; Shubina, T. E. D3-Trishomocubane-4-carboxylic acid as a new chiral building block: Synthesis and absolute configuration. T. E. Synthesis 2012, 44, 810–816.ю

107. Fokina, N. A.; Tkachenko, B. A.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner P. R.  Synthesis of diamondoid carboxylic acid. Synthesis 2012, 44, 259–264.1

106. Fokin, A. A.; Gerbig, D.; Schreiner, P. R. σ/σ- and π/π-Interactions are equally important: multilayered graphanes. J. Am. Chem. Soc. 2011, 133, 20036–20039.

105. Rodionov, V. N.; Sklyarova, A. S.; Shamota, T. V.; Schreiner, P. R.; Fokin, A. A. Selective reductive dimerization of homocubane series oximes. Russ. J. Org. Chem. 2011, 47, 11, 1695−1702.

104.     Schreiner, P. R.; Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Hausmann, H.; Serafin, M.; Schlecht, S.; Dahl J. E. P.; Carlson, R. M. K.; Fokin, A. A. Overcoming  lability of extremely long alkane carbon–carbon bonds through dispersion forces. Nature 2011, 477, 308–311. This paper was featured in Chemical & Engineering News, 89(38), September 19, 2011 [Science & Technology, Concentrates]

103. Novikovskii, A. A.; Gunchenko P. A.; Prikhodchenko P. G.; Serguchev, Yu. A.; Schreiner P. R.; Fokin A.A. Comparative theoretical and experimental analysis of hydrocarbon σ-radical cations. Russ. J. Org. Chem. 2011, 47, 1293–1299.

102.     Shubina, T. E.; Fokin, A. A. Hydrocarbon s-radical cations. WIREs Comput. Mol. Sci. 2011, 1 661– 679.

101. Serguchev, Yu. A.; Ponomarenko, M. V.; Lourie, L. F.; Fokin, A. A. Transannular additions of selectfluor and xenon difluoride: regioselectivity and mechanism. J. Phys. Org. Chem. 2011, 24, 407–413.

100.     Butova, E. D.; Barabash, A. V.; Petrova, A. A.; Kleiner, C. M.; Schreiner, P. R.; Fokin. A. A. Stereospecific consecutive epoxide ring expansion with dimethylsulfoxonium methylide, J. Org. Chem. 2010, 75, 18, 6229–6235.

99.    Demchenko, P. Yu.; Gladyshevskii, R. E.; Volkov, S. V.; Kharkova, L. B.; Yanko, O. G.; Fokina, Z. A.; Fokin, A. A. The first nonaselenium ring. Chem. Commun. 2010, 46, 4520–4522.

98.  Lysenko, A. B.; Senchyk, G. A.; Lincke, J.; Lässig, D.; Fokin, A. A.; Butova, E. D.; Schreiner, P. R.; Krautscheid, H.; Domasevitch, K. V. Metal oxide-organic frameworks (MOOFs), a new series of coordination hybrids constructed from molybdenum(VI) oxide and bitopic 1,2,4-triazole linkers. Dalton Trans. 2010, 39, 4223–4231.

97.  Zhuk, T. S.; Bratko, E. Y.; Pashenko, A. E.; Gunchenko, P. A.; Yurchenko, A. G.; Schreiner, P. R.; Fokin, A. A. The “green” synthesis of neuroprotecting drug Memantine. J. Org. Pharm. Chem. 2010, 8, 62–66.

96.  Roth, S.; Leuenberger, D.; Osterwalder, J.; Dahl, J. E.; Carlson, R. M. K.; Tkachenko, B. A. Fokin, A. A.; Schreiner, P. R., Hengsberger, M. Negative-electron-affinity diamondoid monolayers as high-brilliance source for ultrashort electron pulses. Chem. Phys. Lett.  2010, 495, 102–108.

95.  Landt, L.; Bostedt, C.; Wolter, D.; Möller, T.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Kulesza, A.; Bonacic-Koutecky, V. Experimental and theoretical studies of the absorption properties of thiolated diamondoids. J. Chem. Phys. 2010, 132, 144305 (6p).

94.  Landt, L.; Staiger, M.; Wolter, D.; Klünder, K.; Zimmermann, P.; Willey, T. M.; van Buuren, T.; Brehmer, D.; Schreiner, P. R.; Tkachenko, B. A.; Fokin, A. A.; Möller, T.; Bostedt, C. The influence of a single thiol group on the electronic and optical properties of the smallest diamondoid adamantane. J. Chem. Phys. 2010, 132, 0247101(7p).

93.  Levandovskiy, I. A.; Shubina, T. E.; Fokin, A. A. Computational and QSAR study of the alkylnaphthyl ketones adsorption on silver-ion stationary phase.  J. Molec. Mod. 2010, 16, 513–522.

92.  Schreiner, P. R.; Fokin, A. A.; Reisenauer, H. P.;  Tkachenko, B. A.; Vass, E.; Olmstead, M. M.; Bläser, D.; Boese, R.; Dahl, J. E. P.; Carlson, R. M. K. [123]Tetramantane: Parent of a new family of σ-helicenes. J. Am. Chem. Soc. 2009, 131, 11292–11293.

91.  Fokin, A. A.; Gunchenko, P. A.; Novikovsky, A. A.; Shubina, T. E.; Chernyaev, B. V.; Dahl J. E. P.; Carlson, R. M. K.; Yurchenko, A. G.; Schreiner P. R. Photoacetylation of diamondoids: Selectivities and mechanism. Eur. J. Org. Chem. 2009, 5153–5161. This work is featured: Cover picture of the Eur. J. Org. Chem., 2009, issue 30.

90.  Fokin, A. A.; Zhuk, T. S.; Pashenko, A. E.; Dral, P. O.; Gunchenko, P. A.; Dahl, J. E. P.;Carlson, R. M. K.;Koso, T. V.;Serafin, M.; Schreiner, P. R. Oxygen-doped nanodiamonds: Synthesis and functionalizations. Org. Lett. 2009, 11, 3068–3071.

89.  Sklyarova, A. S.; Rodionov, V. N.; Fokin, A. A. A convenient preparative synthesis of pentacyclo[5.3.0.02,5.03,9.04,8]decane (C2-bishomocubane). Russ. J. Org. Chem. 2009, 45, 11, 1644−1647.

88.  Gunchenko, P. A.; Makuhina, A. M.; Novikovsky, A. A.; Yurchenko, A. G.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Structure and transformations of homoadamantane radical cation.  Theoret. and Experim. Khim. 2009, 45, 4, 246–251.

87.  Willey, T. M.; Lee, J. R. I.; Fabbri, J. D.; Wang, D.; Nielsen, M. H.; Randel, J. C.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Dahl, J. E. P.; Carlson, R. M. K.; Terminello, L. J.; Melosh, N. A.; van Buuren, T. Determining orientational structure of diamondoid thiols attached to silver using near-edge X-ray absorption fine structure spectroscopy. J. Elec. Spectr. Rel. Phen. 2009, 172, 69–77.

86.  Schwertfeger, H.; Würtele, C.; Hausmann, H.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R. Selective preparation of diamondoid fluorides. Adv. Synth. Catal. 2009, 351, 1041–1054.

85.  Fokin, A. A.; Schreiner, P. R. Band gap tuning in nanodiamonds: First principle computational studies. Molec. Phys. 2009, 107, 8–12, 823–830.

84.  Fokin, A. A.; Tkachenko, B. A.; Fokina, N.  A.; Hausmann, H.; Serafin, M.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Reactivities of the prism-shaped diamondoids [1(2)3]tetramantane and [12312]hexamantane (cyclohexamantane). Chem. Eur. J. 2009, 15, 3851–3862.

83.  Fokin, A. A.; Merz, A.; Fokina, N. A.; Schwertfeger, H.; Liu, S. L.; Dahl, J. E. P.; Carlson, R. K. M.; Schreiner, P. R.  Synthetic routes to aminotriamantanes, topological analogues of the neuroprotector memantine. Synthesis 2009, 909–912.

82.  Clay, W. A.; Liu, Z.; Yang, W.; Fabbri, J. D.; Dahl, J. E.; Carlson, R. M. K.; Sun, Y.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Pianetta, P. A.; Melosh, N.; Shen Z.-X. Origin of the monochromatic photoemission peak in diamondoid monolayers. Nano Lett. 2009, 9, 57–61.

81.  Willey, T. M.; Fabbri, J. D.; Lee, J. R. I.; Schreiner, P. R.; Fokin, A. A.; Fokina, N. A; Dahl, J. E. P.; Carlson, R. M. K.; Vance, A. L.; Yang, W.; Terminello, L. J.; van Buuren, T.; Melosh, N. A.  Near-edge X-ray absorption fine structure spectroscopy of diamondoid thiol monolayers on gold.  J. Am. Chem. Soc. 2008, 130, 10536–10544.

80.  Chernish, L. V.; Gunchenko, P. A.; Barabash, A. B.; Goreslavets, V. S.; Yurchenko, A. G.; Fokin, A. A. Selective synthesis of 1,1-diadamantane monoderivatives.  Zhurn. Org. Pharm. Khim. 2008, 6, 48–51.

79.  Zhuk, T. S.; Gunchenko, P. A.; Korovai, Ya. Yu.; Schreiner,P. R.; Fokin A. A. Mechanisms of the C–H halogenation of adamantane in the presence of N-hydroxyphthalimide.   Theoret. and Experim. Khim.  2008, 44, 1, 46–51.

78.  Schwertfeger, H; Fokin, A. A.; Schreiner, P. R. Diamonds are a chemist’s best friend: Diamondoid chemistry beyond adamantane.  Angew. Chem. Int. Ed. 2008, 47, 1022–1036.

77.  Fokin, A. A.; Yurchenko, A. G.; Rodionov, V. N.; Gunchenko, P. A.; Yurchenko, R. I.; Reichenberg, A.; Wiesner, J.; Hintz, M.; Jomaa, H.; Schreiner, P.R. Synthesis of the antimalarial drug FR900098 utilizing the nitroso-ene reaction. Org. Lett. 2007, 9, 4379–4382. G

76.  Fokina, N. A.; Tkachenko, B. A.; Merz, A.; Serafin, M.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R. Hydroxy derivatives of diamantane, triamantane, and [121]tetramantane: Selective preparation of bis-apical derivatives. Eur. J. Org. Chem. 2007, 4738–4745.

75.  Butova, E. D.; Fokin, A. A.; Schreiner, P. R. Beyond the Corey reaction: One-Step diolefination of cyclic ketones. J. Org. Chem. 2007, 72, 5689–5696.

74.  Fokin, A. A.; Butova, E. D.; Chernish, L. V.; Fokina, N. A.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Simple preparation of diamondoid 1,3-dienes via oxetane ring opening. Org. Lett. 2007, 9, 2541–2544.0

73.  Yang, W. L.; Fabbri J. D.; Willey, T. M.; Lee, J. R. I.; Dahl, J. E.; Carlson, R. M. K.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Meevasana, W.; Mannella, N.; Tanaka, K.; Zhou, X. J.; van Buuren, T.; Kelly, M. A.; Hussain, Z.; Melosh, N. A.; Shen, Z.-X. Monochromatic electronphotoemission from diamondoid monolayers. Science 2007, 316, 1460–1462.

72.       Wodrich, M. D.; Corminboeuf, C.; Schreiner, P. R.; Fokin, A. A.; Schleyer, P. v. R. How accurate are DFT treatments of organic energies? Org. Lett. 2007, 9, 1851–1854.

71.  Schreiner, P. R.; Fokin, A. A.; Pascal, R. A., Jr.; de Meijere, A. Many density functional theory approaches fail to give reliable large hydrocarbon isomer energy differences. Org. Lett. 2006, 8, 3635–3638.

70.  Fokin, A. A.; Schreiner, P. R.; Fokina, N. A.; Tkachenko, B. A.; Hausmann, H.; Serafin, M. Dahl, J. E. P.; Liu, S.; Carlson, R. M. K.  Functionalized nanodiamonds Part 4: Reactivity of [1(2,3)4]pentamantane (Td-Pentamantane): A nanoscale model of diamond J. Org. Chem. 2006, 71, 8532–8540.

69.   Ponomarenko, M. V.; Serguchev Y. A.; Ponomarenko, B. V.; Röschenthaler, G.-V.; Fokin, A. A. Experimental and theoretical studies on the transannular cyclizations of 3,7-dimethylenebicyclo[3.3.1]nonane with polyfluoroalkyl radicals.  J. Fluor. Chem, 2006, 127, 842–849.

68.  Schreiner, P. R.; Fokina, N. A.; Tkachenko, B. A.; Hausmann, H.; Serafin, M.; Dahl, J. E. P.; Liu, S.; Carlson, R. M. K.; Fokin, A. A. Functionalized Nanodiamonds Part 2: Triamantane and [121]Tetramantane. J. Org. Chem. 2006, 71, 18, 6709–6720. This work is featured: Cover picture of the J. Org. Chem., 2006, issue 18.

67.  Tkachenko, B. A.; Fokina, N. A.; Chernish, L. V.; Dahl, J. E. P.; Liu, S.; Carlson, M. K.; Fokin, A. A.; Schreiner, P. R. Functionalized Nanodiamonds Part 3: Thiolation of tertiary/bridgehead alcohols. Org. Lett. 2006, 8, 1767–1770.

66.  Fokin, A. A.; Schreiner, P. R.; Berger, R.; Robinson, G. H.; Wei, P.; Campana, C. F. Pseudotetrahedral polyhalocubanes: Synthesis, structures, and parity violating energy differences. J. Am. Chem. Soc. 2006, 128, 5332–5333. This work is featured: Nature, 2006, 44, 4, 5.

65.  Fokin, A. A.; Tkachenko, B. A.; Gunchenko, P. A. Gusev, D. V. Schreiner, P. R. Functionalized Nanodiamonds Part I. An experimental assessment of diamantane and computational predictions for higher diamondoids. Chem. Eur. J. 2005, 11, 7091–7101.

64.  de Meijere, A.; Lee, C.-H.; Kuznetsov M. A.; Gusev, D. V.; Kozhushkov, S. I.; Fokin, A. A.; Schreiner, P. R. Preparation and reactivity of [D3d]-octahedrane: The most stable (CH)12 hydrocarbon. Chem. Eur. J. 2005, 11, 6175–6184.

63.  Rodionov, V. N.; Chernyaev, B. V.; Levandovskii, I. A.; Shubina, T. E.; Fokin, A. A..  Quantum-chemical interpretation of the reorientation of dialkyl-cis-9,10-dihydroanthracene-9,10-endofumarates on a silver-containing stationary phase.  Theoret. and Experim. Khim. 2005, 41, 1, 1–6.

62.  Rodionov, V. M.; Chernyaev, B. V.; Levandovs'kii, I. A.; Shubina, T. E.; Fokin, A. A.; Yurchenko, O. G.  Experimental and quantum-chemical study of the thermodynamics of complexation of methylbenzenes with silver(I) ion.          Naukovi Visti - Natsional'nii Tekhnichnii Universitet Ukraini "Kiivs'kii Politekhnichnii Institut"  2005, 1, 107–115.

61.  Fokin, A. A.; Tkachenko, B. A.; Gunchenko, P. A.; Schreiner, P. R. The protonation of cubane revisited. Angew. Chem. Int. Ed. 2005, 44, 146–149.

60.  Schreiner, P. R.; Fokin, A. A.; Kotke, M.; Weil, T. Noncovalent organocatalysis.  Ann. Pol. Chem. Soc. 2004, 3, part 1, 21–24.

59.  Schreiner, P. R.; Fokin, A. A. Selective alkane C–H-bond functionalizations utilizing oxidative single-electron transfer and organocatalysis. Chem. Record 2004, 3, 247–257.

58.  Kiriy, N.; Jahne, E.; Adler, H.-J.; Schneider, M.; Kiriy, A.; Gorodyska, G.; Minko, S.; Jehnichen, D.; Simon,|P.; Fokin, A. A.; Stamm, M. One-dimensional aggregation of regioregular polyalkylthiophenes. Nano Letters 2003, 3, 707–712.

57.  Gunchenko, P. A.; Vigovskaya, T. S.; Fokin, A. A.; Yurchenko, A. G. A New method for building of [3.3.3]propellan skeleton.  Ukr. Khim. Zhurn. 2003, 69, 10, 113–115.

56.  Fokin, A. A.; Schreiner, P. R. Metal-free, selective alkane functionalizations.  Adv. Chem. Cat. 2003, 345, 1035–1052.

55.  de Meijere, A.; Kozhushkov, S. I.; Fokin, A. A.; Emme, I.; Redlich, S.; Schreiner, P. R. New structurally interesting cyclopropane derivatives. A world of wonders and surprises. Pure Appl. Chem. 2003, 75, 549–562.

54.  Fokin, A. A.; Schreiner, P. R.; Kozhushkov, S. I.; Sattelmeyer, K. W.; Schaefer, H. F.; de Meijere, A. Delocalizations in s-radical cations: The Intriguing structures of ionized [n]rotanes.  Org. Lett. 2003, 5, 697–700

53. Tkachenko, B. A.; Shubina, T. E.; Gusev, D. V.; Gunchenko, P. A.; Yurchenko, A. G.; Schreiner, P. R.; Fokin, A. A. Mechanisms of C–H Activation of Alkanes by Chromium-oxo Reagents.  Theoret. and Experim. Khim. 2003, 39, 2, 90–95.

52.   Krasutsky, P. A.; Kolomitsyn, I. V.; Botov, E. M.; Carlson, R. M.; Semenova, I. G.; Fokin, A. A. Heterolytic decarboxylation involving acyltrifluoroacetyl peroxide intermediates. Tetrahedron Lett. 2002, 43, 8687–8691.

51.  Schreiner, P. R.; Fokin, A. A.; Lauenstein, O.;  Okamoto, Y.; Wakita, T.; Rinderspacher, C; Robinson, G. H.; Vohs, J. K.; Campana.; C. F. Pseudotetrahedral polyhaloadamantanes as chirality probes: Synthesis, separation, and absolute configuration.  J. Am. Chem. Soc. 2002, 124, 13348–13349.

50.  Fokin, A. A.; Tkachenko, B. A.; Shubina, T. E.; Gunchenko, P. A.; Gusev, D. V.; Vohs, J. K.; Robinson, R. H.; Yurchenko, A. G.; Schreiner, P. R. The protoadamantane radical cation.  Eur. J. Org. Chem. 2002, 3844–3849.

49.  Shubina, T. E.; Gunchenko, P. A.; Vigovskaya, T. S.; Schreiner, P. R.; Yurchenko, A. G.; Fokin, A. A.  [3.3.2]- and [3.3.3]propellanes in reactions with oxidizing electrophiles. Teoret. i Experim. Khimiya, 2002, 38, 4, 226–231.

46.  Kiriy, A. V.; Yurchenko, A. G.; Fokin, A. A. The new [2,3]-sigmatropic rearrangement of allylsulfinyl carbanions. Russ. J. Org. Chem. 2002, 38, 3, 471–472.

48.  Fokin, A. A.; Shubina, T. E.; Gunchenko, P. A.; Isaev, S. D.; Yurchenko, A. G.; Schreiner, P. R. H-Coupled electron transfer in alkane C–H activations with halogen electrophiles. J. Am. Chem. Soc. 2002, 124, 10718–10727.

47.  Fokin, A. A.; Schreiner, P. R. Selective alkane transformations via radicals and radical cations: Insights into the activation step from experiment and theory. Chem. Rev. 2002, 102, 1551–1593.

45.  Shubina, T. E.; Gunchenko. P. A.; Yurchenko, A. G.; Schreiner, P. R.; Butova, E. D.; Fokin, A. A. Structure and transformations of 1-alkyladamantane radical cations.  Teoret. i Experim. Khimiya 2002, 38, 1, 8–13.

44.  Schreiner, P. R.; Lauenstein, O.; Butova, E. D.; Gunchenko, P. V.; Kolomitsin, I. V.; Wittkopp, A.; Feder, G.; Fokin, A. A. Selective radical reactions in multiphase systems: Phase-transfer halogenations of alkanes. Chem. Eur. J. 2001, 7, 23, 4996–5003.

43.  Fokin, A. A.; Tkachenko, B. A.; Korshunov, O. I.; Gunchenko, P. A.; Schreiner, P. R. Molecule-induced alkane homolysis with dioxiranes. J. Am. Chem. Soc. 2001, 123, 11248–11252.

42.  Prall, M.; Wittkopp, A.; Fokin, A. A.; Schreiner, P. R.  Substituent effects on the Bergman Cyclization of (Z)-1,5-hexadiyne-3-enes: A systematic computational study. J. Comp. Chem. 2001, 22, 13, 1605–1614.

41.  Fornarini, S.; Crestone, E.; Fokin, A. A. The protonation of gaseous cyclopropane. Chem. Eur. J. 2001, 7, 2916–2921.

40.  Schreiner, P. R.; Gunchenko, P. A.; Wittkopp, A.; Yaroshinsky, A. I.; Peleshanko, S. A.; Fokin, A. A.  The rearrangement of the cubane radical cation in solution. Chem. Eur. J. 2001, 7, 2739–2744.

39.  Krasutsky, P. A.; Kolomitsyn, I. V.;  Kiprof, P.;  Carlson, R. M.;  Sydorenko, N. A.; Fokin, A. A.  A Consecutive double-Criegee rearrangement using TFPAA: Stepwise conversion of homoadamantane to oxahomoadamantanes.  J. Org. Chem. 2001, 66, 1701–1707.

38.  Fokin, A. A.; Lauenstein, O.; Gunchenko, P. A.; Schreiner, P. R.  Halogenation of cubane under phase-transfer conditions: Single and double C–H-bond substitution with conservation of the cage Structure.  J. Am. Chem. Soc.  2001, 123, 1842–1847.

37.  Fokin, A. A.; Peleshanko, S. A.; Gunchenko, P. A.; Gusev, D. V.; Schreiner, P. R. Hydrocarbon activations with cerium (IV) ammonium nitrate: Free radical versus oxidative pathways. Eur. J. Org. Chem. 2000, 3357–3362.

36.  Lauenstein, O.; Fokin, A. A.; Schreiner, P. R. A combined experimental and computational study of the H/D kinetic isotope effects for bromination and iodination of aliphatic hydrocarbons under phase-transfer conditions. Org. Lett.  2000, 2201–2204.

35.  Fokin,A. A.;Schreiner,P. R.; Gunchenko, P. A.; Peleshanko, S. A.; Shubina,T. E.; Isaev, S. D.; Tarasenko, P. V.; Kulik, N. I.; Schiebel, H.-M.; YurchenkoA. G. Oxidative single electron transfer activation of s-bonds in aliphatic halogenation reactions. J. Am. Chem. Soc. 2000, 122, 7317–7326.

34.  Fokin, A. A.; Kushko, A. O.; Kirij, A. V.; Yurchenko, A. G.; Schleyer, P. v. R. Direct transformations of ketones to g-unsaturated thiols via [2,3]-sigmatropic rearrangement of allyl sulfinyl carbanions: Combined experimental and theoretical study. J. Org. Chem. 2000, 65, 2984–2995.

33.  Kolomitsin, I. V.; Krasutsky, P. A.; Sidorenko, N. V.; Yurchenko, A. G.; Fokin, A. A.  Oxidative fragmentation of tetrahydrocyclopentadiene structure. Russ. J. Org. Chem. 2000,  36, 456–457.

32.  Krasutsky, P. A.; Kolomitsin, I. V.; Kiprof, P.; Carlson, R. M.; Fokin, A. A. Observation of a stable carbocation in a consecutive Criegee rearrangement with trifluoroperacetic acid. J. Org. Chem. 2000, 65, 3926–3933.

31.  Fokin, A.A.; Kiran, B.; Bremer, M.; Yang, X.; Jiao, H.; Schleyer, P. v. R.  Which electron count rules are needed for four-centered tree-dimensional aromaticity? Chem. Eur. J.; 2000, 6, 1615–1628.

30.  Schreiner, P. R.; Lauenstein, O.; Butova, E. D.; Fokin, A. A. The first efficient iodination of unactivated, aliphatic hydrocarbons. Angew. Chem. 1999, 111 2956–2958. Angew. Chem. Int. Ed. Engl. 1999, 38, 2786–2788. This work is featured: cover picture of the Angewandte Chemie, 1999, issue 18. Chemical and Engineering News 1999 September, 20, 44. Sueddeutsche Zeitung 1999 55, October, 12, p. V2/12.

29.  Fokin, A. A.; Gunchenko, P. A.; Peleshanko, S. A.; Schleyer, P. v. R.; Schreiner, P. R. Common radical cation intermediates in cage hydrocarbon activations.  Eur. J. Org. Chem. 1999, 855–860.

28.  Kushko, A. O.; Yurchenko, A. G.; Kirij, A. V.; Likhotvorik, I. R.; Fokin, A. A.  The novel one-step method of homoallylic tiols synthesis from ketons. Russ. J. Org. Chem. 1998, 34, 776–777.

27.  Fokin, A. A.; Schreiner, P. R.; Schleyer, P. v. R.; Gunchenko, P. A. Electrophilic and oxidative activation of the central C–C Bond in [3.3.n]Propellanes: A theoretical study. J. Org. Chem. 1998,No19, 6494–6502.

26.  Fokin, A. A.; Jiao, H.; Schleyer, P. v. R. From Dodecaheptapentaene to the “[n]Trannulenes”. A new In-plane aromatic family.  J. Am. Chem. Soc. 1998, 120, 9364–9365.

25.  Schreiner, P. R.; Lauenstein, O.; Kolomitsin, I. V.; Fokin, A. A.  Selective C–H activation of aliphatic hydrocarbon under phase-transfer conditions.  Angew. Chem.; Int. Ed. 1998, 37, 1895–1897. This paper was featured in Nachr. Chem. Tech. Lab. 1998 7/8, 706. Chemical and Engineering News 1998 July, 13, 55.

24.  Fokin, A. A.; Gunchenko, P. A.; Tkachenko, B. A.; Butova, E. D.; Yurchenko, A. G.  Backside activation of s-bonds with Cr(VI)-reagents.  Tetrahedron Lett. 1997, 38, 639–642.

23.  Fokin, A. A.; Gunchenko, P. A.; Kulik, N. I.; Iksanova, S. V.; Krasutsky, P. A.; Gogoman, I. V.; Yurchenko, A. G.  NO2+-containing reagents in the electrophilic and oxidative addition to propellanic C–C bond.  Tetrahedron 1996, 52, 5857–5866.

22.  Fokin, A. A.; Gunchenko, P. A.; Krasutsky, P. A.; Yaroshinsky, A. I.; Yurchenko, A. G. Oxidation of tetracyclo[4.3.1.1.4,801,4]undecane (1,4-cyclohomoadamantane). Russ. J. Org. Chem. 1995, 31, 796–797.

21.  Fokin, A. A.; Gunchenko, P. A.; Krasutsky, P. A.; Yaroshinsky, A. I.; Yurchenko, A. G. Oxidative addition to 3,6-dehydrohomoadamantane.  Tetrahedron Lett. 1995, 36, 4479–4482.

20.  Fokin, A. A.; Gagaeva, E. A.; Krasutsky, P. A.; Yurchenko, A. G. Stereoselective epoxidation of 4,7,7-trimethyl-3-oxabicyclo[3.3.1]hept-4-en-2-one. Russ. J. Org. Chem. 1994, 30, 940–941.

19.  Fokin, A. A.; Butova, E. D.; Kolomitsin, I. V.; Gagaeva, E. A.; Kornilov, A. M.; Sorochinsky A. E. Functional derivatives of 2-carene in cyclopropane-containing pyrethroides synthesis. Russ. J. Org. Chem. 1994, 30, 669–679.

18.  Fokin, A. A.; Butova, E. D.; Gulevitch, A. V.; Yurchenko, A. G.; Krasutsky, P. A.  Novel oxidative transformations in norpinonic acid synthesis. Russ. J. Org. Chem. 1993, 29, 1075–1076.

17.  Lichotvorik, I. R.; Litvin, A. L.; Shimko, R. I.; Fokin, A. A. The insertion of dichlorocarbene into tricyclo[5.2.1.02,5]decane structure. Vest. Kiev Polytech. Inst. 1992, 29, 3.

16.  Fokin, A. A.; Krasutsky, P. A.; Gulevich, A.V.; Yurchenko, A. G.  Oxidation of 3,7,7-trimethyl-3,4-dihydroxybicyclo[4.1.0]heptane by molecular oxygen. Russ. J. Org. Chem. 1992, 28, 1098–1099.

15.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structures of 1R-cis-polyhalogenchrysanthemic acids. Russ. J. Org. Chem. 1992, 28, 67–75.

14.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G.  Key synthones of pyrethrinoides based on 3-carene.  Ukr. Khim. Zhurnal 1992, 58, 1130–1135.

13.  Fokin, A. A.; Fedorenko, T. V.; Yurchenko, A. G. Enantioselective synthesis of chrysanthemic acid and derivatives. Ukr. Khim. Zhurnal 1992, 58, 1120–1126.

12.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structure of the stereoisomeric monochlorochrysanthemic acids. Russ. J. Org. Chem. 1991, 27, 1279–1283.

11.  Fokin, A. A.; Krasutsky, P. A.; Baula, O. P.; Yurchenko, A. G.  Functionalization of 4,7,7-trimethyl-3-oxabicyclo[3.31]hept-4-en-2-one with dichlorocarbene. Russ. J. Org. Chem. 1991, 27, 1363.

10.  Krasutsky, P. A.; Fokin, A. A.; Rodionov, V. N.; Kulik, N. I.; Ambrosienko, N. V.; Yurchenko, A. G.  On the mechanisms of transannular acidic cyclization of 3,7-dimethylenobicyclo[3.3.1]nonane and derivatives. Russ. J. Org. Chem. 1991, 27, 992–999.

9.      Krasutsky, P. A.; Fokin, A. A.; Butova, E. D.; Yurchenko, A. G. Stereoselective synthesis of (–)-pirocine and 1R-E-chrysanthemic acid from 2-pinene. Vest. Kiev. Polytech. Inst. 1991, 28, 40–44.

8.      Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G. The structures of carbenilation products of 2-pinene and 3-carene with carboethoxycarbene. Ukr. Khim. Zhurnal 1989, 55,  842–845.

7.      Krasutsky, P. A.; Fokin, A. A.; Maleev, A. V.; Kurkutova, E. N.; Struchkov, Y. T.; Yurchenko, A. G. The structure of adducts of allenes of bicyclo[3.3.1]nonane series with dihalocarbenes. Russ. J. Org. Chem. 1990, 26, 1016–1024.

6.      Krasutsky, P. A.; Fokin, A. A.; Skoba, E. D.; Yurchenko, A. G. the synthesis and protic cyclization of 3-vinylidenobicyclo[3.3.1]nonane-7-one. Russ. J. Org. Chem. 1986, 22, 460–461.

5.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and protic cyclization of 3-vinylideno-7-propadienilidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1986, 22, 459–460.

4.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and reactivity of 3-methylene-7-vinylidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1985, 21, 2522–2626.

3.      Krasutsky, P. A.; Fokin, A. A.; Kulik, N. I.; Yurchenko, A. G. The reactivity of 3,7-divinylidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1985, 21, 2518–2522.

2.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G.; Chekmenyova, L. A. The synthesis of 3,7-divinylidenbicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1984, 20, 1807–1808.

1.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G.; Jones, M. Jr.; Antipin, M. Y.; Struchkov, Y. T. The structure of carbenylation products of 3-methylenebicyclo[3.3.1]nonane. Teoret. i Experim. Khimiya 1984, 20, 427–433. 

 

С) Патенти

 1.      Krasutsky, P. A.; Fokin A. A.; Baula, O. P.; Yurchenko, A.G. The method for obtaining of  (-)-2,2-dimethyl-3-(2-oxopropyl)cyclopropaneacetic acid. USSR patent No 1436451, dated 10.06.1986.

2.      Krasutsky P. A.; Fokin A. A.; Baula O. P.; Krotov V. V.; Yurchenko A.G.  The method for obtaining of 1R-Phenotrine. USSR patent No1583409, dated 08.02.1989.

3.      Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A.G.  The method for obtaining of 1R-cis-2,2-dimethyl-3-(2-chloropropen-1-yl)cyclopropanecarboxylic acid. USSR patent No1684274, dated 18.01.1990.

4.      Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Promonenkov, V.K.  The method of obtaining of methyl esters of 1R-Z-2,2-dimethyl-3-(2-bromopropen-1-yl)cyclopropanecarboxylic acid. USSR patent No1783769, dated 10.04.1990.

5.      Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G.; Dvusherstov, M.G.; Guseva, I.A.; Zhivova, L.V. a-Cyano-3-phenoxybenxylic ester of 1R-cis-2,2-dimethyl-3-(1-bromo-2-chloropropen-1-yl)cyclopropanecarboxylic acid as an insecticide and acaricide. USSR patent No1775397, dated 20.08.1990.

6.      Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G.; Ivanova, G.B.; Sirova, L.M. a-Cyano-3-phenoxybenzylic ester of 1R-cis-2,2-dimethyl-3-(2-chloro-2-acetylvinyl)cyclopro­panecarboxylic acid as insecticide. USSR patent No1766911, dated 20.08.1990.

7.      Fokin, A. A.; Krotov, V. V.; Gunchenko, P. A.; Krasutsky, P.A. The method for obtaining of 1R-cis-2,2-dimethyl-3-(2-oxopropyl)cyclopropanecarboxylic acid. USSR patent No1829332, dated 18.04.1991.

8.      Fokin, A. A.; Butova, E.D.; Gulevich O.V.; Krasutsky, P. A.; Yurchenko, A.G.  The method for obtaining of 1R-cis-2,2-dimethylcyclobutanecarboxylic acid. Ukrainian patent No94061563, dated 06.05.1993.

9.      Peter R. Schreiner, Andrey A. Fokin, Ekaterina D. Butova, Oliver Lauenshtein. Alkaliiodierung. German Patent 19844865, 2000

10.  Schreiner, P. R.; Fokin, A. A.; Wanka, L.; Wolfe, D. Aminoadamantanes and method for producing the same.  German Patent WO/2007/101535. 

11.  Schreiner, P. R.; Fokin, A. A.; Wanka, L.; Wolfe, D. Method for producing 1-formamido-3,5-dimethyladamantane.  German Patent WO/2007/101536.

12.  Schreiner, P. R.; Fokin, A. A. Verfahren zur herstellung von substituirten diamantanen. German Patent WO/2007/065409.

13.  LIU, Zhi; KELLY, Michael, A.; MELOSH, Nicholas, A.; SHEN, Zhi-Xun; FOKIN, Andrey, A.; SCHREINER, Peter, R.; CLAY, Will. PPLICABLE FLUORESCENCE OF DIAMONDOIDS Pub- Number PCT/US2009/000618, International Application No.: WO/2009/099568, Publication Date: 13.08.2009, International Filing Date: 30.01.2009

14.  YANG, Wanli; SHEN, Zhi-Xun; MANOHARAN, Harindran, C.; MELOSH, Nicholas, A.; KELLY, Michael, A.; FOKIN, Andrey, A.; SCHREINER, Peter, R.; RANDEL, Jason, C. OLECULAR RECTIFIERS COMPRISING DIAMONDOIDS Pub. No.: PCT/US2009/000619 International Application No.: WO/2009/099569 Publication Date: 13.08.2009 International Filing Date: 30.01.2009  

15.  Schreiner, P. R.; Fokin, A. A. Method for producing substituted diamantanes. European Patent PCT/DE2006/002146, EP 1960330B1, 02.11.2011

.        Becker, J.; Zhyhadlo, Y. Y.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Ferster, M.; Holthausen, M. C.; Specht, P.; Schindler, S.  Aerobic aliphatic hydroxylation reactions by copper complexes: A simple clipandcleave concept. Chem. Eur. J. 2018, 24, https://doi.org/10.1002/chem.201802607.

158. Gebbie, M. A.; Ishiwata, H.;  McQuade P.J.; Petrak, V.: Taylor, A.; Freiwald, C.; Dahl, J. E.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Nesladek, M.; Melosh, N. A. Experimental measurement of the diamond nucleation landscape reveals classical and nonclassical features. PNAS, 2018, 115, 33, 8284–8289.

157. Moncea, O.; Poinsot, D.; Fokin, A. A.; Schreiner, P. R.; Hierso, J. C. Palladium-catalyzed C2-H arylation of unprotected (N-H)-indoles “On water” using primary diamantyl phosphine oxides as a class of primary phosphine oxide ligands. ChemCatChem, 2018, 10, 2915 – 2922.

154. Yan, H.;Narasimha, K. T.; Denlinger, J.;Li, F. H.;Mo, S.-K.;

153. Yan, H.; Yang, F.; Pan, D.; Lin, Y.; Hohman, J. N.; Solis-Ibarra, D.; Li, F. H.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Galli, G.; Mao, W. L.; Shen Z.-X.; Melosh, N. M. Sterically controlled mechanochemistry under hydrostatic pressure. Nature 2018, 554, 505–510.

152. Gunawan, M. A.; Moncea, O.; Poinsot, D.; Keskes, M.; Domenichini, B.; Heintz, O.; Chassagnon, R.; Herbst, F.; Carlson, R. M. K.; Dahl, J. E. P.; Fokin, A. A.; Schreiner, P. R.; Hierso,  J.-C. Nanodiamond-Palladium Core–Shell Organohybrid Synthesis: A Mild Vapor-Phase Procedure Enabling Nanolayering Metal onto Functionalized sp3-Carbon. Adv. Funct. Mater. 2018, 1705786 (15 p).

151. Gunchenko, P. A.; Li,J.; Liu, B.; Chen, H.; Pashenko, A. P.;Bakhonsky, V. V.; Zhuk. T. S.; Fokin, A. A. Aerobic oxidations with N-hydroxyphthalimide in trifluoroacetic acid. Molec. Cat. 2018, 446, 72-79.

150. Zhyhadlo, Y. Y.; Gaidai, A. V.; Sharapa, D. I.; Mitlenko, A. G.; Shishkin, O. V.; Shishkina, S. V.; Levandovskiy, I. A.; Fokin, A. A. Functionalised Cookson's diketones in chlorosulfonic acid: Towards polysubstituted D3-trishomocubanes. J. Chem. Res. 2017, 41, 12, 677-733.

149. Tyborski, C.; Gillen, R.; Fokin, A. A.; Koso, T. V.; Fokina, N. A.; Hausmann, H.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. Electronic and Vibrational Properties of Diamondoid Oligomers. J. Phys. Chem. 2017, 121, 48, 27082–27088

148. Fokin, A. A.: Zhuk, T. S.; Blomeyer, S.; Peŕez, C.;  Chernish, L.V.; Pashenko, A. E.; Antony, J.; Vishnevskiy, Y. V.;  Berger, R. J. F.; Grimme, S.; Logemann, C.; Schnell, M.; Mitzel N. W.; Schreiner P. R. Intramolecular London dispersion interaction effects on gas-phase and solid-state structures of diamondoid dimers. J. Amer. Chem. Soc. 2017, 139, 16696-16707.

147. Tyborski, C.; Meinke, R.; Gillen, R.; Bischoff, T.; Knecht, A.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N. Schreiner, P. R.; Moller, T.; Rander, T.; Thomsen, C.; Maultzsch, J. From isolated diamondoids to a van-der-Waals crystal: A theoretical and experimental analysis of a trishomocubane and a diamantane dimer in the gas and solid phase. J. Chem. Phys. 2017, 147, 4, 044303 (6 p.)

146. Fokin, A. A.; Pashenko, A. E.; Bakhonsky, V. V.; Zhuk. T. S.; Chernish. L. V.; Gunchenko, P. A.; Kushko, A. O.; Becker, J.; Wende, R. C.; Schreiner. P. R. Chiral building blocks based on 1,2-disubstituted diamantanes. Synthesis, 2017. 49, 2003–2008.

145.     Yan, H.; Hohman, J. N.; Li, F. H.; Jia, C.; Solis-Ibarra, D.; Wu, B.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Vailionis, A.; Kim, T. R.; Devereaux, T. P.; Shen, Z.-X.; Melosh. N. A. Hybrid metal–organic chalcogenide nanowires with electrically conductive inorganic core through diamondoid-directed assembly. Nat. Mater. 2017, 16, 349–355.

144.     Hoc, N. T.;Kushko, A. O.;Fokin, A. A.;Rodionov, V. N. Functional derivatives of diamantanone. Russ. J. Org. Chem. 2016, 52, 8, 1209–1211.

143. Moncea O.; Gunawan, M. A.; Poinsot,D.; Cattey. H.;Becker,J.;Yurchenko,R. I.; Butova,E. D.; Hausmann,H.; Šekutor,M.; Fokin, A. A.; Hierso,J.-C.; Schreiner, P. R. Defying stereotypes with nanodiamonds: Stable primary diamondoid phosphines,  J. Org. Chem. 2016, 81, 8759−8769.

142.     Tverdiy, D. O. Chekanov, M. O.; Savitskiy, P. V.; Syniugin, A. R.; Yarmoliuk, S. M. Fokin, A. A. Efficient preparation of imidazo[1,5-a]pyridine-1-carboxylic acids. Synthesis 2016, 48, A–I.

141.     Ponomarenko, M. V.; Grabowsky,S.; Pal,R.; Röschenthaler, G.-V., Fokin, A. A. SF5-Enolates in Ti(IV)-mediated aldol reactions. J. Org. Chem. 2016, 81, 6783−6791.

140. Karthik, T. N.; Ge,C.; Fabbri,J. D.; Clay,W.; Tkachenko, B. A.; Fokin, A.A.; Schreiner, P. R.; Dahl, J. E.; Carlson, R. M. K.; Shen, Z. X.; Melosh, N. A. Ultra-low effective work function surfaces using diamondoid monolayers. Nature Nanotech. 2016, 11, 267–273.

139. Zhang, J. L.; Ishiwata, H.; Babinec, T. M.; Radulaski, M.; Müller, K.; Lagoudakis, K. G.; Dory, C.; Dahl, J.; Edgington, R.; Soulière, V.; Ferro, G.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N.; Vuckovic, J. Hybrid group IV nanophotonic structures incorporating diamond silicon-vacancy color centers. Nano Lett. 2016, 16, 212−217.

138. Syniugin, A. R.; Chekanov, M. O.; Savitskiy, P. V.; Pashenko, A. E.; Zhuk, T. S.; Yarmoluk, S. M.; Fokin, A A. New method for the synthesis of pyrrolo[2,3-b]dihydroquinolines. Tetrahedron Lett.  2016, 57, 213–215.

137. Valentin, L.; Henss, A.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Becker, S.; Würtele, C.; Schindler, S. Transition metal complexes with cage-opened diamondoid tetracyclo[7.3.1.14,12.02,7]tetradeca-6.11-diene. J. Coor. Chem. 2015, 68, 3295–3301.

136. Lourie, L. F.; Serguchev, Yu. A.; Bentya, A. V.; Ponomarenko, M. V.; Rusanov, E. B.; Vovk, M. V.; Fokin, A. A.; Ignat’ev, N. V. Metal free electrophilic fluoro-cyclization of unsaturated N-hydroxy- and N-acetoxyamides with N–F reagents. J. Fluor. Chem. 2015, 179, 42–47.

135. Bremer, M.; Untenecker, H.; Gunchenko, P. A.; Fokin, A. A.; Schreiner P. R.  Inverted carbon geometries: Challenges to experiment and theory. J. Org. Chem. 2015, 80, 6520−6524.

134. Zhuk, T. S.; Koso, T.; Pashenko, A. E.; Hoc, N. T.; Rodionov, V. N.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Toward an understanding of diamond sp2-defects with unsaturated diamondoid oligomer model. J. Am. Chem. Soc. 2015, 137, 6577−6586.

133. Gunawan, M. A.; Poinsot, D.; Domenichini, B.; Dirand, C.; Chevalier, S.; Fokin, A. A.; Schreiner, P. R.; Hierso, J.-P. The functionalization of nanodiamonds (diamondoids) as a key parameter of their easily controlled self-assembly in micro- and nanocrystals from the vapor phase. Nanoscale, 2015, 7, 1956–1962.

132. Barabash, A. V.; Didukh, N. A.; Kibal’nyi, N. A.; Butova, E. D.; Schreiner, P. R.;Fokin, A. A. Unusual aerobic oxidation of sterically hindered 1-diamanty methyl ketone. Russ. J. Org. Chem. 2014, 50, 1690–1691.

131.       Gunchenko, P. A.; Novikovskii, A. A.; Byk, M. V.; Fokin, A. A.  Structure and transformations of diamantane radical cation: Theory and experiment. Russ. J. Org. Chem. 2014, 50, 1749–1754.

130. Mishura, A. M.; Sklyarova, A. S.; Shamota, T. V.: Rodionov, V. N.; Fokin, A. A.  Preparative synthesis of pentacyclo[6.3.0.02,6.03,10.05,9]undecan-4-one (D3-Trishomocubanone). Russ. J. Org. Chem. 2014, 50, 1542–1544.

129. Barabash, A. V.; Butova, E. D.; Kanyuk, I. M.; Schreiner, P. R.; Fokin, A. A. Beyond the Corey reaction II: Dimethylenation of sterically congested ketones J. Org. Chem. 2014, 79, 10669−10673. ACS Editor’s Choice, 01.10.2014.

128. Randel, J. C.; Niestemski, F. C.; Botello-Mendez, A. R.; Mar, W.; Ndabashimiye, G.; Melinte, S.; Dahl, J. E. P.; Carlson R. M. K.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Charlier, J.-C.; Manoharan, H. C. Unconventional molecule-resolved current rectification in diamondoid fullerene hybrids. Nature Comm. 2014, 5, 4877 (6 p).

127. Tchernobaev, I. I.; Serguchev, Yu. A.; Fokin, A. A. Mechanism and selectivities of the chlorination of toluene in the presence of catalytical composition antimony pentachloride – benzodithio crown ether. Ukr. Krim. Zhurn. 2014, 50, 45–49.

126. Ponomarenko, M. V.; Serguchev, Yu. A.; Hirschberg, M. E.; Röschenthaler, G.-V.; Fokin, A. A. Elemental F2 with transannular dienes: Regioselectivities and mechanisms. Chem. Eur. J. 2014, 20, 10383–10391.

125. Fokin, A.A.; Yurchenko, R. I.; Tkachenko,B.A.; Fokina,N. A.; Gunawan,M. A.; Poinsot,D.; Dahl, J. E. P.; Carlson,R. M. K.; Serafin,M.; Cattey,H.; Hierso,J.-C.; Schreiner, P. R. Selective preparation of diamondoid phosphonates. J. Org. Chem. 2014, 79, 5369–5373.

124. Fokin, A. A.; Zhuk, T. S.; Pashenko, A. E.; Osipov, V. V.; Gunchenko,P. A.; Serafin, M.; Schreiner, P. R. Functionalization of homodiamantane: Oxygen insertion reactions without rearrangement with dimethyldioxirane. J. Org. Chem. 2014, 79, 1861–1866.

123. Meinke, R.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. UV resonance Raman analysis of trishomocubane and diamondoid dimers. J. Chem. Phys. 2014, 140, 034309 (5p).

122. Kahl, P.; Tkachenko, B. A.; Novikovsky, A. A.; Backer, J.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.  Efficient peparation of aically substituted damondoid drivatives, Synthesis 2014, 46, 787–798.

121. Gunawan, M. A.; Hierso, J.-C.; Poinsot, D.; Fokin, A. A.; Fokina, N. A.; Tkachenko, B. A.;Schreiner, P. R. Diamondoids: Functionalization and subsequent applications of perfectly defined molecular cage hydrocarbons. New J. Chem. 2014, 38, 28–41.

120.     Chekanov, M. O.; Ostrynska, O. V.; Tarnavskyi, S. S.; Synyugin, A. R.; Briukhovetska, N. V.; Bdzhola, V. G.; Pashenko, A. E.; Fokin A. A.; Yarmoluk, S. M. Design, synthesis and biological evaluation of 2-aminopyrimidinones and their 6-aza-analogs as a new class of СК2 inhibitors. J. Enz. Inhib. Med. Chem. 2014, 29, 5, 639­–646.

119.     Ponomarenko, M. V.; Lummer, K.; Fokin, A. A.; Serguchev, Yu. A.; Bassil,B. S.; Röschenthaler, G.-V.  Preparations of SF5- and CF3-substituted arenes utilizing the 7-oxabicyclo­[2.2.1]hept-2-ene synthones. Org. Biomol. Chem. 2013, 11, 8103­–8112.

118.     Kacharov, A. D.; Yemets, S. V.; Nemykin,V. N.; Kacharova, L. M.; Fokin,A. A.; Krasutsky, P. A. Stereoselectivity of A-ring contraction for 3-oxotriterpenoids.  RCS Advances 2013, 3, 19057–19063.

117.     Mishura,A. M.; Sklyarova,A. S.; Sharapa, D. I.; Levandovsky, I. A.; Serafin, M.; Fokin, A. A.; Rodionov, V. N. Stereoselective Preparation of mono- and bis-derivatives of pentacyclo[6.3.0.02,6.03,10.05,9]undecane (D3-trishomocubane). Open. Chem.  2013, 11, 2144–2150.

116. Li, F. H.; Fabbri, J. D.; Yurchenko, R. I.; Mileshkin, A. N.; Hohman, J. N.; Yan, H.; Yuan, H.; Tran, I. C.; Willey, T. M.; Bagge-Hansen, M.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N. A. Covalent attachment of diamondoid phosphonic acid dichlorides to tungsten oxide surfaces. Langmuir 2013, 29, 9790–9797.

115. Zimmermann, T.; Richter, R.; Knecht, A.; Fokin, A. A.; Koso, T. V.; Chernish, L. V.; Gunchenko, P. A.; Schreiner, P. R.; Moller, T.; Rander, T. Exploring covalently bound diamondoid aggregates with valence photoelectron spectroscopy. J. Chem. Phys. 2013, 139, 084310 (6 p).

114. Fokin, A. A.; Butova, E. D.; Barabash, A. V; Huu, N. N.; Tkachenko. B. A.; Fokina, N. A.; Schreiner, P. R. Preparative synthesis of vinyl diamondoids. Synth. Comm. 2013, 43, 1772–1777.

113. Sklyarova, A. S.; Rodionov, V. N.; Parsons, C. G.; Quack, G.; Schreiner, P. R.; Fokin, A. A. Preparation and testing of homocubyl amines as therapeutic NMDA receptor antagonists. Med. Chem. Res. 2013, 22, 360–366.

112.     Clay, W. A.; Maldonado, J. R.;  Pianetta, P.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Melosh, N.; Shen, Z.-X. Photocathode device using diamondoid and cesium bromide films Appl. Phys. Lett. 2012, 101, 241605 (5p).

111. Ishiwata, H.; Acremann, Y.; Scholl, A.; Rotenberg, E.; Hellwig, O.; Dobisz, E.; Doran, A.; Tkachenko, B.A.; Fokin, A.A.; Schreiner, P.R.; Dahl, J.E.P.; Carlson, R.M.K.; Melosh, N.; Shen, Z.-X.; Oldag, H. Diamondoid coating enables disruptive approach for chemical and magnetic imaging with 10 nm spatial resolution. Appl. Phys. Lett. 2012, 101, 163101 (5 p).

110. Fokin, A. A.;  Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Hausmann, H.; Serafin, M.; Dahl J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Stable alkanes containing very long carbon–carbon bonds. J. Am. Chem. Soc. 2012, 134, 1364113650.

109. Gunchenko, P. A.; Fokin, A. A. Mechanisms of activation of C–H bonds in framework compounds: Theory and experiment. Theoret. Experim. Khim. 2012, 47, 6, 343–360.

108. Gaidai, A. V.; Volochnyuk, D. M.; Shishkin, O. V.; Fokin, A. A.; Levandovskiy, I. A.; Shubina, T. E. D3-Trishomocubane-4-carboxylic acid as a new chiral building block: Synthesis and absolute configuration. T. E. Synthesis 2012, 44, 810–816.ю

107. Fokina, N. A.; Tkachenko, B. A.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner P. R.  Synthesis of diamondoid carboxylic acid. Synthesis 2012, 44, 259–264.1

106. Fokin, A. A.; Gerbig, D.; Schreiner, P. R. σ/σ- and π/π-Interactions are equally important: multilayered graphanes. J. Am. Chem. Soc. 2011, 133, 20036–20039.

105. Rodionov, V. N.; Sklyarova, A. S.; Shamota, T. V.; Schreiner, P. R.; Fokin, A. A. Selective reductive dimerization of homocubane series oximes. Russ. J. Org. Chem. 2011, 47, 11, 1695−1702.

104.     Schreiner, P. R.; Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Hausmann, H.; Serafin, M.; Schlecht, S.; Dahl J. E. P.; Carlson, R. M. K.; Fokin, A. A. Overcoming  lability of extremely long alkane carbon–carbon bonds through dispersion forces. Nature 2011, 477, 308–311. This paper was featured in Chemical & Engineering News, 89(38), September 19, 2011 [Science & Technology, Concentrates]

103. Novikovskii, A. A.; Gunchenko P. A.; Prikhodchenko P. G.; Serguchev, Yu. A.; Schreiner P. R.; Fokin A.A. Comparative theoretical and experimental analysis of hydrocarbon σ-radical cations. Russ. J. Org. Chem. 2011, 47, 1293–1299.

102.     Shubina, T. E.; Fokin, A. A. Hydrocarbon s-radical cations. WIREs Comput. Mol. Sci. 2011, 1 661679.

101.     Serguchev, Yu. A.; Ponomarenko, M. V.; Lourie, L. F.; Fokin, A. A. Transannular additions of selectfluor and xenon difluoride: regioselectivity and mechanism. J. Phys. Org. Chem. 2011, 24, 407–413.

100.     Butova, E. D.; Barabash, A. V.; Petrova, A. A.; Kleiner, C. M.; Schreiner, P. R.; Fokin. A. A. Stereospecific consecutive epoxide ring expansion with dimethylsulfoxonium methylide, J. Org. Chem. 2010, 75, 18, 6229–6235.

99.    Demchenko, P. Yu.; Gladyshevskii, R. E.; Volkov, S. V.; Kharkova, L. B.; Yanko, O. G.; Fokina, Z. A.; Fokin, A. A. The first nonaselenium ring. Chem. Commun. 2010, 46, 4520–4522.

98.  Lysenko, A. B.; Senchyk, G. A.; Lincke, J.; Lässig, D.; Fokin, A. A.; Butova, E. D.; Schreiner, P. R.; Krautscheid, H.; Domasevitch, K. V. Metal oxide-organic frameworks (MOOFs), a new series of coordination hybrids constructed from molybdenum(VI) oxide and bitopic 1,2,4-triazole linkers. Dalton Trans. 2010, 39, 4223–4231.

97.  Zhuk, T. S.; Bratko, E. Y.; Pashenko, A. E.; Gunchenko, P. A.; Yurchenko, A. G.; Schreiner, P. R.; Fokin, A. A. The “green” synthesis of neuroprotecting drug Memantine. J. Org. Pharm. Chem. 2010, 8, 62–66.

96.  Roth, S.; Leuenberger, D.; Osterwalder, J.; Dahl, J. E.; Carlson, R. M. K.; Tkachenko, B. A. Fokin, A. A.; Schreiner, P. R., Hengsberger, M. Negative-electron-affinity diamondoid monolayers as high-brilliance source for ultrashort electron pulses. Chem. Phys. Lett.  2010, 495, 102–108.

95.  Landt, L.; Bostedt, C.; Wolter, D.; Möller, T.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Kulesza, A.; Bonacic-Koutecky, V. Experimental and theoretical studies of the absorption properties of thiolated diamondoids. J. Chem. Phys. 2010, 132, 144305 (6p).

94.  Landt, L.; Staiger, M.; Wolter, D.; Klünder, K.; Zimmermann, P.; Willey, T. M.; van Buuren, T.; Brehmer, D.; Schreiner, P. R.; Tkachenko, B. A.; Fokin, A. A.; Möller, T.; Bostedt, C. The influence of a single thiol group on the electronic and optical properties of the smallest diamondoid adamantane. J. Chem. Phys. 2010, 132, 0247101(7p).

93.  Levandovskiy, I. A.; Shubina, T. E.; Fokin, A. A. Computational and QSAR study of the alkylnaphthyl ketones adsorption on silver-ion stationary phase.  J. Molec. Mod. 2010, 16, 513–522.

92.  Schreiner, P. R.; Fokin, A. A.; Reisenauer, H. P.;  Tkachenko, B. A.; Vass, E.; Olmstead, M. M.; Bläser, D.; Boese, R.; Dahl, J. E. P.; Carlson, R. M. K. [123]Tetramantane: Parent of a new family of σ-helicenes. J. Am. Chem. Soc. 2009, 131, 11292–11293.

91.  Fokin, A. A.; Gunchenko, P. A.; Novikovsky, A. A.; Shubina, T. E.; Chernyaev, B. V.; Dahl J. E. P.; Carlson, R. M. K.; Yurchenko, A. G.; Schreiner P. R. Photoacetylation of diamondoids: Selectivities and mechanism. Eur. J. Org. Chem. 2009, 5153–5161. This work is featured: Cover picture of the Eur. J. Org. Chem., 2009, issue 30.

90.  Fokin, A. A.; Zhuk, T. S.; Pashenko, A. E.; Dral, P. O.; Gunchenko, P. A.;Dahl, J. E. P.;Carlson, R. M. K.;Koso, T. V.;Serafin, M.; Schreiner, P. R. Oxygen-doped nanodiamonds: Synthesis and functionalizations. Org. Lett. 2009, 11, 3068–3071.

89.  Sklyarova, A. S.; Rodionov, V. N.; Fokin, A. A. A convenient preparative synthesis of pentacyclo[5.3.0.02,5.03,9.04,8]decane (C2-bishomocubane). Russ. J. Org. Chem. 2009, 45, 11, 1644−1647.

88.  Gunchenko, P. A.; Makuhina, A. M.; Novikovsky, A. A.; Yurchenko, A. G.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Structure and transformations of homoadamantane radical cation.  Theoret. and Experim. Khim. 2009, 45, 4, 246–251.

87.  Willey, T. M.; Lee, J. R. I.; Fabbri, J. D.; Wang, D.; Nielsen, M. H.; Randel, J. C.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Dahl, J. E. P.; Carlson, R. M. K.; Terminello, L. J.; Melosh, N. A.; van Buuren, T. Determining orientational structure of diamondoid thiols attached to silver using near-edge X-ray absorption fine structure spectroscopy. J. Elec. Spectr. Rel. Phen. 2009, 172, 69–77.

86.  Schwertfeger, H.; Würtele, C.; Hausmann, H.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R. Selective preparation of diamondoid fluorides. Adv. Synth. Catal. 2009, 351, 1041–1054.

85.  Fokin, A. A.; Schreiner, P. R. Band gap tuning in nanodiamonds: First principle computational studies. Molec. Phys. 2009, 107, 8–12, 823–830.

84.  Fokin, A. A.; Tkachenko, B. A.; Fokina, N.  A.; Hausmann, H.; Serafin, M.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Reactivities of the prism-shaped diamondoids [1(2)3]tetramantane and [12312]hexamantane (cyclohexamantane). Chem. Eur. J. 2009, 15, 3851–3862.

83.  Fokin, A. A.; Merz, A.; Fokina, N. A.; Schwertfeger, H.; Liu, S. L.; Dahl, J. E. P.; Carlson, R. K. M.; Schreiner, P. R.  Synthetic routes to aminotriamantanes, topological analogues of the neuroprotector memantine. Synthesis 2009, 909–912.

82.  Clay, W. A.; Liu, Z.; Yang, W.; Fabbri, J. D.; Dahl, J. E.; Carlson, R. M. K.; Sun, Y.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Pianetta, P. A.; Melosh, N.; Shen Z.-X. Origin of the monochromatic photoemission peak in diamondoid monolayers. Nano Lett. 2009, 9, 57–61.

81.  Willey, T. M.; Fabbri, J. D.; Lee, J. R. I.; Schreiner, P. R.; Fokin, A. A.; Fokina, N. A; Dahl, J. E. P.; Carlson, R. M. K.; Vance, A. L.; Yang, W.; Terminello, L. J.; van Buuren, T.; Melosh, N. A.  Near-edge X-ray absorption fine structure spectroscopy of diamondoid thiol monolayers on gold.  J. Am. Chem. Soc. 2008, 130, 10536–10544.

80.  Chernish, L. V.; Gunchenko, P. A.; Barabash, A. B.; Goreslavets, V. S.; Yurchenko, A. G.; Fokin, A. A. Selective synthesis of 1,1-diadamantane monoderivatives.  Zhurn. Org. Pharm. Khim. 2008, 6, 48–51.

79.  Zhuk, T. S.; Gunchenko, P. A.; Korovai, Ya. Yu.; Schreiner,P. R.; Fokin A. A. Mechanisms of the C–H halogenation of adamantane in the presence of N-hydroxyphthalimide.   Theoret. and Experim. Khim.  2008, 44, 1, 46–51.

78.  Schwertfeger, H; Fokin, A. A.; Schreiner, P. R. Diamonds are a chemist’s best friend: Diamondoid chemistry beyond adamantane.  Angew. Chem. Int. Ed. 2008, 47, 1022–1036.

77.  Fokin, A. A.; Yurchenko, A. G.; Rodionov, V. N.; Gunchenko, P. A.; Yurchenko, R. I.; Reichenberg, A.; Wiesner, J.; Hintz, M.; Jomaa, H.; Schreiner, P.R. Synthesis of the antimalarial drug FR900098 utilizing the nitroso-ene reaction. Org. Lett. 2007, 9, 4379–4382. G

76.  Fokina, N. A.; Tkachenko, B. A.; Merz, A.; Serafin, M.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R. Hydroxy derivatives of diamantane, triamantane, and [121]tetramantane: Selective preparation of bis-apical derivatives. Eur. J. Org. Chem. 2007, 4738–4745.

75.  Butova, E. D.; Fokin, A. A.; Schreiner, P. R. Beyond the Corey reaction: One-Step diolefination of cyclic ketones. J. Org. Chem. 2007, 72, 5689–5696.

74.  Fokin, A. A.; Butova, E. D.; Chernish, L. V.; Fokina, N. A.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Simple preparation of diamondoid 1,3-dienes via oxetane ring opening. Org. Lett. 2007, 9, 2541–2544.0

73.  Yang, W. L.; Fabbri J. D.; Willey, T. M.; Lee, J. R. I.; Dahl, J. E.; Carlson, R. M. K.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Meevasana, W.; Mannella, N.; Tanaka, K.; Zhou, X. J.; van Buuren, T.; Kelly, M. A.; Hussain, Z.; Melosh, N. A.; Shen, Z.-X. Monochromatic electronphotoemission from diamondoid monolayers. Science 2007, 316, 1460–1462.

72.       Wodrich, M. D.; Corminboeuf, C.; Schreiner, P. R.; Fokin, A. A.; Schleyer, P. v. R. How accurate are DFT treatments of organic energies? Org. Lett. 2007, 9, 1851–1854.

71.  Schreiner, P. R.; Fokin, A. A.; Pascal, R. A., Jr.; de Meijere, A. Many density functional theory approaches fail to give reliable large hydrocarbon isomer energy differences. Org. Lett. 2006, 8, 3635–3638.

70.  Fokin, A. A.; Schreiner, P. R.; Fokina, N. A.; Tkachenko, B. A.; Hausmann, H.; Serafin, M. Dahl, J. E. P.; Liu, S.; Carlson, R. M. K.  Functionalized nanodiamonds Part 4: Reactivity of [1(2,3)4]pentamantane (Td-Pentamantane): A nanoscale model of diamond J. Org. Chem. 2006, 71, 8532–8540.

69.   Ponomarenko, M. V.; Serguchev Y. A.; Ponomarenko, B. V.; Röschenthaler, G.-V.; Fokin, A. A. Experimental and theoretical studies on the transannular cyclizations of 3,7-dimethylenebicyclo[3.3.1]nonane with polyfluoroalkyl radicals.  J. Fluor. Chem, 2006, 127, 842–849.

68.  Schreiner, P. R.; Fokina, N. A.; Tkachenko, B. A.; Hausmann, H.; Serafin, M.; Dahl, J. E. P.; Liu, S.; Carlson, R. M. K.; Fokin, A. A. Functionalized Nanodiamonds Part 2: Triamantane and [121]Tetramantane. J. Org. Chem. 2006, 71, 18, 6709–6720. This work is featured: Cover picture of the J. Org. Chem., 2006, issue 18.

67.  Tkachenko, B. A.; Fokina, N. A.; Chernish, L. V.; Dahl, J. E. P.; Liu, S.; Carlson, M. K.; Fokin, A. A.; Schreiner, P. R. Functionalized Nanodiamonds Part 3: Thiolation of tertiary/bridgehead alcohols. Org. Lett. 2006, 8, 1767–1770.

66.  Fokin, A. A.; Schreiner, P. R.; Berger, R.; Robinson, G. H.; Wei, P.; Campana, C. F. Pseudotetrahedral polyhalocubanes: Synthesis, structures, and parity violating energy differences. J. Am. Chem. Soc. 2006, 128, 5332–5333. This work is featured: Nature, 2006, 44, 4, 5.

65.  Fokin, A. A.; Tkachenko, B. A.; Gunchenko, P. A. Gusev, D. V. Schreiner, P. R. Functionalized Nanodiamonds Part I. An experimental assessment of diamantane and computational predictions for higher diamondoids. Chem. Eur. J. 2005, 11, 7091–7101.

64.  de Meijere, A.; Lee, C.-H.; Kuznetsov M. A.; Gusev, D. V.; Kozhushkov, S. I.; Fokin, A. A.; Schreiner, P. R. Preparation and reactivity of [D3d]-octahedrane: The most stable (CH)12 hydrocarbon. Chem. Eur. J. 2005, 11, 6175–6184.

63.  Rodionov, V. N.; Chernyaev, B. V.; Levandovskii, I. A.; Shubina, T. E.; Fokin, A. A..  Quantum-chemical interpretation of the reorientation of dialkyl-cis-9,10-dihydroanthracene-9,10-endofumarates on a silver-containing stationary phase.  Theoret. and Experim. Khim. 2005, 41, 1, 1–6.

62.  Rodionov, V. M.; Chernyaev, B. V.; Levandovs'kii, I. A.; Shubina, T. E.; Fokin, A. A.; Yurchenko, O. G.  Experimental and quantum-chemical study of the thermodynamics of complexation of methylbenzenes with silver(I) ion.          Naukovi Visti - Natsional'nii Tekhnichnii Universitet Ukraini "Kiivs'kii Politekhnichnii Institut"  2005, 1, 107–115.

61.  Fokin, A. A.; Tkachenko, B. A.; Gunchenko, P. A.; Schreiner, P. R. The protonation of cubane revisited. Angew. Chem. Int. Ed. 2005, 44, 146–149.

60.  Schreiner, P. R.; Fokin, A. A.; Kotke, M.; Weil, T. Noncovalent organocatalysis.  Ann. Pol. Chem. Soc. 2004, 3, part 1, 21–24.

59.  Schreiner, P. R.; Fokin, A. A. Selective alkane C–H-bond functionalizations utilizing oxidative single-electron transfer and organocatalysis. Chem. Record 2004, 3, 247–257.

58.  Kiriy, N.; Jahne, E.; Adler, H.-J.; Schneider, M.; Kiriy, A.; Gorodyska, G.; Minko, S.; Jehnichen, D.; Simon,|P.; Fokin, A. A.; Stamm, M. One-dimensional aggregation of regioregular polyalkylthiophenes. Nano Letters 2003, 3, 707–712.

57.  Gunchenko, P. A.; Vigovskaya, T. S.; Fokin, A. A.; Yurchenko, A. G. A New method for building of [3.3.3]propellan skeleton.  Ukr. Khim. Zhurn. 2003, 69, 10, 113–115.

56.  Fokin, A. A.; Schreiner, P. R. Metal-free, selective alkane functionalizations.  Adv. Chem. Cat. 2003, 345, 1035–1052.

55.  de Meijere, A.; Kozhushkov, S. I.; Fokin, A. A.; Emme, I.; Redlich, S.; Schreiner, P. R. New structurally interesting cyclopropane derivatives. A world of wonders and surprises. Pure Appl. Chem. 2003, 75, 549–562.

54.  Fokin, A. A.; Schreiner, P. R.; Kozhushkov, S. I.; Sattelmeyer, K. W.; Schaefer, H. F.; de Meijere, A. Delocalizations in s-radical cations: The Intriguing structures of ionized [n]rotanes.  Org. Lett. 2003, 5, 697–700.

53.  Tkachenko, B. A.; Shubina, T. E.; Gusev, D. V.; Gunchenko, P. A.; Yurchenko, A. G.; Schreiner, P. R.; Fokin, A. A. Mechanisms of C–H Activation of Alkanes by Chromium-oxo Reagents.  Theoret. and Experim. Khim. 2003, 39, 2, 90–95.

52.   Krasutsky, P. A.; Kolomitsyn, I. V.; Botov, E. M.; Carlson, R. M.; Semenova, I. G.; Fokin, A. A. Heterolytic decarboxylation involving acyltrifluoroacetyl peroxide intermediates. Tetrahedron Lett. 2002, 43, 8687–8691.

51.  Schreiner, P. R.; Fokin, A. A.; Lauenstein, O.;  Okamoto, Y.; Wakita, T.; Rinderspacher, C; Robinson, G. H.; Vohs, J. K.; Campana.; C. F. Pseudotetrahedral polyhaloadamantanes as chirality probes: Synthesis, separation, and absolute configuration.  J. Am. Chem. Soc. 2002, 124, 13348–13349.

50.  Fokin, A. A.; Tkachenko, B. A.; Shubina, T. E.; Gunchenko, P. A.; Gusev, D. V.; Vohs, J. K.; Robinson, R. H.; Yurchenko, A. G.; Schreiner, P. R. The protoadamantane radical cation.  Eur. J. Org. Chem. 2002, 3844–3849.

49.  Shubina, T. E.; Gunchenko, P. A.; Vigovskaya, T. S.; Schreiner, P. R.; Yurchenko, A. G.; Fokin, A. A.  [3.3.2]- and [3.3.3]propellanes in reactions with oxidizing electrophiles. Teoret. i Experim. Khimiya, 2002, 38, 4, 226–231.

46.  Kiriy, A. V.; Yurchenko, A. G.; Fokin, A. A. The new [2,3]-sigmatropic rearrangement of allylsulfinyl carbanions. Russ. J. Org. Chem. 2002, 38, 3, 471–472.

48.  Fokin, A. A.; Shubina, T. E.; Gunchenko, P. A.; Isaev, S. D.; Yurchenko, A. G.; Schreiner, P. R. H-Coupled electron transfer in alkane C–H activations with halogen electrophiles. J. Am. Chem. Soc. 2002, 124, 10718–10727.

47.  Fokin, A. A.; Schreiner, P. R. Selective alkane transformations via radicals and radical cations: Insights into the activation step from experiment and theory. Chem. Rev. 2002, 102, 1551–1593.

45.  Shubina, T. E.; Gunchenko. P. A.; Yurchenko, A. G.; Schreiner, P. R.; Butova, E. D.; Fokin, A. A. Structure and transformations of 1-alkyladamantane radical cations.  Teoret. i Experim. Khimiya 2002, 38, 1, 8–13.

44.  Schreiner, P. R.; Lauenstein, O.; Butova, E. D.; Gunchenko, P. V.; Kolomitsin, I. V.; Wittkopp, A.; Feder, G.; Fokin, A. A. Selective radical reactions in multiphase systems: Phase-transfer halogenations of alkanes. Chem. Eur. J. 2001, 7, 23, 4996–5003.

43.  Fokin, A. A.; Tkachenko, B. A.; Korshunov, O. I.; Gunchenko, P. A.; Schreiner, P. R. Molecule-induced alkane homolysis with dioxiranes. J. Am. Chem. Soc. 2001, 123, 11248–11252.

42.  Prall, M.; Wittkopp, A.; Fokin, A. A.; Schreiner, P. R.  Substituent effects on the Bergman Cyclization of (Z)-1,5-hexadiyne-3-enes: A systematic computational study. J. Comp. Chem. 2001, 22, 13, 1605–1614.

41.  Fornarini, S.; Crestone, E.; Fokin, A. A. The protonation of gaseous cyclopropane. Chem. Eur. J. 2001, 7, 2916–2921.

40.  Schreiner, P. R.; Gunchenko, P. A.; Wittkopp, A.; Yaroshinsky, A. I.; Peleshanko, S. A.; Fokin, A. A.  The rearrangement of the cubane radical cation in solution. Chem. Eur. J. 2001, 7, 2739–2744.

39.  Krasutsky, P. A.; Kolomitsyn, I. V.;  Kiprof, P.;  Carlson, R. M.;  Sydorenko, N. A.; Fokin, A. A.  A Consecutive double-Criegee rearrangement using TFPAA: Stepwise conversion of homoadamantane to oxahomoadamantanes.  J. Org. Chem. 2001, 66, 1701–1707.

38.  Fokin, A. A.; Lauenstein, O.; Gunchenko, P. A.; Schreiner, P. R.  Halogenation of cubane under phase-transfer conditions: Single and double C–H-bond substitution with conservation of the cage Structure.  J. Am. Chem. Soc.  2001, 123, 1842–1847.

37.  Fokin, A. A.; Peleshanko, S. A.; Gunchenko, P. A.; Gusev, D. V.; Schreiner, P. R. Hydrocarbon activations with cerium (IV) ammonium nitrate: Free radical versus oxidative pathways. Eur. J. Org. Chem. 2000, 3357–3362.

36.  Lauenstein, O.; Fokin, A. A.; Schreiner, P. R. A combined experimental and computational study of the H/D kinetic isotope effects for bromination and iodination of aliphatic hydrocarbons under phase-transfer conditions. Org. Lett.  2000, 2201–2204.

35.  Fokin,A. A.;Schreiner,P. R.; Gunchenko, P. A.; Peleshanko, S. A.; Shubina,T. E.; Isaev, S. D.; Tarasenko, P. V.; Kulik, N. I.; Schiebel, H.-M.; YurchenkoA. G. Oxidative single electron transfer activation of s-bonds in aliphatic halogenation reactions. J. Am. Chem. Soc. 2000, 122, 7317–7326.

34.  Fokin, A. A.; Kushko, A. O.; Kirij, A. V.; Yurchenko, A. G.; Schleyer, P. v. R. Direct transformations of ketones to g-unsaturated thiols via [2,3]-sigmatropic rearrangement of allyl sulfinyl carbanions: Combined experimental and theoretical study. J. Org. Chem. 2000, 65, 2984–2995.

33.  Kolomitsin, I. V.; Krasutsky, P. A.; Sidorenko, N. V.; Yurchenko, A. G.; Fokin, A. A.  Oxidative fragmentation of tetrahydrocyclopentadiene structure. Russ. J. Org. Chem. 2000,  36, 456–457.

32.  Krasutsky, P. A.; Kolomitsin, I. V.; Kiprof, P.; Carlson, R. M.; Fokin, A. A. Observation of a stable carbocation in a consecutive Criegee rearrangement with trifluoroperacetic acid. J. Org. Chem. 2000, 65, 3926–3933.

31.  Fokin, A.A.; Kiran, B.; Bremer, M.; Yang, X.; Jiao, H.; Schleyer, P. v. R.  Which electron count rules are needed for four-centered tree-dimensional aromaticity? Chem. Eur. J.; 2000, 6, 1615–1628.

30.  Schreiner, P. R.; Lauenstein, O.; Butova, E. D.; Fokin, A. A. The first efficient iodination of unactivated, aliphatic hydrocarbons. Angew. Chem. 1999, 111 2956–2958. Angew. Chem. Int. Ed. Engl. 1999, 38, 2786–2788. This work is featured: cover picture of the Angewandte Chemie, 1999, issue 18. Chemical and Engineering News 1999 September, 20, 44. Sueddeutsche Zeitung 1999 55, October, 12, p. V2/12.

29.  Fokin, A. A.; Gunchenko, P. A.; Peleshanko, S. A.; Schleyer, P. v. R.; Schreiner, P. R. Common radical cation intermediates in cage hydrocarbon activations.  Eur. J. Org. Chem. 1999, 855–860.

28.  Kushko, A. O.; Yurchenko, A. G.; Kirij, A. V.; Likhotvorik, I. R.; Fokin, A. A.  The novel one-step method of homoallylic tiols synthesis from ketons. Russ. J. Org. Chem. 1998, 34, 776–777.

27.  Fokin, A. A.; Schreiner, P. R.; Schleyer, P. v. R.; Gunchenko, P. A. Electrophilic and oxidative activation of the central C–C Bond in [3.3.n]Propellanes: A theoretical study. J. Org. Chem. 1998,No19, 6494–6502.

26.  Fokin, A. A.; Jiao, H.; Schleyer, P. v. R. From Dodecaheptapentaene to the “[n]Trannulenes”. A new In-plane aromatic family.  J. Am. Chem. Soc. 1998, 120, 9364–9365.

25.  Schreiner, P. R.; Lauenstein, O.; Kolomitsin, I. V.; Fokin, A. A.  Selective C–H activation of aliphatic hydrocarbon under phase-transfer conditions.  Angew. Chem.; Int. Ed. 1998, 37, 1895–1897. This paper was featured in Nachr. Chem. Tech. Lab. 1998 7/8, 706. Chemical and Engineering News 1998 July, 13, 55.

24.  Fokin, A. A.; Gunchenko, P. A.; Tkachenko, B. A.; Butova, E. D.; Yurchenko, A. G.  Backside activation of s-bonds with Cr(VI)-reagents.  Tetrahedron Lett. 1997, 38, 639–642.

23.  Fokin, A. A.; Gunchenko, P. A.; Kulik, N. I.; Iksanova, S. V.; Krasutsky, P. A.; Gogoman, I. V.; Yurchenko, A. G.  NO2+-containing reagents in the electrophilic and oxidative addition to propellanic C–C bond.  Tetrahedron 1996, 52, 5857–5866.

22.  Fokin, A. A.; Gunchenko, P. A.; Krasutsky, P. A.; Yaroshinsky, A. I.; Yurchenko, A. G. Oxidation of tetracyclo[4.3.1.1.4,801,4]undecane (1,4-cyclohomoadamantane). Russ. J. Org. Chem. 1995, 31, 796–797.

21.  Fokin, A. A.; Gunchenko, P. A.; Krasutsky, P. A.; Yaroshinsky, A. I.; Yurchenko, A. G. Oxidative addition to 3,6-dehydrohomoadamantane.  Tetrahedron Lett. 1995, 36, 4479–4482.

20.  Fokin, A. A.; Gagaeva, E. A.; Krasutsky, P. A.; Yurchenko, A. G. Stereoselective epoxidation of 4,7,7-trimethyl-3-oxabicyclo[3.3.1]hept-4-en-2-one. Russ. J. Org. Chem. 1994, 30, 940–941.

19.  Fokin, A. A.; Butova, E. D.; Kolomitsin, I. V.; Gagaeva, E. A.; Kornilov, A. M.; Sorochinsky A. E. Functional derivatives of 2-carene in cyclopropane-containing pyrethroides synthesis. Russ. J. Org. Chem. 1994, 30, 669–679.

18.  Fokin, A. A.; Butova, E. D.; Gulevitch, A. V.; Yurchenko, A. G.; Krasutsky, P. A.  Novel oxidative transformations in norpinonic acid synthesis. Russ. J. Org. Chem. 1993, 29, 1075–1076.

17.  Lichotvorik, I. R.; Litvin, A. L.; Shimko, R. I.; Fokin, A. A. The insertion of dichlorocarbene into tricyclo[5.2.1.02,5]decane structure. Vest. Kiev Polytech. Inst. 1992, 29, 3.

16.  Fokin, A. A.; Krasutsky, P. A.; Gulevich, A.V.; Yurchenko, A. G.  Oxidation of 3,7,7-trimethyl-3,4-dihydroxybicyclo[4.1.0]heptane by molecular oxygen. Russ. J. Org. Chem. 1992, 28, 1098–1099.

15.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structures of 1R-cis-polyhalogenchrysanthemic acids. Russ. J. Org. Chem. 1992, 28, 67–75.

14.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G.  Key synthones of pyrethrinoides based on 3-carene.  Ukr. Khim. Zhurnal 1992, 58, 1130–1135.

13.  Fokin, A. A.; Fedorenko, T. V.; Yurchenko, A. G. Enantioselective synthesis of chrysanthemic acid and derivatives. Ukr. Khim. Zhurnal 1992, 58, 1120–1126.

12.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structure of the stereoisomeric monochlorochrysanthemic acids. Russ. J. Org. Chem. 1991, 27, 1279–1283.

11.  Fokin, A. A.; Krasutsky, P. A.; Baula, O. P.; Yurchenko, A. G.  Functionalization of 4,7,7-trimethyl-3-oxabicyclo[3.31]hept-4-en-2-one with dichlorocarbene. Russ. J. Org. Chem. 1991, 27, 1363.

10.  Krasutsky, P. A.; Fokin, A. A.; Rodionov, V. N.; Kulik, N. I.; Ambrosienko, N. V.; Yurchenko, A. G.  On the mechanisms of transannular acidic cyclization of 3,7-dimethylenobicyclo[3.3.1]nonane and derivatives. Russ. J. Org. Chem. 1991, 27, 992–999.

9.      Krasutsky, P. A.; Fokin, A. A.; Butova, E. D.; Yurchenko, A. G. Stereoselective synthesis of (–)-pirocine and 1R-E-chrysanthemic acid from 2-pinene. Vest. Kiev. Polytech. Inst. 1991, 28, 40–44.

8.      Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G. The structures of carbenilation products of 2-pinene and 3-carene with carboethoxycarbene. Ukr. Khim. Zhurnal 1989, 55,  842–845.

7.      Krasutsky, P. A.; Fokin, A. A.; Maleev, A. V.; Kurkutova, E. N.; Struchkov, Y. T.; Yurchenko, A. G. The structure of adducts of allenes of bicyclo[3.3.1]nonane series with dihalocarbenes. Russ. J. Org. Chem. 1990, 26, 1016–1024.

6.      Krasutsky, P. A.; Fokin, A. A.; Skoba, E. D.; Yurchenko, A. G. the synthesis and protic cyclization of 3-vinylidenobicyclo[3.3.1]nonane-7-one. Russ. J. Org. Chem. 1986, 22, 460–461.

5.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and protic cyclization of 3-vinylideno-7-propadienilidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1986, 22, 459–460.

4.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and reactivity of 3-methylene-7-vinylidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1985, 21, 2522–2626.

3.      Krasutsky, P. A.; Fokin, A. A.; Kulik, N. I.; Yurchenko, A. G. The reactivity of 3,7-divinylidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1985, 21, 2518–2522.

2.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G.; Chekmenyova, L. A. The synthesis of 3,7-divinylidenbicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1984, 20, 1807–1808.

1.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G.; Jones, M. Jr.; Antipin, M. Y.; Struchkov, Y. T. The structure of carbenylation products of 3-methylenebicyclo[3.3.1]nonane. Teoret. i Experim. Khimiya 1984, 20, 427–433.

 

159. Becker, J.; Zhyhadlo, Y. Y.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Ferster, M.; Holthausen, M. C.; Specht, P.; Schindler, S.  Aerobic aliphatic hydroxylation reactions by copper complexes: A simple clipandcleave concept. Chem. Eur. J.2018, 24, https://doi.org/10.1002/chem.201802607

158.Gebbie, M. A.; Ishiwata, H.;  McQuade P.J.; Petrak, V.: Taylor, A.; Freiwald, C.; Dahl, J. E.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Nesladek, M.; Melosh, N. A. Experimental measurement of the diamond nucleation landscape reveals classical and nonclassical features. PNAS, 2018, 115, 33, 8284–8289.

157. Moncea, O.; Poinsot, D.; Fokin, A. A.; Schreiner, P. R.; Hierso, J. C. Palladium-catalyzed C2-H arylation of unprotected (N-H)-indoles “On water” using primary diamantyl phosphine oxides as a class of primary phosphine oxide ligands. ChemCatChem, 2018, 10, 2915 – 2922.

155.Hoc, N. T.  Fokin, A. A; Rodionov, V. N. Towards 3-(2-adamantylidene)diamantane derivatives through the McMurry cross coupling reaction. Org. Commun. 2018, 11, 2x, 75-79.

156. Hoc, N. T.  Fokin, A. A; Rodionov, V. N. Synthesis of 10-methoxydiamantan-3-one. MOLBANK. 2018, 2, UNSP M990. DOI: 10.3390/M990

154.Yan, H.;Narasimha, K. T.; Denlinger, J.;Li, F. H.;Mo, S.-K.;Nathan Hohman, J.;  Dahl, J. E. P.; ,Carlson, R. M. K.;Tkachenko, B. A.;Fokin, A. A.; Schreiner, P. R.; Hussain, Z.; Shen, Z.-X.; ,Melosh, N. A.Monochromatic photocathodes from graphene-stabilized diamondoids. Nano Lett., 2018, 18, 1099–1103.

153.Yan, H.; Yang, F.; Pan, D.; Lin, Y.; Hohman, J. N.; Solis-Ibarra, D.; Li, F. H.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Galli, G.; Mao, W. L.; Shen Z.-X.; Melosh, N. M. Sterically controlled mechanochemistry under hydrostatic pressure. Nature 2018, 554, 505–510.

152.Gunawan, M. A.; Moncea, O.; Poinsot, D.; Keskes, M.; Domenichini, B.; Heintz, O.; Chassagnon, R.; Herbst, F.; Carlson, R. M. K.; Dahl, J. E. P.; Fokin, A. A.; Schreiner, P. R.; Hierso,  J.-C. Nanodiamond-Palladium Core–Shell Organohybrid Synthesis: A Mild Vapor-Phase Procedure Enabling Nanolayering Metal onto Functionalized sp3-Carbon. Adv. Funct. Mater. 2018, 1705786 (15 p).

151.Gunchenko, P. A.; Li,J.; Liu, B.; Chen, H.; Pashenko, A. P.;Bakhonsky, V. V.; Zhuk. T. S.; Fokin, A. A. Aerobic oxidations with N-hydroxyphthalimide in trifluoroacetic acid. Molec. Cat. 2018, 446, 72-79.

150.Zhyhadlo, Y. Y.; Gaidai, A. V.; Sharapa, D. I.; Mitlenko, A. G.; Shishkin, O. V.; Shishkina, S. V.; Levandovskiy, I. A.; Fokin, A. A. Functionalised Cookson's diketones in chlorosulfonic acid: Towards polysubstituted D3-trishomocubanes. J. Chem. Res. 2017, 41, 12, 677-733.

149.Tyborski, C.; Gillen, R.; Fokin, A. A.; Koso, T. V.; Fokina, N. A.; Hausmann, H.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. Electronic and Vibrational Properties of Diamondoid Oligomers. J. Phys. Chem. 2017, 121, 48, 27082–27088

148.     Fokin, A. A.: Zhuk, T. S.; Blomeyer, S.; Peŕez, C.;  Chernish, L.V.; Pashenko, A. E.; Antony, J.; Vishnevskiy, Y. V.;  Berger, R. J. F.; Grimme, S.; Logemann, C.; Schnell, M.; Mitzel N. W.; Schreiner P. R. Intramolecular London dispersion interaction effects on gas-phase and solid-state structures of diamondoid dimers. J. Amer. Chem. Soc. 2017, 139, 16696-16707.

147.     Tyborski, C.; Meinke, R.; Gillen, R.; Bischoff, T.; Knecht, A.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N. Schreiner, P. R.; Moller, T.; Rander, T.; Thomsen, C.; Maultzsch, J. From isolated diamondoids to a van-der-Waals crystal: A theoretical and experimental analysis of a trishomocubane and a diamantane dimer in the gas and solid phase. J. Chem. Phys. 2017, 147, 4, 044303 (6 p.)

146.     Fokin, A. A.; Pashenko, A. E.; Bakhonsky, V. V.; Zhuk. T. S.; Chernish. L. V.; Gunchenko, P. A.; Kushko, A. O.; Becker, J.; Wende, R. C.; Schreiner. P. R. Chiral building blocks based on 1,2-disubstituted diamantanes. Synthesis, 2017. 49, 20032008.

145.     Yan, H.; Hohman, J. N.; Li, F. H.; Jia, C.; Solis-Ibarra, D.; Wu, B.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Vailionis, A.; Kim, T. R.; Devereaux, T. P.; Shen, Z.-X.; Melosh. N. A. Hybrid metal–organic chalcogenide nanowires with electrically conductive inorganic core through diamondoid-directed assembly. Nat. Mater. 2017, 16, 349–355.

144.  Hoc, N. T.;Kushko, A. O.;Fokin, A. A.;Rodionov, V. N. Functional derivatives of diamantanone. Russ. J. Org. Chem. 2016, 52, 8, 1209–1211.

143.Moncea O.; Gunawan, M. A.; Poinsot,D.; Cattey. H.;Becker,J.;Yurchenko,R. I.; Butova,E. D.; Hausmann,H.; Šekutor,M.; Fokin, A. A.; Hierso,J.-C.; Schreiner, P. R. Defying stereotypes with nanodiamonds: Stable primary diamondoid phosphines,  J. Org. Chem. 2016, 81, 8759−8769.

142.     Tverdiy, D. O. Chekanov, M. O.; Savitskiy, P. V.; Syniugin, A. R.; Yarmoliuk, S. M. Fokin, A. A. Efficient preparation of imidazo[1,5-a]pyridine-1-carboxylic acids. Synthesis 2016, 48, A–I.

141.     Ponomarenko, M. V.; Grabowsky,S.; Pal,R.; Röschenthaler, G.-V., Fokin, A. A. SF5-Enolates in Ti(IV)-mediated aldol reactions. J. Org. Chem. 2016, 81, 6783−6791.

140.     Karthik, T. N.; Ge,C.; Fabbri,J. D.; Clay,W.; Tkachenko, B. A.; Fokin, A.A.; Schreiner, P. R.; Dahl, J. E.; Carlson, R. M. K.; Shen, Z. X.; Melosh, N. A. Ultra-low effective work function surfaces using diamondoid monolayers. Nature Nanotech. 2016, 11, 267–273.

139.     Zhang, J. L.; Ishiwata, H.; Babinec, T. M.; Radulaski, M.; Müller, K.; Lagoudakis, K. G.; Dory, C.; Dahl, J.; Edgington, R.; Soulière, V.; Ferro, G.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N.; Vuckovic, J. Hybrid group IV nanophotonic structures incorporating diamond silicon-vacancy color centers. Nano Lett. 2016, 16, 212−217.

138.Syniugin, A. R.; Chekanov, M. O.; Savitskiy, P. V.; Pashenko, A. E.; Zhuk, T. S.; Yarmoluk, S. M.; Fokin, A A. New method for the synthesis of pyrrolo[2,3-b]dihydroquinolines. Tetrahedron Lett.  2016, 57, 213–215.

137.Valentin, L.; Henss, A.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Becker, S.; Würtele, C.; Schindler, S. Transition metal complexes with cage-opened diamondoid tetracyclo[7.3.1.14,12.02,7]tetradeca-6.11-diene. J. Coor. Chem. 2015, 68, 3295–3301.

136.Lourie, L. F.; Serguchev, Yu. A.; Bentya, A. V.; Ponomarenko, M. V.; Rusanov, E. B.; Vovk, M. V.; Fokin, A. A.; Ignat’ev, N. V. Metal free electrophilic fluoro-cyclization of unsaturated N-hydroxy- and N-acetoxyamides with N–F reagents. J. Fluor. Chem. 2015, 179, 42–47.

135.Bremer, M.; Untenecker, H.; Gunchenko, P. A.; Fokin, A. A.; Schreiner P. R.  Inverted carbon geometries: Challenges to experiment and theory. J. Org. Chem. 2015, 80, 6520−6524.

134.     Zhuk, T. S.; Koso, T.; Pashenko, A. E.; Hoc, N. T.; Rodionov, V. N.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Toward an understanding of diamond sp2-defects with unsaturated diamondoid oligomer model. J. Am. Chem. Soc. 2015, 137, 6577−6586.

133.     Gunawan, M. A.; Poinsot, D.; Domenichini, B.; Dirand, C.; Chevalier, S.; Fokin, A. A.; Schreiner, P. R.; Hierso, J.-P. The functionalization of nanodiamonds (diamondoids) as a key parameter of their easily controlled self-assembly in micro- and nanocrystals from the vapor phase. Nanoscale, 2015, 7, 1956–1962.

132.     Barabash, A. V.; Didukh, N. A.; Kibal’nyi, N. A.; Butova, E. D.; Schreiner, P. R.;Fokin, A. A. Unusual aerobic oxidation of sterically hindered 1-diamanty methyl ketone. Russ. J. Org. Chem. 2014, 50, 1690–1691.

131.       Gunchenko, P. A.; Novikovskii, A. A.; Byk, M. V.; Fokin, A. A.  Structure and transformations of diamantane radical cation: Theory and experiment. Russ. J. Org. Chem. 2014, 50, 1749–1754.

130.Mishura, A. M.; Sklyarova, A. S.; Shamota, T. V.: Rodionov, V. N.; Fokin, A. A.  Preparative synthesis of pentacyclo[6.3.0.02,6.03,10.05,9]undecan-4-one (D3-Trishomocubanone). Russ. J. Org. Chem. 2014, 50, 1542–1544.

129.Barabash, A. V.; Butova, E. D.; Kanyuk, I. M.; Schreiner, P. R.; Fokin, A. A. Beyond the Corey reaction II: Dimethylenation of sterically congested ketones J. Org. Chem. 2014, 79, 10669−10673. ACS Editor’s Choice, 01.10.2014.

128.Randel, J. C.; Niestemski, F. C.; Botello-Mendez, A. R.; Mar, W.; Ndabashimiye, G.; Melinte, S.; Dahl, J. E. P.; Carlson R. M. K.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Charlier, J.-C.; Manoharan, H. C. Unconventional molecule-resolved current rectification in diamondoid fullerene hybrids. Nature Comm. 2014, 5, 4877 (6 p).

127.Tchernobaev, I. I.; Serguchev, Yu. A.; Fokin, A. A. Mechanism and selectivities of the chlorination of toluene in the presence of catalytical composition antimony pentachloride – benzodithio crown ether. Ukr. Krim. Zhurn. 2014, 50, 45–49.

126.Ponomarenko, M. V.; Serguchev, Yu. A.; Hirschberg, M. E.; Röschenthaler, G.-V.; Fokin, A. A. Elemental F2 with transannular dienes: Regioselectivities and mechanisms. Chem. Eur. J. 2014, 20, 10383–10391.

125.Fokin, A.A.; Yurchenko, R. I.; Tkachenko,B.A.; Fokina,N. A.; Gunawan,M. A.; Poinsot,D.; Dahl, J. E. P.; Carlson,R. M. K.; Serafin,M.; Cattey,H.; Hierso,J.-C.; Schreiner, P. R. Selective preparation of diamondoid phosphonates. J. Org. Chem. 2014, 79, 5369–5373.

124.Fokin, A. A.; Zhuk, T. S.; Pashenko, A. E.; Osipov, V. V.; Gunchenko,P. A.; Serafin, M.; Schreiner, P. R. Functionalization of homodiamantane: Oxygen insertion reactions without rearrangement with dimethyldioxirane. J. Org. Chem. 2014, 79, 1861–1866.

123.Meinke, R.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. UV resonance Raman analysis of trishomocubane and diamondoid dimers. J. Chem. Phys. 2014, 140, 034309 (5p).

122.Kahl, P.; Tkachenko, B. A.; Novikovsky, A. A.; Backer, J.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.  Efficient peparation of aically substituted damondoid drivatives, Synthesis 2014, 46, 787–798.

121.Gunawan, M. A.; Hierso, J.-C.; Poinsot, D.; Fokin, A. A.; Fokina, N. A.; Tkachenko, B. A.;Schreiner, P. R. Diamondoids: Functionalization and subsequent applications of perfectly defined molecular cage hydrocarbons. New J. Chem. 2014, 38, 28–41.

120.     Chekanov, M. O.; Ostrynska, O. V.; Tarnavskyi, S. S.; Synyugin, A. R.; Briukhovetska, N. V.; Bdzhola, V. G.; Pashenko, A. E.; Fokin A. A.; Yarmoluk, S. M. Design, synthesis and biological evaluation of 2-aminopyrimidinones and their 6-aza-analogs as a new class of СК2 inhibitors. J. Enz. Inhib. Med. Chem. 2014, 29, 5, 639­–646.

119.     Ponomarenko, M. V.; Lummer, K.; Fokin, A. A.; Serguchev, Yu. A.; Bassil,B. S.; Röschenthaler, G.-V.  Preparations of SF5- and CF3-substituted arenes utilizing the 7-oxabicyclo­[2.2.1]hept-2-ene synthones. Org. Biomol. Chem. 2013, 11, 8103­–8112.

118.     Kacharov, A. D.; Yemets, S. V.; Nemykin,V. N.; Kacharova, L. M.; Fokin,A. A.; Krasutsky, P. A. Stereoselectivity of A-ring contraction for 3-oxotriterpenoids.  RCS Advances 2013, 3, 19057–19063.

117.     Mishura,A. M.; Sklyarova,A. S.; Sharapa, D. I.; Levandovsky, I. A.; Serafin, M.; Fokin, A. A.; Rodionov, V. N. Stereoselective Preparation of mono- and bis-derivatives of pentacyclo[6.3.0.02,6.03,10.05,9]undecane (D3-trishomocubane). Open. Chem.  2013, 11, 2144–2150.

116.Li, F. H.; Fabbri, J. D.; Yurchenko, R. I.; Mileshkin, A. N.; Hohman, J. N.; Yan, H.; Yuan, H.; Tran, I. C.; Willey, T. M.; Bagge-Hansen, M.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N. A. Covalent attachment of diamondoid phosphonic acid dichlorides to tungsten oxide surfaces. Langmuir 2013, 29, 9790–9797.

115.Zimmermann, T.; Richter, R.; Knecht, A.; Fokin, A. A.; Koso, T. V.; Chernish, L. V.; Gunchenko, P. A.; Schreiner, P. R.; Moller, T.; Rander, T. Exploring covalently bound diamondoid aggregates with valence photoelectron spectroscopy. J. Chem. Phys. 2013, 139, 084310 (6 p).

114.Fokin, A. A.; Butova, E. D.; Barabash, A. V; Huu, N. N.; Tkachenko. B. A.; Fokina, N. A.; Schreiner, P. R. Preparative synthesis of vinyl diamondoids. Synth. Comm. 2013, 43, 1772–1777.

113.Sklyarova, A. S.; Rodionov, V. N.; Parsons, C. G.; Quack, G.; Schreiner, P. R.; Fokin, A. A. Preparation and testing of homocubyl amines as therapeutic NMDA receptor antagonists. Med. Chem. Res. 2013, 22, 360–366.

112.     Clay, W. A.; Maldonado, J. R.;  Pianetta, P.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Melosh, N.; Shen, Z.-X. Photocathode device using diamondoid and cesium bromide films Appl. Phys. Lett. 2012, 101, 241605 (5p).

111.Ishiwata, H.; Acremann, Y.; Scholl, A.; Rotenberg, E.; Hellwig, O.; Dobisz, E.; Doran, A.; Tkachenko, B.A.; Fokin, A.A.; Schreiner, P.R.; Dahl, J.E.P.; Carlson, R.M.K.; Melosh, N.; Shen, Z.-X.; Oldag, H. Diamondoid coating enables disruptive approach for chemical and magnetic imaging with 10 nm spatial resolution. Appl. Phys. Lett. 2012, 101, 163101 (5 p).

110.Fokin, A. A.;  Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Hausmann, H.; Serafin, M.; Dahl J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Stable alkanes containing very long carbon–carbon bonds. J. Am. Chem. Soc. 2012, 134, 1364113650.

109.     Gunchenko, P. A.; Fokin, A. A. Mechanisms of activation of C–H bonds in framework compounds: Theory and experiment. Theoret. Experim. Khim. 2012, 47, 6, 343–360.

108.     Gaidai, A. V.; Volochnyuk, D. M.; Shishkin, O. V.; Fokin, A. A.; Levandovskiy, I. A.; Shubina, T. E. D3-Trishomocubane-4-carboxylic acid as a new chiral building block: Synthesis and absolute configuration. T. E. Synthesis 2012, 44, 810–816.ю

107.Fokina, N. A.; Tkachenko, B. A.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner P. R.  Synthesis of diamondoid carboxylic acid. Synthesis 2012, 44, 259–264.1

106.Fokin, A. A.; Gerbig, D.; Schreiner, P. R. σ/σ- and π/π-Interactions are equally important: multilayered graphanes. J. Am. Chem. Soc. 2011, 133, 20036–20039.

105.Rodionov, V. N.; Sklyarova, A. S.; Shamota, T. V.; Schreiner, P. R.; Fokin, A. A. Selective reductive dimerization of homocubane series oximes. Russ. J. Org. Chem. 2011, 47, 11, 1695−1702.

104.     Schreiner, P. R.; Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Hausmann, H.; Serafin, M.; Schlecht, S.; Dahl J. E. P.; Carlson, R. M. K.; Fokin, A. A. Overcoming  lability of extremely long alkane carbon–carbon bonds through dispersion forces. Nature 2011, 477, 308–311. This paper was featured in Chemical & Engineering News, 89(38), September 19, 2011 [Science & Technology, Concentrates]

103.Novikovskii, A. A.; Gunchenko P. A.; Prikhodchenko P. G.; Serguchev, Yu. A.; Schreiner P. R.; Fokin A.A. Comparative theoretical and experimental analysis of hydrocarbon σ-radical cations. Russ. J. Org. Chem. 2011, 47, 1293–1299.

102.     Shubina, T. E.; Fokin, A. A. Hydrocarbon s-radical cations. WIREs Comput. Mol. Sci. 2011, 1 661679.

101.     Serguchev, Yu. A.; Ponomarenko, M. V.; Lourie, L. F.; Fokin, A. A. Transannular additions of selectfluor and xenon difluoride: regioselectivity and mechanism. J. Phys. Org. Chem. 2011, 24, 407–413.

100.     Butova, E. D.; Barabash, A. V.; Petrova, A. A.; Kleiner, C. M.; Schreiner, P. R.; Fokin. A. A. Stereospecific consecutive epoxide ring expansion with dimethylsulfoxonium methylide, J. Org. Chem. 2010, 75, 18, 6229–6235.

99.    Demchenko, P. Yu.; Gladyshevskii, R. E.; Volkov, S. V.; Kharkova, L. B.; Yanko, O. G.; Fokina, Z. A.; Fokin, A. A. The first nonaselenium ring. Chem. Commun. 2010, 46, 4520–4522.

98.  Lysenko, A. B.; Senchyk, G. A.; Lincke, J.; Lässig, D.; Fokin, A. A.; Butova, E. D.; Schreiner, P. R.; Krautscheid, H.; Domasevitch, K. V. Metal oxide-organic frameworks (MOOFs), a new series of coordination hybrids constructed from molybdenum(VI) oxide and bitopic 1,2,4-triazole linkers. Dalton Trans. 2010, 39, 4223–4231.

97.  Zhuk, T. S.; Bratko, E. Y.; Pashenko, A. E.; Gunchenko, P. A.; Yurchenko, A. G.; Schreiner, P. R.; Fokin, A. A. The “green” synthesis of neuroprotecting drug Memantine. J. Org. Pharm. Chem. 2010, 8, 62–66.

96.  Roth, S.; Leuenberger, D.; Osterwalder, J.; Dahl, J. E.; Carlson, R. M. K.; Tkachenko, B. A. Fokin, A. A.; Schreiner, P. R., Hengsberger, M. Negative-electron-affinity diamondoid monolayers as high-brilliance source for ultrashort electron pulses. Chem. Phys. Lett.  2010, 495, 102–108.

95.  Landt, L.; Bostedt, C.; Wolter, D.; Möller, T.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Kulesza, A.; Bonacic-Koutecky, V. Experimental and theoretical studies of the absorption properties of thiolated diamondoids. J. Chem. Phys. 2010, 132, 144305 (6p).

94.  Landt, L.; Staiger, M.; Wolter, D.; Klünder, K.; Zimmermann, P.; Willey, T. M.; van Buuren, T.; Brehmer, D.; Schreiner, P. R.; Tkachenko, B. A.; Fokin, A. A.; Möller, T.; Bostedt, C. The influence of a single thiol group on the electronic and optical properties of the smallest diamondoid adamantane. J. Chem. Phys. 2010, 132, 0247101(7p).

93.  Levandovskiy, I. A.; Shubina, T. E.; Fokin, A. A. Computational and QSAR study of the alkylnaphthyl ketones adsorption on silver-ion stationary phase.  J. Molec. Mod. 2010, 16, 513–522.

92.  Schreiner, P. R.; Fokin, A. A.; Reisenauer, H. P.;  Tkachenko, B. A.; Vass, E.; Olmstead, M. M.; Bläser, D.; Boese, R.; Dahl, J. E. P.; Carlson, R. M. K. [123]Tetramantane: Parent of a new family of σ-helicenes. J. Am. Chem. Soc. 2009, 131, 11292–11293.

91.  Fokin, A. A.; Gunchenko, P. A.; Novikovsky, A. A.; Shubina, T. E.; Chernyaev, B. V.; Dahl J. E. P.; Carlson, R. M. K.; Yurchenko, A. G.; Schreiner P. R. Photoacetylation of diamondoids: Selectivities and mechanism. Eur. J. Org. Chem. 2009, 5153–5161. This work is featured: Cover picture of the Eur. J. Org. Chem., 2009, issue 30.

90.  Fokin, A. A.; Zhuk, T. S.; Pashenko, A. E.; Dral, P. O.; Gunchenko, P. A.;Dahl, J. E. P.;Carlson, R. M. K.;Koso, T. V.;Serafin, M.; Schreiner, P. R. Oxygen-doped nanodiamonds: Synthesis and functionalizations. Org. Lett. 2009, 11, 3068–3071.

89.  Sklyarova, A. S.; Rodionov, V. N.; Fokin, A. A. A convenient preparative synthesis of pentacyclo[5.3.0.02,5.03,9.04,8]decane (C2-bishomocubane). Russ. J. Org. Chem. 2009, 45, 11, 1644−1647.

88.  Gunchenko, P. A.; Makuhina, A. M.; Novikovsky, A. A.; Yurchenko, A. G.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Structure and transformations of homoadamantane radical cation.  Theoret. and Experim. Khim. 2009, 45, 4, 246–251.

87.  Willey, T. M.; Lee, J. R. I.; Fabbri, J. D.; Wang, D.; Nielsen, M. H.; Randel, J. C.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Dahl, J. E. P.; Carlson, R. M. K.; Terminello, L. J.; Melosh, N. A.; van Buuren, T. Determining orientational structure of diamondoid thiols attached to silver using near-edge X-ray absorption fine structure spectroscopy. J. Elec. Spectr. Rel. Phen. 2009, 172, 69–77.

86.  Schwertfeger, H.; Würtele, C.; Hausmann, H.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R. Selective preparation of diamondoid fluorides. Adv. Synth. Catal. 2009, 351, 1041–1054.

85.  Fokin, A. A.; Schreiner, P. R. Band gap tuning in nanodiamonds: First principle computational studies. Molec. Phys. 2009, 107, 8–12, 823–830.

84.  Fokin, A. A.; Tkachenko, B. A.; Fokina, N.  A.; Hausmann, H.; Serafin, M.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Reactivities of the prism-shaped diamondoids [1(2)3]tetramantane and [12312]hexamantane (cyclohexamantane). Chem. Eur. J. 2009, 15, 3851–3862.

83.  Fokin, A. A.; Merz, A.; Fokina, N. A.; Schwertfeger, H.; Liu, S. L.; Dahl, J. E. P.; Carlson, R. K. M.; Schreiner, P. R.  Synthetic routes to aminotriamantanes, topological analogues of the neuroprotector memantine. Synthesis 2009, 909–912.

82.  Clay, W. A.; Liu, Z.; Yang, W.; Fabbri, J. D.; Dahl, J. E.; Carlson, R. M. K.; Sun, Y.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Pianetta, P. A.; Melosh, N.; Shen Z.-X. Origin of the monochromatic photoemission peak in diamondoid monolayers. Nano Lett. 2009, 9, 57–61.

81.  Willey, T. M.; Fabbri, J. D.; Lee, J. R. I.; Schreiner, P. R.; Fokin, A. A.; Fokina, N. A; Dahl, J. E. P.; Carlson, R. M. K.; Vance, A. L.; Yang, W.; Terminello, L. J.; van Buuren, T.; Melosh, N. A.  Near-edge X-ray absorption fine structure spectroscopy of diamondoid thiol monolayers on gold.  J. Am. Chem. Soc. 2008, 130, 10536–10544.

80.  Chernish, L. V.; Gunchenko, P. A.; Barabash, A. B.; Goreslavets, V. S.; Yurchenko, A. G.; Fokin, A. A. Selective synthesis of 1,1-diadamantane monoderivatives.  Zhurn. Org. Pharm. Khim. 2008, 6, 48–51.

79.  Zhuk, T. S.; Gunchenko, P. A.; Korovai, Ya. Yu.; Schreiner,P. R.; Fokin A. A. Mechanisms of the C–H halogenation of adamantane in the presence of N-hydroxyphthalimide.   Theoret. and Experim. Khim.  2008, 44, 1, 46–51.

78.  Schwertfeger, H; Fokin, A. A.; Schreiner, P. R. Diamonds are a chemist’s best friend: Diamondoid chemistry beyond adamantane.  Angew. Chem. Int. Ed. 2008, 47, 1022–1036.

77.  Fokin, A. A.; Yurchenko, A. G.; Rodionov, V. N.; Gunchenko, P. A.; Yurchenko, R. I.; Reichenberg, A.; Wiesner, J.; Hintz, M.; Jomaa, H.; Schreiner, P.R. Synthesis of the antimalarial drug FR900098 utilizing the nitroso-ene reaction. Org. Lett. 2007, 9, 4379–4382. G

76.  Fokina, N. A.; Tkachenko, B. A.; Merz, A.; Serafin, M.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R. Hydroxy derivatives of diamantane, triamantane, and [121]tetramantane: Selective preparation of bis-apical derivatives. Eur. J. Org. Chem. 2007, 4738–4745.

75.  Butova, E. D.; Fokin, A. A.; Schreiner, P. R. Beyond the Corey reaction: One-Step diolefination of cyclic ketones. J. Org. Chem. 2007, 72, 5689–5696.

74.  Fokin, A. A.; Butova, E. D.; Chernish, L. V.; Fokina, N. A.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Simple preparation of diamondoid 1,3-dienes via oxetane ring opening. Org. Lett. 2007, 9, 2541–2544.0

73.  Yang, W. L.; Fabbri J. D.; Willey, T. M.; Lee, J. R. I.; Dahl, J. E.; Carlson, R. M. K.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Meevasana, W.; Mannella, N.; Tanaka, K.; Zhou, X. J.; van Buuren, T.; Kelly, M. A.; Hussain, Z.; Melosh, N. A.; Shen, Z.-X. Monochromatic electronphotoemission from diamondoid monolayers. Science 2007, 316, 1460–1462.

72.       Wodrich, M. D.; Corminboeuf, C.; Schreiner, P. R.; Fokin, A. A.; Schleyer, P. v. R. How accurate are DFT treatments of organic energies? Org. Lett. 2007, 9, 1851–1854.

71.  Schreiner, P. R.; Fokin, A. A.; Pascal, R. A., Jr.; de Meijere, A. Many density functional theory approaches fail to give reliable large hydrocarbon isomer energy differences. Org. Lett. 2006, 8, 3635–3638.

70.  Fokin, A. A.; Schreiner, P. R.; Fokina, N. A.; Tkachenko, B. A.; Hausmann, H.; Serafin, M. Dahl, J. E. P.; Liu, S.; Carlson, R. M. K.  Functionalized nanodiamonds Part 4: Reactivity of [1(2,3)4]pentamantane (Td-Pentamantane): A nanoscale model of diamond J. Org. Chem. 2006, 71, 8532–8540.

69.   Ponomarenko, M. V.; Serguchev Y. A.; Ponomarenko, B. V.; Röschenthaler, G.-V.; Fokin, A. A. Experimental and theoretical studies on the transannular cyclizations of 3,7-dimethylenebicyclo[3.3.1]nonane with polyfluoroalkyl radicals.  J. Fluor. Chem, 2006, 127, 842–849.

68.  Schreiner, P. R.; Fokina, N. A.; Tkachenko, B. A.; Hausmann, H.; Serafin, M.; Dahl, J. E. P.; Liu, S.; Carlson, R. M. K.; Fokin, A. A. Functionalized Nanodiamonds Part 2: Triamantane and [121]Tetramantane. J. Org. Chem. 2006, 71, 18, 6709–6720. This work is featured: Cover picture of the J. Org. Chem., 2006, issue 18.

67.  Tkachenko, B. A.; Fokina, N. A.; Chernish, L. V.; Dahl, J. E. P.; Liu, S.; Carlson, M. K.; Fokin, A. A.; Schreiner, P. R. Functionalized Nanodiamonds Part 3: Thiolation of tertiary/bridgehead alcohols. Org. Lett. 2006, 8, 1767–1770.

66.  Fokin, A. A.; Schreiner, P. R.; Berger, R.; Robinson, G. H.; Wei, P.; Campana, C. F. Pseudotetrahedral polyhalocubanes: Synthesis, structures, and parity violating energy differences. J. Am. Chem. Soc. 2006, 128, 5332–5333. This work is featured: Nature, 2006, 44, 4, 5.

65.  Fokin, A. A.; Tkachenko, B. A.; Gunchenko, P. A. Gusev, D. V. Schreiner, P. R. Functionalized Nanodiamonds Part I. An experimental assessment of diamantane and computational predictions for higher diamondoids. Chem. Eur. J. 2005, 11, 7091–7101.

64.  de Meijere, A.; Lee, C.-H.; Kuznetsov M. A.; Gusev, D. V.; Kozhushkov, S. I.; Fokin, A. A.; Schreiner, P. R. Preparation and reactivity of [D3d]-octahedrane: The most stable (CH)12 hydrocarbon. Chem. Eur. J. 2005, 11, 6175–6184.

63.  Rodionov, V. N.; Chernyaev, B. V.; Levandovskii, I. A.; Shubina, T. E.; Fokin, A. A..  Quantum-chemical interpretation of the reorientation of dialkyl-cis-9,10-dihydroanthracene-9,10-endofumarates on a silver-containing stationary phase.  Theoret. and Experim. Khim. 2005, 41, 1, 1–6.

62.  Rodionov, V. M.; Chernyaev, B. V.; Levandovs'kii, I. A.; Shubina, T. E.; Fokin, A. A.; Yurchenko, O. G.  Experimental and quantum-chemical study of the thermodynamics of complexation of methylbenzenes with silver(I) ion.    Naukovi Visti - Natsional'nii Tekhnichnii Universitet Ukraini "Kiivs'kii Politekhnichnii Institut"  2005, 1, 107–115.

61.  Fokin, A. A.; Tkachenko, B. A.; Gunchenko, P. A.; Schreiner, P. R. The protonation of cubane revisited. Angew. Chem. Int. Ed. 2005, 44, 146–149.

60.  Schreiner, P. R.; Fokin, A. A.; Kotke, M.; Weil, T. Noncovalent organocatalysis.  Ann. Pol. Chem. Soc. 2004, 3, part 1, 21–24.

59.  Schreiner, P. R.; Fokin, A. A. Selective alkane C–H-bond functionalizations utilizing oxidative single-electron transfer and organocatalysis. Chem. Record 2004, 3, 247–257.

58.  Kiriy, N.; Jahne, E.; Adler, H.-J.; Schneider, M.; Kiriy, A.; Gorodyska, G.; Minko, S.; Jehnichen, D.; Simon,|P.; Fokin, A. A.; Stamm, M. One-dimensional aggregation of regioregular polyalkylthiophenes. Nano Letters 2003, 3, 707–712.

57.  Gunchenko, P. A.; Vigovskaya, T. S.; Fokin, A. A.; Yurchenko, A. G. A New method for building of [3.3.3]propellan skeleton.  Ukr. Khim. Zhurn. 2003, 69, 10, 113–115.

56.  Fokin, A. A.; Schreiner, P. R. Metal-free, selective alkane functionalizations.  Adv. Chem. Cat. 2003, 345, 1035–1052.

55.  de Meijere, A.; Kozhushkov, S. I.; Fokin, A. A.; Emme, I.; Redlich, S.; Schreiner, P. R. New structurally interesting cyclopropane derivatives. A world of wonders and surprises. Pure Appl. Chem. 2003, 75, 549–562.

54.  Fokin, A. A.; Schreiner, P. R.; Kozhushkov, S. I.; Sattelmeyer, K. W.; Schaefer, H. F.; de Meijere, A. Delocalizations in s-radical cations: The Intriguing structures of ionized [n]rotanes.  Org. Lett. 2003, 5, 697–700.

53.  Tkachenko, B. A.; Shubina, T. E.; Gusev, D. V.; Gunchenko, P. A.; Yurchenko, A. G.; Schreiner, P. R.; Fokin, A. A. Mechanisms of C–H Activation of Alkanes by Chromium-oxo Reagents.  Theoret. and Experim. Khim. 2003, 39, 2, 90–95.

52.   Krasutsky, P. A.; Kolomitsyn, I. V.; Botov, E. M.; Carlson, R. M.; Semenova, I. G.; Fokin, A. A. Heterolytic decarboxylation involving acyltrifluoroacetyl peroxide intermediates. Tetrahedron Lett. 2002, 43, 8687–8691.

51.  Schreiner, P. R.; Fokin, A. A.; Lauenstein, O.;  Okamoto, Y.; Wakita, T.; Rinderspacher, C; Robinson, G. H.; Vohs, J. K.; Campana.; C. F. Pseudotetrahedral polyhaloadamantanes as chirality probes: Synthesis, separation, and absolute configuration.  J. Am. Chem. Soc. 2002, 124, 13348–13349.

50.  Fokin, A. A.; Tkachenko, B. A.; Shubina, T. E.; Gunchenko, P. A.; Gusev, D. V.; Vohs, J. K.; Robinson, R. H.; Yurchenko, A. G.; Schreiner, P. R. The protoadamantane radical cation.  Eur. J. Org. Chem. 2002, 3844–3849.

49.  Shubina, T. E.; Gunchenko, P. A.; Vigovskaya, T. S.; Schreiner, P. R.; Yurchenko, A. G.; Fokin, A. A.  [3.3.2]- and [3.3.3]propellanes in reactions with oxidizing electrophiles. Teoret. i Experim. Khimiya, 2002, 38, 4, 226–231.

46.  Kiriy, A. V.; Yurchenko, A. G.; Fokin, A. A. The new [2,3]-sigmatropic rearrangement of allylsulfinyl carbanions. Russ. J. Org. Chem. 2002, 38, 3, 471–472.

48.  Fokin, A. A.; Shubina, T. E.; Gunchenko, P. A.; Isaev, S. D.; Yurchenko, A. G.; Schreiner, P. R. H-Coupled electron transfer in alkane C–H activations with halogen electrophiles. J. Am. Chem. Soc. 2002, 124, 10718–10727.

47.  Fokin, A. A.; Schreiner, P. R. Selective alkane transformations via radicals and radical cations: Insights into the activation step from experiment and theory. Chem. Rev. 2002, 102, 1551–1593.

45.  Shubina, T. E.; Gunchenko. P. A.; Yurchenko, A. G.; Schreiner, P. R.; Butova, E. D.; Fokin, A. A. Structure and transformations of 1-alkyladamantane radical cations.  Teoret. i Experim. Khimiya 2002, 38, 1, 8–13.

44.  Schreiner, P. R.; Lauenstein, O.; Butova, E. D.; Gunchenko, P. V.; Kolomitsin, I. V.; Wittkopp, A.; Feder, G.; Fokin, A. A. Selective radical reactions in multiphase systems: Phase-transfer halogenations of alkanes. Chem. Eur. J. 2001, 7, 23, 4996–5003.

43.  Fokin, A. A.; Tkachenko, B. A.; Korshunov, O. I.; Gunchenko, P. A.; Schreiner, P. R. Molecule-induced alkane homolysis with dioxiranes. J. Am. Chem. Soc. 2001, 123, 11248–11252.

42.  Prall, M.; Wittkopp, A.; Fokin, A. A.; Schreiner, P. R.  Substituent effects on the Bergman Cyclization of (Z)-1,5-hexadiyne-3-enes: A systematic computational study. J. Comp. Chem. 2001, 22, 13, 1605–1614.

41.  Fornarini, S.; Crestone, E.; Fokin, A. A. The protonation of gaseous cyclopropane. Chem. Eur. J. 2001, 7, 2916–2921.

40.  Schreiner, P. R.; Gunchenko, P. A.; Wittkopp, A.; Yaroshinsky, A. I.; Peleshanko, S. A.; Fokin, A. A.  The rearrangement of the cubane radical cation in solution. Chem. Eur. J. 2001, 7, 2739–2744.

39.  Krasutsky, P. A.; Kolomitsyn, I. V.;  Kiprof, P.;  Carlson, R. M.;  Sydorenko, N. A.; Fokin, A. A.  A Consecutive double-Criegee rearrangement using TFPAA: Stepwise conversion of homoadamantane to oxahomoadamantanes.  J. Org. Chem. 2001, 66, 1701–1707.

38.  Fokin, A. A.; Lauenstein, O.; Gunchenko, P. A.; Schreiner, P. R.  Halogenation of cubane under phase-transfer conditions: Single and double C–H-bond substitution with conservation of the cage Structure.  J. Am. Chem. Soc.  2001, 123, 1842–1847.

37.  Fokin, A. A.; Peleshanko, S. A.; Gunchenko, P. A.; Gusev, D. V.; Schreiner, P. R. Hydrocarbon activations with cerium (IV) ammonium nitrate: Free radical versus oxidative pathways. Eur. J. Org. Chem. 2000, 3357–3362.

36.  Lauenstein, O.; Fokin, A. A.; Schreiner, P. R. A combined experimental and computational study of the H/D kinetic isotope effects for bromination and iodination of aliphatic hydrocarbons under phase-transfer conditions. Org. Lett.  2000, 2201–2204.

35.  Fokin,A. A.;Schreiner,P. R.; Gunchenko, P. A.; Peleshanko, S. A.; Shubina,T. E.; Isaev, S. D.; Tarasenko, P. V.; Kulik, N. I.; Schiebel, H.-M.; YurchenkoA. G. Oxidative single electron transfer activation of s-bonds in aliphatic halogenation reactions. J. Am. Chem. Soc. 2000, 122, 7317–7326.

34.  Fokin, A. A.; Kushko, A. O.; Kirij, A. V.; Yurchenko, A. G.; Schleyer, P. v. R. Direct transformations of ketones to g-unsaturated thiols via [2,3]-sigmatropic rearrangement of allyl sulfinyl carbanions: Combined experimental and theoretical study. J. Org. Chem. 2000, 65, 2984–2995.

33.  Kolomitsin, I. V.; Krasutsky, P. A.; Sidorenko, N. V.; Yurchenko, A. G.; Fokin, A. A.  Oxidative fragmentation of tetrahydrocyclopentadiene structure. Russ. J. Org. Chem. 2000,  36, 456–457.

32.  Krasutsky, P. A.; Kolomitsin, I. V.; Kiprof, P.; Carlson, R. M.; Fokin, A. A. Observation of a stable carbocation in a consecutive Criegee rearrangement with trifluoroperacetic acid. J. Org. Chem. 2000, 65, 3926–3933.

31.  Fokin, A.A.; Kiran, B.; Bremer, M.; Yang, X.; Jiao, H.; Schleyer, P. v. R.  Which electron count rules are needed for four-centered tree-dimensional aromaticity? Chem. Eur. J.; 2000, 6, 1615–1628.

30.  Schreiner, P. R.; Lauenstein, O.; Butova, E. D.; Fokin, A. A. The first efficient iodination of unactivated, aliphatic hydrocarbons. Angew. Chem. 1999, 111 2956–2958. Angew. Chem. Int. Ed. Engl. 1999, 38, 2786–2788. This work is featured: cover picture of the Angewandte Chemie, 1999, issue 18. Chemical and Engineering News 1999 September, 20, 44. Sueddeutsche Zeitung 1999 55, October, 12, p. V2/12.

29.  Fokin, A. A.; Gunchenko, P. A.; Peleshanko, S. A.; Schleyer, P. v. R.; Schreiner, P. R. Common radical cation intermediates in cage hydrocarbon activations.  Eur. J. Org. Chem. 1999, 855–860.

28.  Kushko, A. O.; Yurchenko, A. G.; Kirij, A. V.; Likhotvorik, I. R.; Fokin, A. A.  The novel one-step method of homoallylic tiols synthesis from ketons. Russ. J. Org. Chem. 1998, 34, 776–777.

27.  Fokin, A. A.; Schreiner, P. R.; Schleyer, P. v. R.; Gunchenko, P. A. Electrophilic and oxidative activation of the central C–C Bond in [3.3.n]Propellanes: A theoretical study. J. Org. Chem. 1998,No19, 6494–6502.

26.  Fokin, A. A.; Jiao, H.; Schleyer, P. v. R. From Dodecaheptapentaene to the “[n]Trannulenes”. A new In-plane aromatic family.  J. Am. Chem. Soc. 1998, 120, 9364–9365.

25.  Schreiner, P. R.; Lauenstein, O.; Kolomitsin, I. V.; Fokin, A. A.  Selective C–H activation of aliphatic hydrocarbon under phase-transfer conditions.  Angew. Chem.; Int. Ed. 1998, 37, 1895–1897. This paper was featured in Nachr. Chem. Tech. Lab. 1998 7/8, 706. Chemical and Engineering News 1998 July, 13, 55.

24.  Fokin, A. A.; Gunchenko, P. A.; Tkachenko, B. A.; Butova, E. D.; Yurchenko, A. G.  Backside activation of s-bonds with Cr(VI)-reagents.  Tetrahedron Lett. 1997, 38, 639–642.

23.  Fokin, A. A.; Gunchenko, P. A.; Kulik, N. I.; Iksanova, S. V.; Krasutsky, P. A.; Gogoman, I. V.; Yurchenko, A. G.  NO2+-containing reagents in the electrophilic and oxidative addition to propellanic C–C bond.  Tetrahedron 1996, 52, 5857–5866.

22.  Fokin, A. A.; Gunchenko, P. A.; Krasutsky, P. A.; Yaroshinsky, A. I.; Yurchenko, A. G. Oxidation of tetracyclo[4.3.1.1.4,801,4]undecane (1,4-cyclohomoadamantane). Russ. J. Org. Chem. 1995, 31, 796–797.

21.  Fokin, A. A.; Gunchenko, P. A.; Krasutsky, P. A.; Yaroshinsky, A. I.; Yurchenko, A. G. Oxidative addition to 3,6-dehydrohomoadamantane.  Tetrahedron Lett. 1995, 36, 4479–4482.

20.  Fokin, A. A.; Gagaeva, E. A.; Krasutsky, P. A.; Yurchenko, A. G. Stereoselective epoxidation of 4,7,7-trimethyl-3-oxabicyclo[3.3.1]hept-4-en-2-one. Russ. J. Org. Chem. 1994, 30, 940–941.

19.  Fokin, A. A.; Butova, E. D.; Kolomitsin, I. V.; Gagaeva, E. A.; Kornilov, A. M.; Sorochinsky A. E. Functional derivatives of 2-carene in cyclopropane-containing pyrethroides synthesis. Russ. J. Org. Chem. 1994, 30, 669–679.

18.  Fokin, A. A.; Butova, E. D.; Gulevitch, A. V.; Yurchenko, A. G.; Krasutsky, P. A.  Novel oxidative transformations in norpinonic acid synthesis. Russ. J. Org. Chem. 1993, 29, 1075–1076.

17.  Lichotvorik, I. R.; Litvin, A. L.; Shimko, R. I.; Fokin, A. A. The insertion of dichlorocarbene into tricyclo[5.2.1.02,5]decane structure. Vest. Kiev Polytech. Inst. 1992, 29, 3.

16.  Fokin, A. A.; Krasutsky, P. A.; Gulevich, A.V.; Yurchenko, A. G.  Oxidation of 3,7,7-trimethyl-3,4-dihydroxybicyclo[4.1.0]heptane by molecular oxygen. Russ. J. Org. Chem. 1992, 28, 1098–1099.

15.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structures of 1R-cis-polyhalogenchrysanthemic acids. Russ. J. Org. Chem. 1992, 28, 67–75.

14.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G.  Key synthones of pyrethrinoides based on 3-carene.  Ukr. Khim. Zhurnal 1992, 58, 1130–1135.

13.  Fokin, A. A.; Fedorenko, T. V.; Yurchenko, A. G. Enantioselective synthesis of chrysanthemic acid and derivatives. Ukr. Khim. Zhurnal 1992, 58, 1120–1126.

12.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structure of the stereoisomeric monochlorochrysanthemic acids. Russ. J. Org. Chem. 1991, 27, 1279–1283.

11.  Fokin, A. A.; Krasutsky, P. A.; Baula, O. P.; Yurchenko, A. G.  Functionalization of 4,7,7-trimethyl-3-oxabicyclo[3.31]hept-4-en-2-one with dichlorocarbene. Russ. J. Org. Chem. 1991, 27, 1363.

10.  Krasutsky, P. A.; Fokin, A. A.; Rodionov, V. N.; Kulik, N. I.; Ambrosienko, N. V.; Yurchenko, A. G.  On the mechanisms of transannular acidic cyclization of 3,7-dimethylenobicyclo[3.3.1]nonane and derivatives. Russ. J. Org. Chem. 1991, 27, 992–999.

9.      Krasutsky, P. A.; Fokin, A. A.; Butova, E. D.; Yurchenko, A. G. Stereoselective synthesis of (–)-pirocine and 1R-E-chrysanthemic acid from 2-pinene. Vest. Kiev. Polytech. Inst. 1991, 28, 40–44.

8.      Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G. The structures of carbenilation products of 2-pinene and 3-carene with carboethoxycarbene. Ukr. Khim. Zhurnal 1989, 55,  842–845.

7.      Krasutsky, P. A.; Fokin, A. A.; Maleev, A. V.; Kurkutova, E. N.; Struchkov, Y. T.; Yurchenko, A. G. The structure of adducts of allenes of bicyclo[3.3.1]nonane series with dihalocarbenes. Russ. J. Org. Chem. 1990, 26, 1016–1024.

6.      Krasutsky, P. A.; Fokin, A. A.; Skoba, E. D.; Yurchenko, A. G. the synthesis and protic cyclization of 3-vinylidenobicyclo[3.3.1]nonane-7-one. Russ. J. Org. Chem. 1986, 22, 460–461.

5.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and protic cyclization of 3-vinylideno-7-propadienilidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1986, 22, 459–460.

4.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and reactivity of 3-methylene-7-vinylidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1985, 21, 2522–2626.

3.      Krasutsky, P. A.; Fokin, A. A.; Kulik, N. I.; Yurchenko, A. G. The reactivity of 3,7-divinylidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1985, 21, 2518–2522.

2.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G.; Chekmenyova, L. A. The synthesis of 3,7-divinylidenbicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1984, 20, 1807–1808.

1.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G.; Jones, M. Jr.; Antipin, M. Y.; Struchkov, Y. T. The structure of carbenylation products of 3-methylenebicyclo[3.3.1]nonane. Teoret. i Experim. Khimiya 1984, 20, 427–433.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

159. Becker, J.; Zhyhadlo, Y. Y.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Ferster, M.; Holthausen, M. C.; Specht, P.; Schindler, S.  Aerobic aliphatic hydroxylation reactions by copper complexes: A simple clipandcleave concept. Chem. Eur. J.2018, 24, https://doi.org/10.1002/chem.201802607

158.Gebbie, M. A.; Ishiwata, H.;  McQuade P.J.; Petrak, V.: Taylor, A.; Freiwald, C.; Dahl, J. E.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Nesladek, M.; Melosh, N. A. Experimental measurement of the diamond nucleation landscape reveals classical and nonclassical features. PNAS, 2018, 115, 33, 8284–8289.

157. Moncea, O.; Poinsot, D.; Fokin, A. A.; Schreiner, P. R.; Hierso, J. C. Palladium-catalyzed C2-H arylation of unprotected (N-H)-indoles “On water” using primary diamantyl phosphine oxides as a class of primary phosphine oxide ligands. ChemCatChem, 2018, 10, 2915 – 2922.

155.Hoc, N. T.  Fokin, A. A; Rodionov, V. N. Towards 3-(2-adamantylidene)diamantane derivatives through the McMurry cross coupling reaction. Org. Commun. 2018, 11, 2x, 75-79.

156. Hoc, N. T.  Fokin, A. A; Rodionov, V. N. Synthesis of 10-methoxydiamantan-3-one. MOLBANK. 2018, 2, UNSP M990. DOI: 10.3390/M990

154.Yan, H.;Narasimha, K. T.; Denlinger, J.;Li, F. H.;Mo, S.-K.;Nathan Hohman, J.;  Dahl, J. E. P.; ,Carlson, R. M. K.;Tkachenko, B. A.;Fokin, A. A.; Schreiner, P. R.; Hussain, Z.; Shen, Z.-X.; ,Melosh, N. A.Monochromatic photocathodes from graphene-stabilized diamondoids. Nano Lett., 2018, 18, 1099–1103.

153.Yan, H.; Yang, F.; Pan, D.; Lin, Y.; Hohman, J. N.; Solis-Ibarra, D.; Li, F. H.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Galli, G.; Mao, W. L.; Shen Z.-X.; Melosh, N. M. Sterically controlled mechanochemistry under hydrostatic pressure. Nature 2018, 554, 505–510.

152.Gunawan, M. A.; Moncea, O.; Poinsot, D.; Keskes, M.; Domenichini, B.; Heintz, O.; Chassagnon, R.; Herbst, F.; Carlson, R. M. K.; Dahl, J. E. P.; Fokin, A. A.; Schreiner, P. R.; Hierso,  J.-C. Nanodiamond-Palladium Core–Shell Organohybrid Synthesis: A Mild Vapor-Phase Procedure Enabling Nanolayering Metal onto Functionalized sp3-Carbon. Adv. Funct. Mater. 2018, 1705786 (15 p).

151.Gunchenko, P. A.; Li,J.; Liu, B.; Chen, H.; Pashenko, A. P.;Bakhonsky, V. V.; Zhuk. T. S.; Fokin, A. A. Aerobic oxidations with N-hydroxyphthalimide in trifluoroacetic acid. Molec. Cat. 2018, 446, 72-79.

150.Zhyhadlo, Y. Y.; Gaidai, A. V.; Sharapa, D. I.; Mitlenko, A. G.; Shishkin, O. V.; Shishkina, S. V.; Levandovskiy, I. A.; Fokin, A. A. Functionalised Cookson's diketones in chlorosulfonic acid: Towards polysubstituted D3-trishomocubanes. J. Chem. Res. 2017, 41, 12, 677-733.

149.Tyborski, C.; Gillen, R.; Fokin, A. A.; Koso, T. V.; Fokina, N. A.; Hausmann, H.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. Electronic and Vibrational Properties of Diamondoid Oligomers. J. Phys. Chem. 2017, 121, 48, 27082–27088

148.     Fokin, A. A.: Zhuk, T. S.; Blomeyer, S.; Peŕez, C.;  Chernish, L.V.; Pashenko, A. E.; Antony, J.; Vishnevskiy, Y. V.;  Berger, R. J. F.; Grimme, S.; Logemann, C.; Schnell, M.; Mitzel N. W.; Schreiner P. R. Intramolecular London dispersion interaction effects on gas-phase and solid-state structures of diamondoid dimers. J. Amer. Chem. Soc. 2017, 139, 16696-16707.

147.     Tyborski, C.; Meinke, R.; Gillen, R.; Bischoff, T.; Knecht, A.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N. Schreiner, P. R.; Moller, T.; Rander, T.; Thomsen, C.; Maultzsch, J. From isolated diamondoids to a van-der-Waals crystal: A theoretical and experimental analysis of a trishomocubane and a diamantane dimer in the gas and solid phase. J. Chem. Phys. 2017, 147, 4, 044303 (6 p.)

146.     Fokin, A. A.; Pashenko, A. E.; Bakhonsky, V. V.; Zhuk. T. S.; Chernish. L. V.; Gunchenko, P. A.; Kushko, A. O.; Becker, J.; Wende, R. C.; Schreiner. P. R. Chiral building blocks based on 1,2-disubstituted diamantanes. Synthesis, 2017. 49, 20032008.

145.     Yan, H.; Hohman, J. N.; Li, F. H.; Jia, C.; Solis-Ibarra, D.; Wu, B.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Vailionis, A.; Kim, T. R.; Devereaux, T. P.; Shen, Z.-X.; Melosh. N. A. Hybrid metal–organic chalcogenide nanowires with electrically conductive inorganic core through diamondoid-directed assembly. Nat. Mater. 2017, 16, 349–355.

144.  Hoc, N. T.;Kushko, A. O.;Fokin, A. A.;Rodionov, V. N. Functional derivatives of diamantanone. Russ. J. Org. Chem. 2016, 52, 8, 1209–1211.

143.Moncea O.; Gunawan, M. A.; Poinsot,D.; Cattey. H.;Becker,J.;Yurchenko,R. I.; Butova,E. D.; Hausmann,H.; Šekutor,M.; Fokin, A. A.; Hierso,J.-C.; Schreiner, P. R. Defying stereotypes with nanodiamonds: Stable primary diamondoid phosphines,  J. Org. Chem. 2016, 81, 8759−8769.

142.     Tverdiy, D. O. Chekanov, M. O.; Savitskiy, P. V.; Syniugin, A. R.; Yarmoliuk, S. M. Fokin, A. A. Efficient preparation of imidazo[1,5-a]pyridine-1-carboxylic acids. Synthesis 2016, 48, A–I.

141.     Ponomarenko, M. V.; Grabowsky,S.; Pal,R.; Röschenthaler, G.-V., Fokin, A. A. SF5-Enolates in Ti(IV)-mediated aldol reactions. J. Org. Chem. 2016, 81, 6783−6791.

140.     Karthik, T. N.; Ge,C.; Fabbri,J. D.; Clay,W.; Tkachenko, B. A.; Fokin, A.A.; Schreiner, P. R.; Dahl, J. E.; Carlson, R. M. K.; Shen, Z. X.; Melosh, N. A. Ultra-low effective work function surfaces using diamondoid monolayers. Nature Nanotech. 2016, 11, 267–273.

139.     Zhang, J. L.; Ishiwata, H.; Babinec, T. M.; Radulaski, M.; Müller, K.; Lagoudakis, K. G.; Dory, C.; Dahl, J.; Edgington, R.; Soulière, V.; Ferro, G.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N.; Vuckovic, J. Hybrid group IV nanophotonic structures incorporating diamond silicon-vacancy color centers. Nano Lett. 2016, 16, 212−217.

138.Syniugin, A. R.; Chekanov, M. O.; Savitskiy, P. V.; Pashenko, A. E.; Zhuk, T. S.; Yarmoluk, S. M.; Fokin, A A. New method for the synthesis of pyrrolo[2,3-b]dihydroquinolines. Tetrahedron Lett.  2016, 57, 213–215.

137.Valentin, L.; Henss, A.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Becker, S.; Würtele, C.; Schindler, S. Transition metal complexes with cage-opened diamondoid tetracyclo[7.3.1.14,12.02,7]tetradeca-6.11-diene. J. Coor. Chem. 2015, 68, 3295–3301.

136.Lourie, L. F.; Serguchev, Yu. A.; Bentya, A. V.; Ponomarenko, M. V.; Rusanov, E. B.; Vovk, M. V.; Fokin, A. A.; Ignat’ev, N. V. Metal free electrophilic fluoro-cyclization of unsaturated N-hydroxy- and N-acetoxyamides with N–F reagents. J. Fluor. Chem. 2015, 179, 42–47.

135.Bremer, M.; Untenecker, H.; Gunchenko, P. A.; Fokin, A. A.; Schreiner P. R.  Inverted carbon geometries: Challenges to experiment and theory. J. Org. Chem. 2015, 80, 6520−6524.

134.     Zhuk, T. S.; Koso, T.; Pashenko, A. E.; Hoc, N. T.; Rodionov, V. N.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Toward an understanding of diamond sp2-defects with unsaturated diamondoid oligomer model. J. Am. Chem. Soc. 2015, 137, 6577−6586.

133.     Gunawan, M. A.; Poinsot, D.; Domenichini, B.; Dirand, C.; Chevalier, S.; Fokin, A. A.; Schreiner, P. R.; Hierso, J.-P. The functionalization of nanodiamonds (diamondoids) as a key parameter of their easily controlled self-assembly in micro- and nanocrystals from the vapor phase. Nanoscale, 2015, 7, 1956–1962.

132.     Barabash, A. V.; Didukh, N. A.; Kibal’nyi, N. A.; Butova, E. D.; Schreiner, P. R.;Fokin, A. A. Unusual aerobic oxidation of sterically hindered 1-diamanty methyl ketone. Russ. J. Org. Chem. 2014, 50, 1690–1691.

131.       Gunchenko, P. A.; Novikovskii, A. A.; Byk, M. V.; Fokin, A. A.  Structure and transformations of diamantane radical cation: Theory and experiment. Russ. J. Org. Chem. 2014, 50, 1749–1754.

130.Mishura, A. M.; Sklyarova, A. S.; Shamota, T. V.: Rodionov, V. N.; Fokin, A. A.  Preparative synthesis of pentacyclo[6.3.0.02,6.03,10.05,9]undecan-4-one (D3-Trishomocubanone). Russ. J. Org. Chem. 2014, 50, 1542–1544.

129.Barabash, A. V.; Butova, E. D.; Kanyuk, I. M.; Schreiner, P. R.; Fokin, A. A. Beyond the Corey reaction II: Dimethylenation of sterically congested ketones J. Org. Chem. 2014, 79, 10669−10673. ACS Editor’s Choice, 01.10.2014.

128.Randel, J. C.; Niestemski, F. C.; Botello-Mendez, A. R.; Mar, W.; Ndabashimiye, G.; Melinte, S.; Dahl, J. E. P.; Carlson R. M. K.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Charlier, J.-C.; Manoharan, H. C. Unconventional molecule-resolved current rectification in diamondoid fullerene hybrids. Nature Comm. 2014, 5, 4877 (6 p).

127.Tchernobaev, I. I.; Serguchev, Yu. A.; Fokin, A. A. Mechanism and selectivities of the chlorination of toluene in the presence of catalytical composition antimony pentachloride – benzodithio crown ether. Ukr. Krim. Zhurn. 2014, 50, 45–49.

126.Ponomarenko, M. V.; Serguchev, Yu. A.; Hirschberg, M. E.; Röschenthaler, G.-V.; Fokin, A. A. Elemental F2 with transannular dienes: Regioselectivities and mechanisms. Chem. Eur. J. 2014, 20, 10383–10391.

125.Fokin, A.A.; Yurchenko, R. I.; Tkachenko,B.A.; Fokina,N. A.; Gunawan,M. A.; Poinsot,D.; Dahl, J. E. P.; Carlson,R. M. K.; Serafin,M.; Cattey,H.; Hierso,J.-C.; Schreiner, P. R. Selective preparation of diamondoid phosphonates. J. Org. Chem. 2014, 79, 5369–5373.

124.Fokin, A. A.; Zhuk, T. S.; Pashenko, A. E.; Osipov, V. V.; Gunchenko,P. A.; Serafin, M.; Schreiner, P. R. Functionalization of homodiamantane: Oxygen insertion reactions without rearrangement with dimethyldioxirane. J. Org. Chem. 2014, 79, 1861–1866.

123.Meinke, R.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. UV resonance Raman analysis of trishomocubane and diamondoid dimers. J. Chem. Phys. 2014, 140, 034309 (5p).

122.Kahl, P.; Tkachenko, B. A.; Novikovsky, A. A.; Backer, J.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.  Efficient peparation of aically substituted damondoid drivatives, Synthesis 2014, 46, 787–798.

121.Gunawan, M. A.; Hierso, J.-C.; Poinsot, D.; Fokin, A. A.; Fokina, N. A.; Tkachenko, B. A.;Schreiner, P. R. Diamondoids: Functionalization and subsequent applications of perfectly defined molecular cage hydrocarbons. New J. Chem. 2014, 38, 28–41.

120.     Chekanov, M. O.; Ostrynska, O. V.; Tarnavskyi, S. S.; Synyugin, A. R.; Briukhovetska, N. V.; Bdzhola, V. G.; Pashenko, A. E.; Fokin A. A.; Yarmoluk, S. M. Design, synthesis and biological evaluation of 2-aminopyrimidinones and their 6-aza-analogs as a new class of СК2 inhibitors. J. Enz. Inhib. Med. Chem. 2014, 29, 5, 639­–646.

119.     Ponomarenko, M. V.; Lummer, K.; Fokin, A. A.; Serguchev, Yu. A.; Bassil,B. S.; Röschenthaler, G.-V.  Preparations of SF5- and CF3-substituted arenes utilizing the 7-oxabicyclo­[2.2.1]hept-2-ene synthones. Org. Biomol. Chem. 2013, 11, 8103­–8112.

118.     Kacharov, A. D.; Yemets, S. V.; Nemykin,V. N.; Kacharova, L. M.; Fokin,A. A.; Krasutsky, P. A. Stereoselectivity of A-ring contraction for 3-oxotriterpenoids.  RCS Advances 2013, 3, 19057–19063.

117.     Mishura,A. M.; Sklyarova,A. S.; Sharapa, D. I.; Levandovsky, I. A.; Serafin, M.; Fokin, A. A.; Rodionov, V. N. Stereoselective Preparation of mono- and bis-derivatives of pentacyclo[6.3.0.02,6.03,10.05,9]undecane (D3-trishomocubane). Open. Chem.  2013, 11, 2144–2150.

116.Li, F. H.; Fabbri, J. D.; Yurchenko, R. I.; Mileshkin, A. N.; Hohman, J. N.; Yan, H.; Yuan, H.; Tran, I. C.; Willey, T. M.; Bagge-Hansen, M.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N. A. Covalent attachment of diamondoid phosphonic acid dichlorides to tungsten oxide surfaces. Langmuir 2013, 29, 9790–9797.

115.Zimmermann, T.; Richter, R.; Knecht, A.; Fokin, A. A.; Koso, T. V.; Chernish, L. V.; Gunchenko, P. A.; Schreiner, P. R.; Moller, T.; Rander, T. Exploring covalently bound diamondoid aggregates with valence photoelectron spectroscopy. J. Chem. Phys. 2013, 139, 084310 (6 p).

114.Fokin, A. A.; Butova, E. D.; Barabash, A. V; Huu, N. N.; Tkachenko. B. A.; Fokina, N. A.; Schreiner, P. R. Preparative synthesis of vinyl diamondoids. Synth. Comm. 2013, 43, 1772–1777.

113.Sklyarova, A. S.; Rodionov, V. N.; Parsons, C. G.; Quack, G.; Schreiner, P. R.; Fokin, A. A. Preparation and testing of homocubyl amines as therapeutic NMDA receptor antagonists. Med. Chem. Res. 2013, 22, 360–366.

112.     Clay, W. A.; Maldonado, J. R.;  Pianetta, P.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Melosh, N.; Shen, Z.-X. Photocathode device using diamondoid and cesium bromide films Appl. Phys. Lett. 2012, 101, 241605 (5p).

111.Ishiwata, H.; Acremann, Y.; Scholl, A.; Rotenberg, E.; Hellwig, O.; Dobisz, E.; Doran, A.; Tkachenko, B.A.; Fokin, A.A.; Schreiner, P.R.; Dahl, J.E.P.; Carlson, R.M.K.; Melosh, N.; Shen, Z.-X.; Oldag, H. Diamondoid coating enables disruptive approach for chemical and magnetic imaging with 10 nm spatial resolution. Appl. Phys. Lett. 2012, 101, 163101 (5 p).

110.Fokin, A. A.;  Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Hausmann, H.; Serafin, M.; Dahl J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Stable alkanes containing very long carbon–carbon bonds. J. Am. Chem. Soc. 2012, 134, 1364113650.

109.     Gunchenko, P. A.; Fokin, A. A. Mechanisms of activation of C–H bonds in framework compounds: Theory and experiment. Theoret. Experim. Khim. 2012, 47, 6, 343–360.

108.     Gaidai, A. V.; Volochnyuk, D. M.; Shishkin, O. V.; Fokin, A. A.; Levandovskiy, I. A.; Shubina, T. E. D3-Trishomocubane-4-carboxylic acid as a new chiral building block: Synthesis and absolute configuration. T. E. Synthesis 2012, 44, 810–816.ю

107.Fokina, N. A.; Tkachenko, B. A.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner P. R.  Synthesis of diamondoid carboxylic acid. Synthesis 2012, 44, 259–264.1

106.Fokin, A. A.; Gerbig, D.; Schreiner, P. R. σ/σ- and π/π-Interactions are equally important: multilayered graphanes. J. Am. Chem. Soc. 2011, 133, 20036–20039.

105.Rodionov, V. N.; Sklyarova, A. S.; Shamota, T. V.; Schreiner, P. R.; Fokin, A. A. Selective reductive dimerization of homocubane series oximes. Russ. J. Org. Chem. 2011, 47, 11, 1695−1702.

104.     Schreiner, P. R.; Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Hausmann, H.; Serafin, M.; Schlecht, S.; Dahl J. E. P.; Carlson, R. M. K.; Fokin, A. A. Overcoming  lability of extremely long alkane carbon–carbon bonds through dispersion forces. Nature 2011, 477, 308–311. This paper was featured in Chemical & Engineering News, 89(38), September 19, 2011 [Science & Technology, Concentrates]

103.Novikovskii, A. A.; Gunchenko P. A.; Prikhodchenko P. G.; Serguchev, Yu. A.; Schreiner P. R.; Fokin A.A. Comparative theoretical and experimental analysis of hydrocarbon σ-radical cations. Russ. J. Org. Chem. 2011, 47, 1293–1299.

102.     Shubina, T. E.; Fokin, A. A. Hydrocarbon s-radical cations. WIREs Comput. Mol. Sci. 2011, 1 661679.

101.     Serguchev, Yu. A.; Ponomarenko, M. V.; Lourie, L. F.; Fokin, A. A. Transannular additions of selectfluor and xenon difluoride: regioselectivity and mechanism. J. Phys. Org. Chem. 2011, 24, 407–413.

100.     Butova, E. D.; Barabash, A. V.; Petrova, A. A.; Kleiner, C. M.; Schreiner, P. R.; Fokin. A. A. Stereospecific consecutive epoxide ring expansion with dimethylsulfoxonium methylide, J. Org. Chem. 2010, 75, 18, 6229–6235.

99.    Demchenko, P. Yu.; Gladyshevskii, R. E.; Volkov, S. V.; Kharkova, L. B.; Yanko, O. G.; Fokina, Z. A.; Fokin, A. A. The first nonaselenium ring. Chem. Commun. 2010, 46, 4520–4522.

98.  Lysenko, A. B.; Senchyk, G. A.; Lincke, J.; Lässig, D.; Fokin, A. A.; Butova, E. D.; Schreiner, P. R.; Krautscheid, H.; Domasevitch, K. V. Metal oxide-organic frameworks (MOOFs), a new series of coordination hybrids constructed from molybdenum(VI) oxide and bitopic 1,2,4-triazole linkers. Dalton Trans. 2010, 39, 4223–4231.

97.  Zhuk, T. S.; Bratko, E. Y.; Pashenko, A. E.; Gunchenko, P. A.; Yurchenko, A. G.; Schreiner, P. R.; Fokin, A. A. The “green” synthesis of neuroprotecting drug Memantine. J. Org. Pharm. Chem. 2010, 8, 62–66.

96.  Roth, S.; Leuenberger, D.; Osterwalder, J.; Dahl, J. E.; Carlson, R. M. K.; Tkachenko, B. A. Fokin, A. A.; Schreiner, P. R., Hengsberger, M. Negative-electron-affinity diamondoid monolayers as high-brilliance source for ultrashort electron pulses. Chem. Phys. Lett.  2010, 495, 102–108.

95.  Landt, L.; Bostedt, C.; Wolter, D.; Möller, T.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Kulesza, A.; Bonacic-Koutecky, V. Experimental and theoretical studies of the absorption properties of thiolated diamondoids. J. Chem. Phys. 2010, 132, 144305 (6p).

94.  Landt, L.; Staiger, M.; Wolter, D.; Klünder, K.; Zimmermann, P.; Willey, T. M.; van Buuren, T.; Brehmer, D.; Schreiner, P. R.; Tkachenko, B. A.; Fokin, A. A.; Möller, T.; Bostedt, C. The influence of a single thiol group on the electronic and optical properties of the smallest diamondoid adamantane. J. Chem. Phys. 2010, 132, 0247101(7p).

93.  Levandovskiy, I. A.; Shubina, T. E.; Fokin, A. A. Computational and QSAR study of the alkylnaphthyl ketones adsorption on silver-ion stationary phase.  J. Molec. Mod. 2010, 16, 513–522.

92.  Schreiner, P. R.; Fokin, A. A.; Reisenauer, H. P.;  Tkachenko, B. A.; Vass, E.; Olmstead, M. M.; Bläser, D.; Boese, R.; Dahl, J. E. P.; Carlson, R. M. K. [123]Tetramantane: Parent of a new family of σ-helicenes. J. Am. Chem. Soc. 2009, 131, 11292–11293.

91.  Fokin, A. A.; Gunchenko, P. A.; Novikovsky, A. A.; Shubina, T. E.; Chernyaev, B. V.; Dahl J. E. P.; Carlson, R. M. K.; Yurchenko, A. G.; Schreiner P. R. Photoacetylation of diamondoids: Selectivities and mechanism. Eur. J. Org. Chem. 2009, 5153–5161. This work is featured: Cover picture of the Eur. J. Org. Chem., 2009, issue 30.

90.  Fokin, A. A.; Zhuk, T. S.; Pashenko, A. E.; Dral, P. O.; Gunchenko, P. A.;Dahl, J. E. P.;Carlson, R. M. K.;Koso, T. V.;Serafin, M.; Schreiner, P. R. Oxygen-doped nanodiamonds: Synthesis and functionalizations. Org. Lett. 2009, 11, 3068–3071.

89.  Sklyarova, A. S.; Rodionov, V. N.; Fokin, A. A. A convenient preparative synthesis of pentacyclo[5.3.0.02,5.03,9.04,8]decane (C2-bishomocubane). Russ. J. Org. Chem. 2009, 45, 11, 1644−1647.

88.  Gunchenko, P. A.; Makuhina, A. M.; Novikovsky, A. A.; Yurchenko, A. G.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Structure and transformations of homoadamantane radical cation.  Theoret. and Experim. Khim. 2009, 45, 4, 246–251.

87.  Willey, T. M.; Lee, J. R. I.; Fabbri, J. D.; Wang, D.; Nielsen, M. H.; Randel, J. C.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Dahl, J. E. P.; Carlson, R. M. K.; Terminello, L. J.; Melosh, N. A.; van Buuren, T. Determining orientational structure of diamondoid thiols attached to silver using near-edge X-ray absorption fine structure spectroscopy. J. Elec. Spectr. Rel. Phen. 2009, 172, 69–77.

86.  Schwertfeger, H.; Würtele, C.; Hausmann, H.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R. Selective preparation of diamondoid fluorides. Adv. Synth. Catal. 2009, 351, 1041–1054.

85.  Fokin, A. A.; Schreiner, P. R. Band gap tuning in nanodiamonds: First principle computational studies. Molec. Phys. 2009, 107, 8–12, 823–830.

84.  Fokin, A. A.; Tkachenko, B. A.; Fokina, N.  A.; Hausmann, H.; Serafin, M.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Reactivities of the prism-shaped diamondoids [1(2)3]tetramantane and [12312]hexamantane (cyclohexamantane). Chem. Eur. J. 2009, 15, 3851–3862.

83.  Fokin, A. A.; Merz, A.; Fokina, N. A.; Schwertfeger, H.; Liu, S. L.; Dahl, J. E. P.; Carlson, R. K. M.; Schreiner, P. R.  Synthetic routes to aminotriamantanes, topological analogues of the neuroprotector memantine. Synthesis 2009, 909–912.

82.  Clay, W. A.; Liu, Z.; Yang, W.; Fabbri, J. D.; Dahl, J. E.; Carlson, R. M. K.; Sun, Y.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Pianetta, P. A.; Melosh, N.; Shen Z.-X. Origin of the monochromatic photoemission peak in diamondoid monolayers. Nano Lett. 2009, 9, 57–61.

81.  Willey, T. M.; Fabbri, J. D.; Lee, J. R. I.; Schreiner, P. R.; Fokin, A. A.; Fokina, N. A; Dahl, J. E. P.; Carlson, R. M. K.; Vance, A. L.; Yang, W.; Terminello, L. J.; van Buuren, T.; Melosh, N. A.  Near-edge X-ray absorption fine structure spectroscopy of diamondoid thiol monolayers on gold.  J. Am. Chem. Soc. 2008, 130, 10536–10544.

80.  Chernish, L. V.; Gunchenko, P. A.; Barabash, A. B.; Goreslavets, V. S.; Yurchenko, A. G.; Fokin, A. A. Selective synthesis of 1,1-diadamantane monoderivatives.  Zhurn. Org. Pharm. Khim. 2008, 6, 48–51.

79.  Zhuk, T. S.; Gunchenko, P. A.; Korovai, Ya. Yu.; Schreiner,P. R.; Fokin A. A. Mechanisms of the C–H halogenation of adamantane in the presence of N-hydroxyphthalimide.   Theoret. and Experim. Khim.  2008, 44, 1, 46–51.

78.  Schwertfeger, H; Fokin, A. A.; Schreiner, P. R. Diamonds are a chemist’s best friend: Diamondoid chemistry beyond adamantane.  Angew. Chem. Int. Ed. 2008, 47, 1022–1036.

77.  Fokin, A. A.; Yurchenko, A. G.; Rodionov, V. N.; Gunchenko, P. A.; Yurchenko, R. I.; Reichenberg, A.; Wiesner, J.; Hintz, M.; Jomaa, H.; Schreiner, P.R. Synthesis of the antimalarial drug FR900098 utilizing the nitroso-ene reaction. Org. Lett. 2007, 9, 4379–4382. G

76.  Fokina, N. A.; Tkachenko, B. A.; Merz, A.; Serafin, M.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R. Hydroxy derivatives of diamantane, triamantane, and [121]tetramantane: Selective preparation of bis-apical derivatives. Eur. J. Org. Chem. 2007, 4738–4745.

75.  Butova, E. D.; Fokin, A. A.; Schreiner, P. R. Beyond the Corey reaction: One-Step diolefination of cyclic ketones. J. Org. Chem. 2007, 72, 5689–5696.

74.  Fokin, A. A.; Butova, E. D.; Chernish, L. V.; Fokina, N. A.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Simple preparation of diamondoid 1,3-dienes via oxetane ring opening. Org. Lett. 2007, 9, 2541–2544.0

73.  Yang, W. L.; Fabbri J. D.; Willey, T. M.; Lee, J. R. I.; Dahl, J. E.; Carlson, R. M. K.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Meevasana, W.; Mannella, N.; Tanaka, K.; Zhou, X. J.; van Buuren, T.; Kelly, M. A.; Hussain, Z.; Melosh, N. A.; Shen, Z.-X. Monochromatic electronphotoemission from diamondoid monolayers. Science 2007, 316, 1460–1462.

72.       Wodrich, M. D.; Corminboeuf, C.; Schreiner, P. R.; Fokin, A. A.; Schleyer, P. v. R. How accurate are DFT treatments of organic energies? Org. Lett. 2007, 9, 1851–1854.

71.  Schreiner, P. R.; Fokin, A. A.; Pascal, R. A., Jr.; de Meijere, A. Many density functional theory approaches fail to give reliable large hydrocarbon isomer energy differences. Org. Lett. 2006, 8, 3635–3638.

70.  Fokin, A. A.; Schreiner, P. R.; Fokina, N. A.; Tkachenko, B. A.; Hausmann, H.; Serafin, M. Dahl, J. E. P.; Liu, S.; Carlson, R. M. K.  Functionalized nanodiamonds Part 4: Reactivity of [1(2,3)4]pentamantane (Td-Pentamantane): A nanoscale model of diamond J. Org. Chem. 2006, 71, 8532–8540.

69.   Ponomarenko, M. V.; Serguchev Y. A.; Ponomarenko, B. V.; Röschenthaler, G.-V.; Fokin, A. A. Experimental and theoretical studies on the transannular cyclizations of 3,7-dimethylenebicyclo[3.3.1]nonane with polyfluoroalkyl radicals.  J. Fluor. Chem, 2006, 127, 842–849.

68.  Schreiner, P. R.; Fokina, N. A.; Tkachenko, B. A.; Hausmann, H.; Serafin, M.; Dahl, J. E. P.; Liu, S.; Carlson, R. M. K.; Fokin, A. A. Functionalized Nanodiamonds Part 2: Triamantane and [121]Tetramantane. J. Org. Chem. 2006, 71, 18, 6709–6720. This work is featured: Cover picture of the J. Org. Chem., 2006, issue 18.

67.  Tkachenko, B. A.; Fokina, N. A.; Chernish, L. V.; Dahl, J. E. P.; Liu, S.; Carlson, M. K.; Fokin, A. A.; Schreiner, P. R. Functionalized Nanodiamonds Part 3: Thiolation of tertiary/bridgehead alcohols. Org. Lett. 2006, 8, 1767–1770.

66.  Fokin, A. A.; Schreiner, P. R.; Berger, R.; Robinson, G. H.; Wei, P.; Campana, C. F. Pseudotetrahedral polyhalocubanes: Synthesis, structures, and parity violating energy differences. J. Am. Chem. Soc. 2006, 128, 5332–5333. This work is featured: Nature, 2006, 44, 4, 5.

65.  Fokin, A. A.; Tkachenko, B. A.; Gunchenko, P. A. Gusev, D. V. Schreiner, P. R. Functionalized Nanodiamonds Part I. An experimental assessment of diamantane and computational predictions for higher diamondoids. Chem. Eur. J. 2005, 11, 7091–7101.

64.  de Meijere, A.; Lee, C.-H.; Kuznetsov M. A.; Gusev, D. V.; Kozhushkov, S. I.; Fokin, A. A.; Schreiner, P. R. Preparation and reactivity of [D3d]-octahedrane: The most stable (CH)12 hydrocarbon. Chem. Eur. J. 2005, 11, 6175–6184.

63.  Rodionov, V. N.; Chernyaev, B. V.; Levandovskii, I. A.; Shubina, T. E.; Fokin, A. A..  Quantum-chemical interpretation of the reorientation of dialkyl-cis-9,10-dihydroanthracene-9,10-endofumarates on a silver-containing stationary phase.  Theoret. and Experim. Khim. 2005, 41, 1, 1–6.

62.  Rodionov, V. M.; Chernyaev, B. V.; Levandovs'kii, I. A.; Shubina, T. E.; Fokin, A. A.; Yurchenko, O. G.  Experimental and quantum-chemical study of the thermodynamics of complexation of methylbenzenes with silver(I) ion.    Naukovi Visti - Natsional'nii Tekhnichnii Universitet Ukraini "Kiivs'kii Politekhnichnii Institut"  2005, 1, 107–115.

61.  Fokin, A. A.; Tkachenko, B. A.; Gunchenko, P. A.; Schreiner, P. R. The protonation of cubane revisited. Angew. Chem. Int. Ed. 2005, 44, 146–149.

60.  Schreiner, P. R.; Fokin, A. A.; Kotke, M.; Weil, T. Noncovalent organocatalysis.  Ann. Pol. Chem. Soc. 2004, 3, part 1, 21–24.

59.  Schreiner, P. R.; Fokin, A. A. Selective alkane C–H-bond functionalizations utilizing oxidative single-electron transfer and organocatalysis. Chem. Record 2004, 3, 247–257.

58.  Kiriy, N.; Jahne, E.; Adler, H.-J.; Schneider, M.; Kiriy, A.; Gorodyska, G.; Minko, S.; Jehnichen, D.; Simon,|P.; Fokin, A. A.; Stamm, M. One-dimensional aggregation of regioregular polyalkylthiophenes. Nano Letters 2003, 3, 707–712.

57.  Gunchenko, P. A.; Vigovskaya, T. S.; Fokin, A. A.; Yurchenko, A. G. A New method for building of [3.3.3]propellan skeleton.  Ukr. Khim. Zhurn. 2003, 69, 10, 113–115.

56.  Fokin, A. A.; Schreiner, P. R. Metal-free, selective alkane functionalizations.  Adv. Chem. Cat. 2003, 345, 1035–1052.

55.  de Meijere, A.; Kozhushkov, S. I.; Fokin, A. A.; Emme, I.; Redlich, S.; Schreiner, P. R. New structurally interesting cyclopropane derivatives. A world of wonders and surprises. Pure Appl. Chem. 2003, 75, 549–562.

54.  Fokin, A. A.; Schreiner, P. R.; Kozhushkov, S. I.; Sattelmeyer, K. W.; Schaefer, H. F.; de Meijere, A. Delocalizations in s-radical cations: The Intriguing structures of ionized [n]rotanes.  Org. Lett. 2003, 5, 697–700.

53.  Tkachenko, B. A.; Shubina, T. E.; Gusev, D. V.; Gunchenko, P. A.; Yurchenko, A. G.; Schreiner, P. R.; Fokin, A. A. Mechanisms of C–H Activation of Alkanes by Chromium-oxo Reagents.  Theoret. and Experim. Khim. 2003, 39, 2, 90–95.

52.   Krasutsky, P. A.; Kolomitsyn, I. V.; Botov, E. M.; Carlson, R. M.; Semenova, I. G.; Fokin, A. A. Heterolytic decarboxylation involving acyltrifluoroacetyl peroxide intermediates. Tetrahedron Lett. 2002, 43, 8687–8691.

51.  Schreiner, P. R.; Fokin, A. A.; Lauenstein, O.;  Okamoto, Y.; Wakita, T.; Rinderspacher, C; Robinson, G. H.; Vohs, J. K.; Campana.; C. F. Pseudotetrahedral polyhaloadamantanes as chirality probes: Synthesis, separation, and absolute configuration.  J. Am. Chem. Soc. 2002, 124, 13348–13349.

50.  Fokin, A. A.; Tkachenko, B. A.; Shubina, T. E.; Gunchenko, P. A.; Gusev, D. V.; Vohs, J. K.; Robinson, R. H.; Yurchenko, A. G.; Schreiner, P. R. The protoadamantane radical cation.  Eur. J. Org. Chem. 2002, 3844–3849.

49.  Shubina, T. E.; Gunchenko, P. A.; Vigovskaya, T. S.; Schreiner, P. R.; Yurchenko, A. G.; Fokin, A. A.  [3.3.2]- and [3.3.3]propellanes in reactions with oxidizing electrophiles. Teoret. i Experim. Khimiya, 2002, 38, 4, 226–231.

46.  Kiriy, A. V.; Yurchenko, A. G.; Fokin, A. A. The new [2,3]-sigmatropic rearrangement of allylsulfinyl carbanions. Russ. J. Org. Chem. 2002, 38, 3, 471–472.

48.  Fokin, A. A.; Shubina, T. E.; Gunchenko, P. A.; Isaev, S. D.; Yurchenko, A. G.; Schreiner, P. R. H-Coupled electron transfer in alkane C–H activations with halogen electrophiles. J. Am. Chem. Soc. 2002, 124, 10718–10727.

47.  Fokin, A. A.; Schreiner, P. R. Selective alkane transformations via radicals and radical cations: Insights into the activation step from experiment and theory. Chem. Rev. 2002, 102, 1551–1593.

45.  Shubina, T. E.; Gunchenko. P. A.; Yurchenko, A. G.; Schreiner, P. R.; Butova, E. D.; Fokin, A. A. Structure and transformations of 1-alkyladamantane radical cations.  Teoret. i Experim. Khimiya 2002, 38, 1, 8–13.

44.  Schreiner, P. R.; Lauenstein, O.; Butova, E. D.; Gunchenko, P. V.; Kolomitsin, I. V.; Wittkopp, A.; Feder, G.; Fokin, A. A. Selective radical reactions in multiphase systems: Phase-transfer halogenations of alkanes. Chem. Eur. J. 2001, 7, 23, 4996–5003.

43.  Fokin, A. A.; Tkachenko, B. A.; Korshunov, O. I.; Gunchenko, P. A.; Schreiner, P. R. Molecule-induced alkane homolysis with dioxiranes. J. Am. Chem. Soc. 2001, 123, 11248–11252.

42.  Prall, M.; Wittkopp, A.; Fokin, A. A.; Schreiner, P. R.  Substituent effects on the Bergman Cyclization of (Z)-1,5-hexadiyne-3-enes: A systematic computational study. J. Comp. Chem. 2001, 22, 13, 1605–1614.

41.  Fornarini, S.; Crestone, E.; Fokin, A. A. The protonation of gaseous cyclopropane. Chem. Eur. J. 2001, 7, 2916–2921.

40.  Schreiner, P. R.; Gunchenko, P. A.; Wittkopp, A.; Yaroshinsky, A. I.; Peleshanko, S. A.; Fokin, A. A.  The rearrangement of the cubane radical cation in solution. Chem. Eur. J. 2001, 7, 2739–2744.

39.  Krasutsky, P. A.; Kolomitsyn, I. V.;  Kiprof, P.;  Carlson, R. M.;  Sydorenko, N. A.; Fokin, A. A.  A Consecutive double-Criegee rearrangement using TFPAA: Stepwise conversion of homoadamantane to oxahomoadamantanes.  J. Org. Chem. 2001, 66, 1701–1707.

38.  Fokin, A. A.; Lauenstein, O.; Gunchenko, P. A.; Schreiner, P. R.  Halogenation of cubane under phase-transfer conditions: Single and double C–H-bond substitution with conservation of the cage Structure.  J. Am. Chem. Soc.  2001, 123, 1842–1847.

37.  Fokin, A. A.; Peleshanko, S. A.; Gunchenko, P. A.; Gusev, D. V.; Schreiner, P. R. Hydrocarbon activations with cerium (IV) ammonium nitrate: Free radical versus oxidative pathways. Eur. J. Org. Chem. 2000, 3357–3362.

36.  Lauenstein, O.; Fokin, A. A.; Schreiner, P. R. A combined experimental and computational study of the H/D kinetic isotope effects for bromination and iodination of aliphatic hydrocarbons under phase-transfer conditions. Org. Lett.  2000, 2201–2204.

35.  Fokin,A. A.;Schreiner,P. R.; Gunchenko, P. A.; Peleshanko, S. A.; Shubina,T. E.; Isaev, S. D.; Tarasenko, P. V.; Kulik, N. I.; Schiebel, H.-M.; YurchenkoA. G. Oxidative single electron transfer activation of s-bonds in aliphatic halogenation reactions. J. Am. Chem. Soc. 2000, 122, 7317–7326.

34.  Fokin, A. A.; Kushko, A. O.; Kirij, A. V.; Yurchenko, A. G.; Schleyer, P. v. R. Direct transformations of ketones to g-unsaturated thiols via [2,3]-sigmatropic rearrangement of allyl sulfinyl carbanions: Combined experimental and theoretical study. J. Org. Chem. 2000, 65, 2984–2995.

33.  Kolomitsin, I. V.; Krasutsky, P. A.; Sidorenko, N. V.; Yurchenko, A. G.; Fokin, A. A.  Oxidative fragmentation of tetrahydrocyclopentadiene structure. Russ. J. Org. Chem. 2000,  36, 456–457.

32.  Krasutsky, P. A.; Kolomitsin, I. V.; Kiprof, P.; Carlson, R. M.; Fokin, A. A. Observation of a stable carbocation in a consecutive Criegee rearrangement with trifluoroperacetic acid. J. Org. Chem. 2000, 65, 3926–3933.

31.  Fokin, A.A.; Kiran, B.; Bremer, M.; Yang, X.; Jiao, H.; Schleyer, P. v. R.  Which electron count rules are needed for four-centered tree-dimensional aromaticity? Chem. Eur. J.; 2000, 6, 1615–1628.

30.  Schreiner, P. R.; Lauenstein, O.; Butova, E. D.; Fokin, A. A. The first efficient iodination of unactivated, aliphatic hydrocarbons. Angew. Chem. 1999, 111 2956–2958. Angew. Chem. Int. Ed. Engl. 1999, 38, 2786–2788. This work is featured: cover picture of the Angewandte Chemie, 1999, issue 18. Chemical and Engineering News 1999 September, 20, 44. Sueddeutsche Zeitung 1999 55, October, 12, p. V2/12.

29.  Fokin, A. A.; Gunchenko, P. A.; Peleshanko, S. A.; Schleyer, P. v. R.; Schreiner, P. R. Common radical cation intermediates in cage hydrocarbon activations.  Eur. J. Org. Chem. 1999, 855–860.

28.  Kushko, A. O.; Yurchenko, A. G.; Kirij, A. V.; Likhotvorik, I. R.; Fokin, A. A.  The novel one-step method of homoallylic tiols synthesis from ketons. Russ. J. Org. Chem. 1998, 34, 776–777.

27.  Fokin, A. A.; Schreiner, P. R.; Schleyer, P. v. R.; Gunchenko, P. A. Electrophilic and oxidative activation of the central C–C Bond in [3.3.n]Propellanes: A theoretical study. J. Org. Chem. 1998,No19, 6494–6502.

26.  Fokin, A. A.; Jiao, H.; Schleyer, P. v. R. From Dodecaheptapentaene to the “[n]Trannulenes”. A new In-plane aromatic family.  J. Am. Chem. Soc. 1998, 120, 9364–9365.

25.  Schreiner, P. R.; Lauenstein, O.; Kolomitsin, I. V.; Fokin, A. A.  Selective C–H activation of aliphatic hydrocarbon under phase-transfer conditions.  Angew. Chem.; Int. Ed. 1998, 37, 1895–1897. This paper was featured in Nachr. Chem. Tech. Lab. 1998 7/8, 706. Chemical and Engineering News 1998 July, 13, 55.

24.  Fokin, A. A.; Gunchenko, P. A.; Tkachenko, B. A.; Butova, E. D.; Yurchenko, A. G.  Backside activation of s-bonds with Cr(VI)-reagents.  Tetrahedron Lett. 1997, 38, 639–642.

23.  Fokin, A. A.; Gunchenko, P. A.; Kulik, N. I.; Iksanova, S. V.; Krasutsky, P. A.; Gogoman, I. V.; Yurchenko, A. G.  NO2+-containing reagents in the electrophilic and oxidative addition to propellanic C–C bond.  Tetrahedron 1996, 52, 5857–5866.

22.  Fokin, A. A.; Gunchenko, P. A.; Krasutsky, P. A.; Yaroshinsky, A. I.; Yurchenko, A. G. Oxidation of tetracyclo[4.3.1.1.4,801,4]undecane (1,4-cyclohomoadamantane). Russ. J. Org. Chem. 1995, 31, 796–797.

21.  Fokin, A. A.; Gunchenko, P. A.; Krasutsky, P. A.; Yaroshinsky, A. I.; Yurchenko, A. G. Oxidative addition to 3,6-dehydrohomoadamantane.  Tetrahedron Lett. 1995, 36, 4479–4482.

20.  Fokin, A. A.; Gagaeva, E. A.; Krasutsky, P. A.; Yurchenko, A. G. Stereoselective epoxidation of 4,7,7-trimethyl-3-oxabicyclo[3.3.1]hept-4-en-2-one. Russ. J. Org. Chem. 1994, 30, 940–941.

19.  Fokin, A. A.; Butova, E. D.; Kolomitsin, I. V.; Gagaeva, E. A.; Kornilov, A. M.; Sorochinsky A. E. Functional derivatives of 2-carene in cyclopropane-containing pyrethroides synthesis. Russ. J. Org. Chem. 1994, 30, 669–679.

18.  Fokin, A. A.; Butova, E. D.; Gulevitch, A. V.; Yurchenko, A. G.; Krasutsky, P. A.  Novel oxidative transformations in norpinonic acid synthesis. Russ. J. Org. Chem. 1993, 29, 1075–1076.

17.  Lichotvorik, I. R.; Litvin, A. L.; Shimko, R. I.; Fokin, A. A. The insertion of dichlorocarbene into tricyclo[5.2.1.02,5]decane structure. Vest. Kiev Polytech. Inst. 1992, 29, 3.

16.  Fokin, A. A.; Krasutsky, P. A.; Gulevich, A.V.; Yurchenko, A. G.  Oxidation of 3,7,7-trimethyl-3,4-dihydroxybicyclo[4.1.0]heptane by molecular oxygen. Russ. J. Org. Chem. 1992, 28, 1098–1099.

15.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structures of 1R-cis-polyhalogenchrysanthemic acids. Russ. J. Org. Chem. 1992, 28, 67–75.

14.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G.  Key synthones of pyrethrinoides based on 3-carene.  Ukr. Khim. Zhurnal 1992, 58, 1130–1135.

13.  Fokin, A. A.; Fedorenko, T. V.; Yurchenko, A. G. Enantioselective synthesis of chrysanthemic acid and derivatives. Ukr. Khim. Zhurnal 1992, 58, 1120–1126.

12.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structure of the stereoisomeric monochlorochrysanthemic acids. Russ. J. Org. Chem. 1991, 27, 1279–1283.

11.  Fokin, A. A.; Krasutsky, P. A.; Baula, O. P.; Yurchenko, A. G.  Functionalization of 4,7,7-trimethyl-3-oxabicyclo[3.31]hept-4-en-2-one with dichlorocarbene. Russ. J. Org. Chem. 1991, 27, 1363.

10.  Krasutsky, P. A.; Fokin, A. A.; Rodionov, V. N.; Kulik, N. I.; Ambrosienko, N. V.; Yurchenko, A. G.  On the mechanisms of transannular acidic cyclization of 3,7-dimethylenobicyclo[3.3.1]nonane and derivatives. Russ. J. Org. Chem. 1991, 27, 992–999.

9.      Krasutsky, P. A.; Fokin, A. A.; Butova, E. D.; Yurchenko, A. G. Stereoselective synthesis of (–)-pirocine and 1R-E-chrysanthemic acid from 2-pinene. Vest. Kiev. Polytech. Inst. 1991, 28, 40–44.

8.      Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G. The structures of carbenilation products of 2-pinene and 3-carene with carboethoxycarbene. Ukr. Khim. Zhurnal 1989, 55,  842–845.

7.      Krasutsky, P. A.; Fokin, A. A.; Maleev, A. V.; Kurkutova, E. N.; Struchkov, Y. T.; Yurchenko, A. G. The structure of adducts of allenes of bicyclo[3.3.1]nonane series with dihalocarbenes. Russ. J. Org. Chem. 1990, 26, 1016–1024.

6.      Krasutsky, P. A.; Fokin, A. A.; Skoba, E. D.; Yurchenko, A. G. the synthesis and protic cyclization of 3-vinylidenobicyclo[3.3.1]nonane-7-one. Russ. J. Org. Chem. 1986, 22, 460–461.

5.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and protic cyclization of 3-vinylideno-7-propadienilidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1986, 22, 459–460.

4.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and reactivity of 3-methylene-7-vinylidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1985, 21, 2522–2626.

3.      Krasutsky, P. A.; Fokin, A. A.; Kulik, N. I.; Yurchenko, A. G. The reactivity of 3,7-divinylidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1985, 21, 2518–2522.

2.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G.; Chekmenyova, L. A. The synthesis of 3,7-divinylidenbicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1984, 20, 1807–1808.

1.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G.; Jones, M. Jr.; Antipin, M. Y.; Struchkov, Y. T. The structure of carbenylation products of 3-methylenebicyclo[3.3.1]nonane. Teoret. i Experim. Khimiya 1984, 20, 427–433.

 

159. Becker, J.; Zhyhadlo, Y. Y.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Ferster, M.; Holthausen, M. C.; Specht, P.; Schindler, S.  Aerobic aliphatic hydroxylation reactions by copper complexes: A simple clipandcleave concept. Chem. Eur. J.2018, 24, https://doi.org/10.1002/chem.201802607

158.Gebbie, M. A.; Ishiwata, H.;  McQuade P.J.; Petrak, V.: Taylor, A.; Freiwald, C.; Dahl, J. E.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Nesladek, M.; Melosh, N. A. Experimental measurement of the diamond nucleation landscape reveals classical and nonclassical features. PNAS, 2018, 115, 33, 8284–8289.

157. Moncea, O.; Poinsot, D.; Fokin, A. A.; Schreiner, P. R.; Hierso, J. C. Palladium-catalyzed C2-H arylation of unprotected (N-H)-indoles “On water” using primary diamantyl phosphine oxides as a class of primary phosphine oxide ligands. ChemCatChem, 2018, 10, 2915 – 2922.

155.Hoc, N. T.  Fokin, A. A; Rodionov, V. N. Towards 3-(2-adamantylidene)diamantane derivatives through the McMurry cross coupling reaction. Org. Commun. 2018, 11, 2x, 75-79.

156. Hoc, N. T.  Fokin, A. A; Rodionov, V. N. Synthesis of 10-methoxydiamantan-3-one. MOLBANK. 2018, 2, UNSP M990. DOI: 10.3390/M990

154.Yan, H.;Narasimha, K. T.; Denlinger, J.;Li, F. H.;Mo, S.-K.;Nathan Hohman, J.;  Dahl, J. E. P.; ,Carlson, R. M. K.;Tkachenko, B. A.;Fokin, A. A.; Schreiner, P. R.; Hussain, Z.; Shen, Z.-X.; ,Melosh, N. A.Monochromatic photocathodes from graphene-stabilized diamondoids. Nano Lett., 2018, 18, 1099–1103.

153.Yan, H.; Yang, F.; Pan, D.; Lin, Y.; Hohman, J. N.; Solis-Ibarra, D.; Li, F. H.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Galli, G.; Mao, W. L.; Shen Z.-X.; Melosh, N. M. Sterically controlled mechanochemistry under hydrostatic pressure. Nature 2018, 554, 505–510.

152.Gunawan, M. A.; Moncea, O.; Poinsot, D.; Keskes, M.; Domenichini, B.; Heintz, O.; Chassagnon, R.; Herbst, F.; Carlson, R. M. K.; Dahl, J. E. P.; Fokin, A. A.; Schreiner, P. R.; Hierso,  J.-C. Nanodiamond-Palladium Core–Shell Organohybrid Synthesis: A Mild Vapor-Phase Procedure Enabling Nanolayering Metal onto Functionalized sp3-Carbon. Adv. Funct. Mater. 2018, 1705786 (15 p).

151.Gunchenko, P. A.; Li,J.; Liu, B.; Chen, H.; Pashenko, A. P.;Bakhonsky, V. V.; Zhuk. T. S.; Fokin, A. A. Aerobic oxidations with N-hydroxyphthalimide in trifluoroacetic acid. Molec. Cat. 2018, 446, 72-79.

150.Zhyhadlo, Y. Y.; Gaidai, A. V.; Sharapa, D. I.; Mitlenko, A. G.; Shishkin, O. V.; Shishkina, S. V.; Levandovskiy, I. A.; Fokin, A. A. Functionalised Cookson's diketones in chlorosulfonic acid: Towards polysubstituted D3-trishomocubanes. J. Chem. Res. 2017, 41, 12, 677-733.

149.Tyborski, C.; Gillen, R.; Fokin, A. A.; Koso, T. V.; Fokina, N. A.; Hausmann, H.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. Electronic and Vibrational Properties of Diamondoid Oligomers. J. Phys. Chem. 2017, 121, 48, 27082–27088

148.     Fokin, A. A.: Zhuk, T. S.; Blomeyer, S.; Peŕez, C.;  Chernish, L.V.; Pashenko, A. E.; Antony, J.; Vishnevskiy, Y. V.;  Berger, R. J. F.; Grimme, S.; Logemann, C.; Schnell, M.; Mitzel N. W.; Schreiner P. R. Intramolecular London dispersion interaction effects on gas-phase and solid-state structures of diamondoid dimers. J. Amer. Chem. Soc. 2017, 139, 16696-16707.

147.     Tyborski, C.; Meinke, R.; Gillen, R.; Bischoff, T.; Knecht, A.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N. Schreiner, P. R.; Moller, T.; Rander, T.; Thomsen, C.; Maultzsch, J. From isolated diamondoids to a van-der-Waals crystal: A theoretical and experimental analysis of a trishomocubane and a diamantane dimer in the gas and solid phase. J. Chem. Phys. 2017, 147, 4, 044303 (6 p.)

146.     Fokin, A. A.; Pashenko, A. E.; Bakhonsky, V. V.; Zhuk. T. S.; Chernish. L. V.; Gunchenko, P. A.; Kushko, A. O.; Becker, J.; Wende, R. C.; Schreiner. P. R. Chiral building blocks based on 1,2-disubstituted diamantanes. Synthesis, 2017. 49, 20032008.

145.     Yan, H.; Hohman, J. N.; Li, F. H.; Jia, C.; Solis-Ibarra, D.; Wu, B.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Vailionis, A.; Kim, T. R.; Devereaux, T. P.; Shen, Z.-X.; Melosh. N. A. Hybrid metal–organic chalcogenide nanowires with electrically conductive inorganic core through diamondoid-directed assembly. Nat. Mater. 2017, 16, 349–355.

144.  Hoc, N. T.;Kushko, A. O.;Fokin, A. A.;Rodionov, V. N. Functional derivatives of diamantanone. Russ. J. Org. Chem. 2016, 52, 8, 1209–1211.

143.Moncea O.; Gunawan, M. A.; Poinsot,D.; Cattey. H.;Becker,J.;Yurchenko,R. I.; Butova,E. D.; Hausmann,H.; Šekutor,M.; Fokin, A. A.; Hierso,J.-C.; Schreiner, P. R. Defying stereotypes with nanodiamonds: Stable primary diamondoid phosphines,  J. Org. Chem. 2016, 81, 8759−8769.

142.     Tverdiy, D. O. Chekanov, M. O.; Savitskiy, P. V.; Syniugin, A. R.; Yarmoliuk, S. M. Fokin, A. A. Efficient preparation of imidazo[1,5-a]pyridine-1-carboxylic acids. Synthesis 2016, 48, A–I.

141.     Ponomarenko, M. V.; Grabowsky,S.; Pal,R.; Röschenthaler, G.-V., Fokin, A. A. SF5-Enolates in Ti(IV)-mediated aldol reactions. J. Org. Chem. 2016, 81, 6783−6791.

140.     Karthik, T. N.; Ge,C.; Fabbri,J. D.; Clay,W.; Tkachenko, B. A.; Fokin, A.A.; Schreiner, P. R.; Dahl, J. E.; Carlson, R. M. K.; Shen, Z. X.; Melosh, N. A. Ultra-low effective work function surfaces using diamondoid monolayers. Nature Nanotech. 2016, 11, 267–273.

139.     Zhang, J. L.; Ishiwata, H.; Babinec, T. M.; Radulaski, M.; Müller, K.; Lagoudakis, K. G.; Dory, C.; Dahl, J.; Edgington, R.; Soulière, V.; Ferro, G.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N.; Vuckovic, J. Hybrid group IV nanophotonic structures incorporating diamond silicon-vacancy color centers. Nano Lett. 2016, 16, 212−217.

138.Syniugin, A. R.; Chekanov, M. O.; Savitskiy, P. V.; Pashenko, A. E.; Zhuk, T. S.; Yarmoluk, S. M.; Fokin, A A. New method for the synthesis of pyrrolo[2,3-b]dihydroquinolines. Tetrahedron Lett.  2016, 57, 213–215.

137.Valentin, L.; Henss, A.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Becker, S.; Würtele, C.; Schindler, S. Transition metal complexes with cage-opened diamondoid tetracyclo[7.3.1.14,12.02,7]tetradeca-6.11-diene. J. Coor. Chem. 2015, 68, 3295–3301.

136.Lourie, L. F.; Serguchev, Yu. A.; Bentya, A. V.; Ponomarenko, M. V.; Rusanov, E. B.; Vovk, M. V.; Fokin, A. A.; Ignat’ev, N. V. Metal free electrophilic fluoro-cyclization of unsaturated N-hydroxy- and N-acetoxyamides with N–F reagents. J. Fluor. Chem. 2015, 179, 42–47.

135.Bremer, M.; Untenecker, H.; Gunchenko, P. A.; Fokin, A. A.; Schreiner P. R.  Inverted carbon geometries: Challenges to experiment and theory. J. Org. Chem. 2015, 80, 6520−6524.

134.     Zhuk, T. S.; Koso, T.; Pashenko, A. E.; Hoc, N. T.; Rodionov, V. N.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Toward an understanding of diamond sp2-defects with unsaturated diamondoid oligomer model. J. Am. Chem. Soc. 2015, 137, 6577−6586.

133.     Gunawan, M. A.; Poinsot, D.; Domenichini, B.; Dirand, C.; Chevalier, S.; Fokin, A. A.; Schreiner, P. R.; Hierso, J.-P. The functionalization of nanodiamonds (diamondoids) as a key parameter of their easily controlled self-assembly in micro- and nanocrystals from the vapor phase. Nanoscale, 2015, 7, 1956–1962.

132.     Barabash, A. V.; Didukh, N. A.; Kibal’nyi, N. A.; Butova, E. D.; Schreiner, P. R.;Fokin, A. A. Unusual aerobic oxidation of sterically hindered 1-diamanty methyl ketone. Russ. J. Org. Chem. 2014, 50, 1690–1691.

131.       Gunchenko, P. A.; Novikovskii, A. A.; Byk, M. V.; Fokin, A. A.  Structure and transformations of diamantane radical cation: Theory and experiment. Russ. J. Org. Chem. 2014, 50, 1749–1754.

130.Mishura, A. M.; Sklyarova, A. S.; Shamota, T. V.: Rodionov, V. N.; Fokin, A. A.  Preparative synthesis of pentacyclo[6.3.0.02,6.03,10.05,9]undecan-4-one (D3-Trishomocubanone). Russ. J. Org. Chem. 2014, 50, 1542–1544.

129.Barabash, A. V.; Butova, E. D.; Kanyuk, I. M.; Schreiner, P. R.; Fokin, A. A. Beyond the Corey reaction II: Dimethylenation of sterically congested ketones J. Org. Chem. 2014, 79, 10669−10673. ACS Editor’s Choice, 01.10.2014.

128.Randel, J. C.; Niestemski, F. C.; Botello-Mendez, A. R.; Mar, W.; Ndabashimiye, G.; Melinte, S.; Dahl, J. E. P.; Carlson R. M. K.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Charlier, J.-C.; Manoharan, H. C. Unconventional molecule-resolved current rectification in diamondoid fullerene hybrids. Nature Comm. 2014, 5, 4877 (6 p).

127.Tchernobaev, I. I.; Serguchev, Yu. A.; Fokin, A. A. Mechanism and selectivities of the chlorination of toluene in the presence of catalytical composition antimony pentachloride – benzodithio crown ether. Ukr. Krim. Zhurn. 2014, 50, 45–49.

126.Ponomarenko, M. V.; Serguchev, Yu. A.; Hirschberg, M. E.; Röschenthaler, G.-V.; Fokin, A. A. Elemental F2 with transannular dienes: Regioselectivities and mechanisms. Chem. Eur. J. 2014, 20, 10383–10391.

125.Fokin, A.A.; Yurchenko, R. I.; Tkachenko,B.A.; Fokina,N. A.; Gunawan,M. A.; Poinsot,D.; Dahl, J. E. P.; Carlson,R. M. K.; Serafin,M.; Cattey,H.; Hierso,J.-C.; Schreiner, P. R. Selective preparation of diamondoid phosphonates. J. Org. Chem. 2014, 79, 5369–5373.

124.Fokin, A. A.; Zhuk, T. S.; Pashenko, A. E.; Osipov, V. V.; Gunchenko,P. A.; Serafin, M.; Schreiner, P. R. Functionalization of homodiamantane: Oxygen insertion reactions without rearrangement with dimethyldioxirane. J. Org. Chem. 2014, 79, 1861–1866.

123.Meinke, R.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. UV resonance Raman analysis of trishomocubane and diamondoid dimers. J. Chem. Phys. 2014, 140, 034309 (5p).

122.Kahl, P.; Tkachenko, B. A.; Novikovsky, A. A.; Backer, J.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.  Efficient peparation of aically substituted damondoid drivatives, Synthesis 2014, 46, 787–798.

121.Gunawan, M. A.; Hierso, J.-C.; Poinsot, D.; Fokin, A. A.; Fokina, N. A.; Tkachenko, B. A.;Schreiner, P. R. Diamondoids: Functionalization and subsequent applications of perfectly defined molecular cage hydrocarbons. New J. Chem. 2014, 38, 28–41.

120.     Chekanov, M. O.; Ostrynska, O. V.; Tarnavskyi, S. S.; Synyugin, A. R.; Briukhovetska, N. V.; Bdzhola, V. G.; Pashenko, A. E.; Fokin A. A.; Yarmoluk, S. M. Design, synthesis and biological evaluation of 2-aminopyrimidinones and their 6-aza-analogs as a new class of СК2 inhibitors. J. Enz. Inhib. Med. Chem. 2014, 29, 5, 639­–646.

119.     Ponomarenko, M. V.; Lummer, K.; Fokin, A. A.; Serguchev, Yu. A.; Bassil,B. S.; Röschenthaler, G.-V.  Preparations of SF5- and CF3-substituted arenes utilizing the 7-oxabicyclo­[2.2.1]hept-2-ene synthones. Org. Biomol. Chem. 2013, 11, 8103­–8112.

118.     Kacharov, A. D.; Yemets, S. V.; Nemykin,V. N.; Kacharova, L. M.; Fokin,A. A.; Krasutsky, P. A. Stereoselectivity of A-ring contraction for 3-oxotriterpenoids.  RCS Advances 2013, 3, 19057–19063.

117.     Mishura,A. M.; Sklyarova,A. S.; Sharapa, D. I.; Levandovsky, I. A.; Serafin, M.; Fokin, A. A.; Rodionov, V. N. Stereoselective Preparation of mono- and bis-derivatives of pentacyclo[6.3.0.02,6.03,10.05,9]undecane (D3-trishomocubane). Open. Chem.  2013, 11, 2144–2150.

116.Li, F. H.; Fabbri, J. D.; Yurchenko, R. I.; Mileshkin, A. N.; Hohman, J. N.; Yan, H.; Yuan, H.; Tran, I. C.; Willey, T. M.; Bagge-Hansen, M.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N. A. Covalent attachment of diamondoid phosphonic acid dichlorides to tungsten oxide surfaces. Langmuir 2013, 29, 9790–9797.

115.Zimmermann, T.; Richter, R.; Knecht, A.; Fokin, A. A.; Koso, T. V.; Chernish, L. V.; Gunchenko, P. A.; Schreiner, P. R.; Moller, T.; Rander, T. Exploring covalently bound diamondoid aggregates with valence photoelectron spectroscopy. J. Chem. Phys. 2013, 139, 084310 (6 p).

114.Fokin, A. A.; Butova, E. D.; Barabash, A. V; Huu, N. N.; Tkachenko. B. A.; Fokina, N. A.; Schreiner, P. R. Preparative synthesis of vinyl diamondoids. Synth. Comm. 2013, 43, 1772–1777.

113.Sklyarova, A. S.; Rodionov, V. N.; Parsons, C. G.; Quack, G.; Schreiner, P. R.; Fokin, A. A. Preparation and testing of homocubyl amines as therapeutic NMDA receptor antagonists. Med. Chem. Res. 2013, 22, 360–366.

112.     Clay, W. A.; Maldonado, J. R.;  Pianetta, P.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Melosh, N.; Shen, Z.-X. Photocathode device using diamondoid and cesium bromide films Appl. Phys. Lett. 2012, 101, 241605 (5p).

111.Ishiwata, H.; Acremann, Y.; Scholl, A.; Rotenberg, E.; Hellwig, O.; Dobisz, E.; Doran, A.; Tkachenko, B.A.; Fokin, A.A.; Schreiner, P.R.; Dahl, J.E.P.; Carlson, R.M.K.; Melosh, N.; Shen, Z.-X.; Oldag, H. Diamondoid coating enables disruptive approach for chemical and magnetic imaging with 10 nm spatial resolution. Appl. Phys. Lett. 2012, 101, 163101 (5 p).

110.Fokin, A. A.;  Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Hausmann, H.; Serafin, M.; Dahl J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Stable alkanes containing very long carbon–carbon bonds. J. Am. Chem. Soc. 2012, 134, 1364113650.

109.     Gunchenko, P. A.; Fokin, A. A. Mechanisms of activation of C–H bonds in framework compounds: Theory and experiment. Theoret. Experim. Khim. 2012, 47, 6, 343–360.

108.     Gaidai, A. V.; Volochnyuk, D. M.; Shishkin, O. V.; Fokin, A. A.; Levandovskiy, I. A.; Shubina, T. E. D3-Trishomocubane-4-carboxylic acid as a new chiral building block: Synthesis and absolute configuration. T. E. Synthesis 2012, 44, 810–816.ю

107.Fokina, N. A.; Tkachenko, B. A.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner P. R.  Synthesis of diamondoid carboxylic acid. Synthesis 2012, 44, 259–264.1

106.Fokin, A. A.; Gerbig, D.; Schreiner, P. R. σ/σ- and π/π-Interactions are equally important: multilayered graphanes. J. Am. Chem. Soc. 2011, 133, 20036–20039.

105.Rodionov, V. N.; Sklyarova, A. S.; Shamota, T. V.; Schreiner, P. R.; Fokin, A. A. Selective reductive dimerization of homocubane series oximes. Russ. J. Org. Chem. 2011, 47, 11, 1695−1702.

104.     Schreiner, P. R.; Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Hausmann, H.; Serafin, M.; Schlecht, S.; Dahl J. E. P.; Carlson, R. M. K.; Fokin, A. A. Overcoming  lability of extremely long alkane carbon–carbon bonds through dispersion forces. Nature 2011, 477, 308–311. This paper was featured in Chemical & Engineering News, 89(38), September 19, 2011 [Science & Technology, Concentrates]

103.Novikovskii, A. A.; Gunchenko P. A.; Prikhodchenko P. G.; Serguchev, Yu. A.; Schreiner P. R.; Fokin A.A. Comparative theoretical and experimental analysis of hydrocarbon σ-radical cations. Russ. J. Org. Chem. 2011, 47, 1293–1299.

102.     Shubina, T. E.; Fokin, A. A. Hydrocarbon s-radical cations. WIREs Comput. Mol. Sci. 2011, 1 661679.

101.     Serguchev, Yu. A.; Ponomarenko, M. V.; Lourie, L. F.; Fokin, A. A. Transannular additions of selectfluor and xenon difluoride: regioselectivity and mechanism. J. Phys. Org. Chem. 2011, 24, 407–413.

100.     Butova, E. D.; Barabash, A. V.; Petrova, A. A.; Kleiner, C. M.; Schreiner, P. R.; Fokin. A. A. Stereospecific consecutive epoxide ring expansion with dimethylsulfoxonium methylide, J. Org. Chem. 2010, 75, 18, 6229–6235.

99.    Demchenko, P. Yu.; Gladyshevskii, R. E.; Volkov, S. V.; Kharkova, L. B.; Yanko, O. G.; Fokina, Z. A.; Fokin, A. A. The first nonaselenium ring. Chem. Commun. 2010, 46, 4520–4522.

98.  Lysenko, A. B.; Senchyk, G. A.; Lincke, J.; Lässig, D.; Fokin, A. A.; Butova, E. D.; Schreiner, P. R.; Krautscheid, H.; Domasevitch, K. V. Metal oxide-organic frameworks (MOOFs), a new series of coordination hybrids constructed from molybdenum(VI) oxide and bitopic 1,2,4-triazole linkers. Dalton Trans. 2010, 39, 4223–4231.

97.  Zhuk, T. S.; Bratko, E. Y.; Pashenko, A. E.; Gunchenko, P. A.; Yurchenko, A. G.; Schreiner, P. R.; Fokin, A. A. The “green” synthesis of neuroprotecting drug Memantine. J. Org. Pharm. Chem. 2010, 8, 62–66.

96.  Roth, S.; Leuenberger, D.; Osterwalder, J.; Dahl, J. E.; Carlson, R. M. K.; Tkachenko, B. A. Fokin, A. A.; Schreiner, P. R., Hengsberger, M. Negative-electron-affinity diamondoid monolayers as high-brilliance source for ultrashort electron pulses. Chem. Phys. Lett.  2010, 495, 102–108.

95.  Landt, L.; Bostedt, C.; Wolter, D.; Möller, T.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Kulesza, A.; Bonacic-Koutecky, V. Experimental and theoretical studies of the absorption properties of thiolated diamondoids. J. Chem. Phys. 2010, 132, 144305 (6p).

94.  Landt, L.; Staiger, M.; Wolter, D.; Klünder, K.; Zimmermann, P.; Willey, T. M.; van Buuren, T.; Brehmer, D.; Schreiner, P. R.; Tkachenko, B. A.; Fokin, A. A.; Möller, T.; Bostedt, C. The influence of a single thiol group on the electronic and optical properties of the smallest diamondoid adamantane. J. Chem. Phys. 2010, 132, 0247101(7p).

93.  Levandovskiy, I. A.; Shubina, T. E.; Fokin, A. A. Computational and QSAR study of the alkylnaphthyl ketones adsorption on silver-ion stationary phase.  J. Molec. Mod. 2010, 16, 513–522.

92.  Schreiner, P. R.; Fokin, A. A.; Reisenauer, H. P.;  Tkachenko, B. A.; Vass, E.; Olmstead, M. M.; Bläser, D.; Boese, R.; Dahl, J. E. P.; Carlson, R. M. K. [123]Tetramantane: Parent of a new family of σ-helicenes. J. Am. Chem. Soc. 2009, 131, 11292–11293.

91.  Fokin, A. A.; Gunchenko, P. A.; Novikovsky, A. A.; Shubina, T. E.; Chernyaev, B. V.; Dahl J. E. P.; Carlson, R. M. K.; Yurchenko, A. G.; Schreiner P. R. Photoacetylation of diamondoids: Selectivities and mechanism. Eur. J. Org. Chem. 2009, 5153–5161. This work is featured: Cover picture of the Eur. J. Org. Chem., 2009, issue 30.

90.  Fokin, A. A.; Zhuk, T. S.; Pashenko, A. E.; Dral, P. O.; Gunchenko, P. A.;Dahl, J. E. P.;Carlson, R. M. K.;Koso, T. V.;Serafin, M.; Schreiner, P. R. Oxygen-doped nanodiamonds: Synthesis and functionalizations. Org. Lett. 2009, 11, 3068–3071.

89.  Sklyarova, A. S.; Rodionov, V. N.; Fokin, A. A. A convenient preparative synthesis of pentacyclo[5.3.0.02,5.03,9.04,8]decane (C2-bishomocubane). Russ. J. Org. Chem. 2009, 45, 11, 1644−1647.

88.  Gunchenko, P. A.; Makuhina, A. M.; Novikovsky, A. A.; Yurchenko, A. G.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Structure and transformations of homoadamantane radical cation.  Theoret. and Experim. Khim. 2009, 45, 4, 246–251.

87.  Willey, T. M.; Lee, J. R. I.; Fabbri, J. D.; Wang, D.; Nielsen, M. H.; Randel, J. C.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Dahl, J. E. P.; Carlson, R. M. K.; Terminello, L. J.; Melosh, N. A.; van Buuren, T. Determining orientational structure of diamondoid thiols attached to silver using near-edge X-ray absorption fine structure spectroscopy. J. Elec. Spectr. Rel. Phen. 2009, 172, 69–77.

86.  Schwertfeger, H.; Würtele, C.; Hausmann, H.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R. Selective preparation of diamondoid fluorides. Adv. Synth. Catal. 2009, 351, 1041–1054.

85.  Fokin, A. A.; Schreiner, P. R. Band gap tuning in nanodiamonds: First principle computational studies. Molec. Phys. 2009, 107, 8–12, 823–830.

84.  Fokin, A. A.; Tkachenko, B. A.; Fokina, N.  A.; Hausmann, H.; Serafin, M.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Reactivities of the prism-shaped diamondoids [1(2)3]tetramantane and [12312]hexamantane (cyclohexamantane). Chem. Eur. J. 2009, 15, 3851–3862.

83.  Fokin, A. A.; Merz, A.; Fokina, N. A.; Schwertfeger, H.; Liu, S. L.; Dahl, J. E. P.; Carlson, R. K. M.; Schreiner, P. R.  Synthetic routes to aminotriamantanes, topological analogues of the neuroprotector memantine. Synthesis 2009, 909–912.

82.  Clay, W. A.; Liu, Z.; Yang, W.; Fabbri, J. D.; Dahl, J. E.; Carlson, R. M. K.; Sun, Y.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Pianetta, P. A.; Melosh, N.; Shen Z.-X. Origin of the monochromatic photoemission peak in diamondoid monolayers. Nano Lett. 2009, 9, 57–61.

81.  Willey, T. M.; Fabbri, J. D.; Lee, J. R. I.; Schreiner, P. R.; Fokin, A. A.; Fokina, N. A; Dahl, J. E. P.; Carlson, R. M. K.; Vance, A. L.; Yang, W.; Terminello, L. J.; van Buuren, T.; Melosh, N. A.  Near-edge X-ray absorption fine structure spectroscopy of diamondoid thiol monolayers on gold.  J. Am. Chem. Soc. 2008, 130, 10536–10544.

80.  Chernish, L. V.; Gunchenko, P. A.; Barabash, A. B.; Goreslavets, V. S.; Yurchenko, A. G.; Fokin, A. A. Selective synthesis of 1,1-diadamantane monoderivatives.  Zhurn. Org. Pharm. Khim. 2008, 6, 48–51.

79.  Zhuk, T. S.; Gunchenko, P. A.; Korovai, Ya. Yu.; Schreiner,P. R.; Fokin A. A. Mechanisms of the C–H halogenation of adamantane in the presence of N-hydroxyphthalimide.   Theoret. and Experim. Khim.  2008, 44, 1, 46–51.

78.  Schwertfeger, H; Fokin, A. A.; Schreiner, P. R. Diamonds are a chemist’s best friend: Diamondoid chemistry beyond adamantane.  Angew. Chem. Int. Ed. 2008, 47, 1022–1036.

77.  Fokin, A. A.; Yurchenko, A. G.; Rodionov, V. N.; Gunchenko, P. A.; Yurchenko, R. I.; Reichenberg, A.; Wiesner, J.; Hintz, M.; Jomaa, H.; Schreiner, P.R. Synthesis of the antimalarial drug FR900098 utilizing the nitroso-ene reaction. Org. Lett. 2007, 9, 4379–4382. G

76.  Fokina, N. A.; Tkachenko, B. A.; Merz, A.; Serafin, M.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R. Hydroxy derivatives of diamantane, triamantane, and [121]tetramantane: Selective preparation of bis-apical derivatives. Eur. J. Org. Chem. 2007, 4738–4745.

75.  Butova, E. D.; Fokin, A. A.; Schreiner, P. R. Beyond the Corey reaction: One-Step diolefination of cyclic ketones. J. Org. Chem. 2007, 72, 5689–5696.

74.  Fokin, A. A.; Butova, E. D.; Chernish, L. V.; Fokina, N. A.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Simple preparation of diamondoid 1,3-dienes via oxetane ring opening. Org. Lett. 2007, 9, 2541–2544.0

73.  Yang, W. L.; Fabbri J. D.; Willey, T. M.; Lee, J. R. I.; Dahl, J. E.; Carlson, R. M. K.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Meevasana, W.; Mannella, N.; Tanaka, K.; Zhou, X. J.; van Buuren, T.; Kelly, M. A.; Hussain, Z.; Melosh, N. A.; Shen, Z.-X. Monochromatic electronphotoemission from diamondoid monolayers. Science 2007, 316, 1460–1462.

72.       Wodrich, M. D.; Corminboeuf, C.; Schreiner, P. R.; Fokin, A. A.; Schleyer, P. v. R. How accurate are DFT treatments of organic energies? Org. Lett. 2007, 9, 1851–1854.

71.  Schreiner, P. R.; Fokin, A. A.; Pascal, R. A., Jr.; de Meijere, A. Many density functional theory approaches fail to give reliable large hydrocarbon isomer energy differences. Org. Lett. 2006, 8, 3635–3638.

70.  Fokin, A. A.; Schreiner, P. R.; Fokina, N. A.; Tkachenko, B. A.; Hausmann, H.; Serafin, M. Dahl, J. E. P.; Liu, S.; Carlson, R. M. K.  Functionalized nanodiamonds Part 4: Reactivity of [1(2,3)4]pentamantane (Td-Pentamantane): A nanoscale model of diamond J. Org. Chem. 2006, 71, 8532–8540.

69.   Ponomarenko, M. V.; Serguchev Y. A.; Ponomarenko, B. V.; Röschenthaler, G.-V.; Fokin, A. A. Experimental and theoretical studies on the transannular cyclizations of 3,7-dimethylenebicyclo[3.3.1]nonane with polyfluoroalkyl radicals.  J. Fluor. Chem, 2006, 127, 842–849.

68.  Schreiner, P. R.; Fokina, N. A.; Tkachenko, B. A.; Hausmann, H.; Serafin, M.; Dahl, J. E. P.; Liu, S.; Carlson, R. M. K.; Fokin, A. A. Functionalized Nanodiamonds Part 2: Triamantane and [121]Tetramantane. J. Org. Chem. 2006, 71, 18, 6709–6720. This work is featured: Cover picture of the J. Org. Chem., 2006, issue 18.

67.  Tkachenko, B. A.; Fokina, N. A.; Chernish, L. V.; Dahl, J. E. P.; Liu, S.; Carlson, M. K.; Fokin, A. A.; Schreiner, P. R. Functionalized Nanodiamonds Part 3: Thiolation of tertiary/bridgehead alcohols. Org. Lett. 2006, 8, 1767–1770.

66.  Fokin, A. A.; Schreiner, P. R.; Berger, R.; Robinson, G. H.; Wei, P.; Campana, C. F. Pseudotetrahedral polyhalocubanes: Synthesis, structures, and parity violating energy differences. J. Am. Chem. Soc. 2006, 128, 5332–5333. This work is featured: Nature, 2006, 44, 4, 5.

65.  Fokin, A. A.; Tkachenko, B. A.; Gunchenko, P. A. Gusev, D. V. Schreiner, P. R. Functionalized Nanodiamonds Part I. An experimental assessment of diamantane and computational predictions for higher diamondoids. Chem. Eur. J. 2005, 11, 7091–7101.

64.  de Meijere, A.; Lee, C.-H.; Kuznetsov M. A.; Gusev, D. V.; Kozhushkov, S. I.; Fokin, A. A.; Schreiner, P. R. Preparation and reactivity of [D3d]-octahedrane: The most stable (CH)12 hydrocarbon. Chem. Eur. J. 2005, 11, 6175–6184.

63.  Rodionov, V. N.; Chernyaev, B. V.; Levandovskii, I. A.; Shubina, T. E.; Fokin, A. A..  Quantum-chemical interpretation of the reorientation of dialkyl-cis-9,10-dihydroanthracene-9,10-endofumarates on a silver-containing stationary phase.  Theoret. and Experim. Khim. 2005, 41, 1, 1–6.

62.  Rodionov, V. M.; Chernyaev, B. V.; Levandovs'kii, I. A.; Shubina, T. E.; Fokin, A. A.; Yurchenko, O. G.  Experimental and quantum-chemical study of the thermodynamics of complexation of methylbenzenes with silver(I) ion.    Naukovi Visti - Natsional'nii Tekhnichnii Universitet Ukraini "Kiivs'kii Politekhnichnii Institut"  2005, 1, 107–115.

61.  Fokin, A. A.; Tkachenko, B. A.; Gunchenko, P. A.; Schreiner, P. R. The protonation of cubane revisited. Angew. Chem. Int. Ed. 2005, 44, 146–149.

60.  Schreiner, P. R.; Fokin, A. A.; Kotke, M.; Weil, T. Noncovalent organocatalysis.  Ann. Pol. Chem. Soc. 2004, 3, part 1, 21–24.

59.  Schreiner, P. R.; Fokin, A. A. Selective alkane C–H-bond functionalizations utilizing oxidative single-electron transfer and organocatalysis. Chem. Record 2004, 3, 247–257.

58.  Kiriy, N.; Jahne, E.; Adler, H.-J.; Schneider, M.; Kiriy, A.; Gorodyska, G.; Minko, S.; Jehnichen, D.; Simon,|P.; Fokin, A. A.; Stamm, M. One-dimensional aggregation of regioregular polyalkylthiophenes. Nano Letters 2003, 3, 707–712.

57.  Gunchenko, P. A.; Vigovskaya, T. S.; Fokin, A. A.; Yurchenko, A. G. A New method for building of [3.3.3]propellan skeleton.  Ukr. Khim. Zhurn. 2003, 69, 10, 113–115.

56.  Fokin, A. A.; Schreiner, P. R. Metal-free, selective alkane functionalizations.  Adv. Chem. Cat. 2003, 345, 1035–1052.

55.  de Meijere, A.; Kozhushkov, S. I.; Fokin, A. A.; Emme, I.; Redlich, S.; Schreiner, P. R. New structurally interesting cyclopropane derivatives. A world of wonders and surprises. Pure Appl. Chem. 2003, 75, 549–562.

54.  Fokin, A. A.; Schreiner, P. R.; Kozhushkov, S. I.; Sattelmeyer, K. W.; Schaefer, H. F.; de Meijere, A. Delocalizations in s-radical cations: The Intriguing structures of ionized [n]rotanes.  Org. Lett. 2003, 5, 697–700.

53.  Tkachenko, B. A.; Shubina, T. E.; Gusev, D. V.; Gunchenko, P. A.; Yurchenko, A. G.; Schreiner, P. R.; Fokin, A. A. Mechanisms of C–H Activation of Alkanes by Chromium-oxo Reagents.  Theoret. and Experim. Khim. 2003, 39, 2, 90–95.

52.   Krasutsky, P. A.; Kolomitsyn, I. V.; Botov, E. M.; Carlson, R. M.; Semenova, I. G.; Fokin, A. A. Heterolytic decarboxylation involving acyltrifluoroacetyl peroxide intermediates. Tetrahedron Lett. 2002, 43, 8687–8691.

51.  Schreiner, P. R.; Fokin, A. A.; Lauenstein, O.;  Okamoto, Y.; Wakita, T.; Rinderspacher, C; Robinson, G. H.; Vohs, J. K.; Campana.; C. F. Pseudotetrahedral polyhaloadamantanes as chirality probes: Synthesis, separation, and absolute configuration.  J. Am. Chem. Soc. 2002, 124, 13348–13349.

50.  Fokin, A. A.; Tkachenko, B. A.; Shubina, T. E.; Gunchenko, P. A.; Gusev, D. V.; Vohs, J. K.; Robinson, R. H.; Yurchenko, A. G.; Schreiner, P. R. The protoadamantane radical cation.  Eur. J. Org. Chem. 2002, 3844–3849.

49.  Shubina, T. E.; Gunchenko, P. A.; Vigovskaya, T. S.; Schreiner, P. R.; Yurchenko, A. G.; Fokin, A. A.  [3.3.2]- and [3.3.3]propellanes in reactions with oxidizing electrophiles. Teoret. i Experim. Khimiya, 2002, 38, 4, 226–231.

46.  Kiriy, A. V.; Yurchenko, A. G.; Fokin, A. A. The new [2,3]-sigmatropic rearrangement of allylsulfinyl carbanions. Russ. J. Org. Chem. 2002, 38, 3, 471–472.

48.  Fokin, A. A.; Shubina, T. E.; Gunchenko, P. A.; Isaev, S. D.; Yurchenko, A. G.; Schreiner, P. R. H-Coupled electron transfer in alkane C–H activations with halogen electrophiles. J. Am. Chem. Soc. 2002, 124, 10718–10727.

47.  Fokin, A. A.; Schreiner, P. R. Selective alkane transformations via radicals and radical cations: Insights into the activation step from experiment and theory. Chem. Rev. 2002, 102, 1551–1593.

45.  Shubina, T. E.; Gunchenko. P. A.; Yurchenko, A. G.; Schreiner, P. R.; Butova, E. D.; Fokin, A. A. Structure and transformations of 1-alkyladamantane radical cations.  Teoret. i Experim. Khimiya 2002, 38, 1, 8–13.

44.  Schreiner, P. R.; Lauenstein, O.; Butova, E. D.; Gunchenko, P. V.; Kolomitsin, I. V.; Wittkopp, A.; Feder, G.; Fokin, A. A. Selective radical reactions in multiphase systems: Phase-transfer halogenations of alkanes. Chem. Eur. J. 2001, 7, 23, 4996–5003.

43.  Fokin, A. A.; Tkachenko, B. A.; Korshunov, O. I.; Gunchenko, P. A.; Schreiner, P. R. Molecule-induced alkane homolysis with dioxiranes. J. Am. Chem. Soc. 2001, 123, 11248–11252.

42.  Prall, M.; Wittkopp, A.; Fokin, A. A.; Schreiner, P. R.  Substituent effects on the Bergman Cyclization of (Z)-1,5-hexadiyne-3-enes: A systematic computational study. J. Comp. Chem. 2001, 22, 13, 1605–1614.

41.  Fornarini, S.; Crestone, E.; Fokin, A. A. The protonation of gaseous cyclopropane. Chem. Eur. J. 2001, 7, 2916–2921.

40.  Schreiner, P. R.; Gunchenko, P. A.; Wittkopp, A.; Yaroshinsky, A. I.; Peleshanko, S. A.; Fokin, A. A.  The rearrangement of the cubane radical cation in solution. Chem. Eur. J. 2001, 7, 2739–2744.

39.  Krasutsky, P. A.; Kolomitsyn, I. V.;  Kiprof, P.;  Carlson, R. M.;  Sydorenko, N. A.; Fokin, A. A.  A Consecutive double-Criegee rearrangement using TFPAA: Stepwise conversion of homoadamantane to oxahomoadamantanes.  J. Org. Chem. 2001, 66, 1701–1707.

38.  Fokin, A. A.; Lauenstein, O.; Gunchenko, P. A.; Schreiner, P. R.  Halogenation of cubane under phase-transfer conditions: Single and double C–H-bond substitution with conservation of the cage Structure.  J. Am. Chem. Soc.  2001, 123, 1842–1847.

37.  Fokin, A. A.; Peleshanko, S. A.; Gunchenko, P. A.; Gusev, D. V.; Schreiner, P. R. Hydrocarbon activations with cerium (IV) ammonium nitrate: Free radical versus oxidative pathways. Eur. J. Org. Chem. 2000, 3357–3362.

36.  Lauenstein, O.; Fokin, A. A.; Schreiner, P. R. A combined experimental and computational study of the H/D kinetic isotope effects for bromination and iodination of aliphatic hydrocarbons under phase-transfer conditions. Org. Lett.  2000, 2201–2204.

35.  Fokin,A. A.;Schreiner,P. R.; Gunchenko, P. A.; Peleshanko, S. A.; Shubina,T. E.; Isaev, S. D.; Tarasenko, P. V.; Kulik, N. I.; Schiebel, H.-M.; YurchenkoA. G. Oxidative single electron transfer activation of s-bonds in aliphatic halogenation reactions. J. Am. Chem. Soc. 2000, 122, 7317–7326.

34.  Fokin, A. A.; Kushko, A. O.; Kirij, A. V.; Yurchenko, A. G.; Schleyer, P. v. R. Direct transformations of ketones to g-unsaturated thiols via [2,3]-sigmatropic rearrangement of allyl sulfinyl carbanions: Combined experimental and theoretical study. J. Org. Chem. 2000, 65, 2984–2995.

33.  Kolomitsin, I. V.; Krasutsky, P. A.; Sidorenko, N. V.; Yurchenko, A. G.; Fokin, A. A.  Oxidative fragmentation of tetrahydrocyclopentadiene structure. Russ. J. Org. Chem. 2000,  36, 456–457.

32.  Krasutsky, P. A.; Kolomitsin, I. V.; Kiprof, P.; Carlson, R. M.; Fokin, A. A. Observation of a stable carbocation in a consecutive Criegee rearrangement with trifluoroperacetic acid. J. Org. Chem. 2000, 65, 3926–3933.

31.  Fokin, A.A.; Kiran, B.; Bremer, M.; Yang, X.; Jiao, H.; Schleyer, P. v. R.  Which electron count rules are needed for four-centered tree-dimensional aromaticity? Chem. Eur. J.; 2000, 6, 1615–1628.

30.  Schreiner, P. R.; Lauenstein, O.; Butova, E. D.; Fokin, A. A. The first efficient iodination of unactivated, aliphatic hydrocarbons. Angew. Chem. 1999, 111 2956–2958. Angew. Chem. Int. Ed. Engl. 1999, 38, 2786–2788. This work is featured: cover picture of the Angewandte Chemie, 1999, issue 18. Chemical and Engineering News 1999 September, 20, 44. Sueddeutsche Zeitung 1999 55, October, 12, p. V2/12.

29.  Fokin, A. A.; Gunchenko, P. A.; Peleshanko, S. A.; Schleyer, P. v. R.; Schreiner, P. R. Common radical cation intermediates in cage hydrocarbon activations.  Eur. J. Org. Chem. 1999, 855–860.

28.  Kushko, A. O.; Yurchenko, A. G.; Kirij, A. V.; Likhotvorik, I. R.; Fokin, A. A.  The novel one-step method of homoallylic tiols synthesis from ketons. Russ. J. Org. Chem. 1998, 34, 776–777.

27.  Fokin, A. A.; Schreiner, P. R.; Schleyer, P. v. R.; Gunchenko, P. A. Electrophilic and oxidative activation of the central C–C Bond in [3.3.n]Propellanes: A theoretical study. J. Org. Chem. 1998,No19, 6494–6502.

26.  Fokin, A. A.; Jiao, H.; Schleyer, P. v. R. From Dodecaheptapentaene to the “[n]Trannulenes”. A new In-plane aromatic family.  J. Am. Chem. Soc. 1998, 120, 9364–9365.

25.  Schreiner, P. R.; Lauenstein, O.; Kolomitsin, I. V.; Fokin, A. A.  Selective C–H activation of aliphatic hydrocarbon under phase-transfer conditions.  Angew. Chem.; Int. Ed. 1998, 37, 1895–1897. This paper was featured in Nachr. Chem. Tech. Lab. 1998 7/8, 706. Chemical and Engineering News 1998 July, 13, 55.

24.  Fokin, A. A.; Gunchenko, P. A.; Tkachenko, B. A.; Butova, E. D.; Yurchenko, A. G.  Backside activation of s-bonds with Cr(VI)-reagents.  Tetrahedron Lett. 1997, 38, 639–642.

23.  Fokin, A. A.; Gunchenko, P. A.; Kulik, N. I.; Iksanova, S. V.; Krasutsky, P. A.; Gogoman, I. V.; Yurchenko, A. G.  NO2+-containing reagents in the electrophilic and oxidative addition to propellanic C–C bond.  Tetrahedron 1996, 52, 5857–5866.

22.  Fokin, A. A.; Gunchenko, P. A.; Krasutsky, P. A.; Yaroshinsky, A. I.; Yurchenko, A. G. Oxidation of tetracyclo[4.3.1.1.4,801,4]undecane (1,4-cyclohomoadamantane). Russ. J. Org. Chem. 1995, 31, 796–797.

21.  Fokin, A. A.; Gunchenko, P. A.; Krasutsky, P. A.; Yaroshinsky, A. I.; Yurchenko, A. G. Oxidative addition to 3,6-dehydrohomoadamantane.  Tetrahedron Lett. 1995, 36, 4479–4482.

20.  Fokin, A. A.; Gagaeva, E. A.; Krasutsky, P. A.; Yurchenko, A. G. Stereoselective epoxidation of 4,7,7-trimethyl-3-oxabicyclo[3.3.1]hept-4-en-2-one. Russ. J. Org. Chem. 1994, 30, 940–941.

19.  Fokin, A. A.; Butova, E. D.; Kolomitsin, I. V.; Gagaeva, E. A.; Kornilov, A. M.; Sorochinsky A. E. Functional derivatives of 2-carene in cyclopropane-containing pyrethroides synthesis. Russ. J. Org. Chem. 1994, 30, 669–679.

18.  Fokin, A. A.; Butova, E. D.; Gulevitch, A. V.; Yurchenko, A. G.; Krasutsky, P. A.  Novel oxidative transformations in norpinonic acid synthesis. Russ. J. Org. Chem. 1993, 29, 1075–1076.

17.  Lichotvorik, I. R.; Litvin, A. L.; Shimko, R. I.; Fokin, A. A. The insertion of dichlorocarbene into tricyclo[5.2.1.02,5]decane structure. Vest. Kiev Polytech. Inst. 1992, 29, 3.

16.  Fokin, A. A.; Krasutsky, P. A.; Gulevich, A.V.; Yurchenko, A. G.  Oxidation of 3,7,7-trimethyl-3,4-dihydroxybicyclo[4.1.0]heptane by molecular oxygen. Russ. J. Org. Chem. 1992, 28, 1098–1099.

15.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structures of 1R-cis-polyhalogenchrysanthemic acids. Russ. J. Org. Chem. 1992, 28, 67–75.

14.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G.  Key synthones of pyrethrinoides based on 3-carene.  Ukr. Khim. Zhurnal 1992, 58, 1130–1135.

13.  Fokin, A. A.; Fedorenko, T. V.; Yurchenko, A. G. Enantioselective synthesis of chrysanthemic acid and derivatives. Ukr. Khim. Zhurnal 1992, 58, 1120–1126.

12.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structure of the stereoisomeric monochlorochrysanthemic acids. Russ. J. Org. Chem. 1991, 27, 1279–1283.

11.  Fokin, A. A.; Krasutsky, P. A.; Baula, O. P.; Yurchenko, A. G.  Functionalization of 4,7,7-trimethyl-3-oxabicyclo[3.31]hept-4-en-2-one with dichlorocarbene. Russ. J. Org. Chem. 1991, 27, 1363.

10.  Krasutsky, P. A.; Fokin, A. A.; Rodionov, V. N.; Kulik, N. I.; Ambrosienko, N. V.; Yurchenko, A. G.  On the mechanisms of transannular acidic cyclization of 3,7-dimethylenobicyclo[3.3.1]nonane and derivatives. Russ. J. Org. Chem. 1991, 27, 992–999.

9.      Krasutsky, P. A.; Fokin, A. A.; Butova, E. D.; Yurchenko, A. G. Stereoselective synthesis of (–)-pirocine and 1R-E-chrysanthemic acid from 2-pinene. Vest. Kiev. Polytech. Inst. 1991, 28, 40–44.

8.      Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G. The structures of carbenilation products of 2-pinene and 3-carene with carboethoxycarbene. Ukr. Khim. Zhurnal 1989, 55,  842–845.

7.      Krasutsky, P. A.; Fokin, A. A.; Maleev, A. V.; Kurkutova, E. N.; Struchkov, Y. T.; Yurchenko, A. G. The structure of adducts of allenes of bicyclo[3.3.1]nonane series with dihalocarbenes. Russ. J. Org. Chem. 1990, 26, 1016–1024.

6.      Krasutsky, P. A.; Fokin, A. A.; Skoba, E. D.; Yurchenko, A. G. the synthesis and protic cyclization of 3-vinylidenobicyclo[3.3.1]nonane-7-one. Russ. J. Org. Chem. 1986, 22, 460–461.

5.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and protic cyclization of 3-vinylideno-7-propadienilidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1986, 22, 459–460.

4.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and reactivity of 3-methylene-7-vinylidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1985, 21, 2522–2626.

3.      Krasutsky, P. A.; Fokin, A. A.; Kulik, N. I.; Yurchenko, A. G. The reactivity of 3,7-divinylidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1985, 21, 2518–2522.

2.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G.; Chekmenyova, L. A. The synthesis of 3,7-divinylidenbicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1984, 20, 1807–1808.

1.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G.; Jones, M. Jr.; Antipin, M. Y.; Struchkov, Y. T. The structure of carbenylation products of 3-methylenebicyclo[3.3.1]nonane. Teoret. i Experim. Khimiya 1984, 20, 427–433.

 

159. Becker, J.; Zhyhadlo, Y. Y.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Ferster, M.; Holthausen, M. C.; Specht, P.; Schindler, S.  Aerobic aliphatic hydroxylation reactions by copper complexes: A simple clipandcleave concept. Chem. Eur. J.2018, 24, https://doi.org/10.1002/chem.201802607

158.Gebbie, M. A.; Ishiwata, H.;  McQuade P.J.; Petrak, V.: Taylor, A.; Freiwald, C.; Dahl, J. E.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Nesladek, M.; Melosh, N. A. Experimental measurement of the diamond nucleation landscape reveals classical and nonclassical features. PNAS, 2018, 115, 33, 8284–8289.

157. Moncea, O.; Poinsot, D.; Fokin, A. A.; Schreiner, P. R.; Hierso, J. C. Palladium-catalyzed C2-H arylation of unprotected (N-H)-indoles “On water” using primary diamantyl phosphine oxides as a class of primary phosphine oxide ligands. ChemCatChem, 2018, 10, 2915 – 2922.

155.Hoc, N. T.  Fokin, A. A; Rodionov, V. N. Towards 3-(2-adamantylidene)diamantane derivatives through the McMurry cross coupling reaction. Org. Commun. 2018, 11, 2x, 75-79.

156. Hoc, N. T.  Fokin, A. A; Rodionov, V. N. Synthesis of 10-methoxydiamantan-3-one. MOLBANK. 2018, 2, UNSP M990. DOI: 10.3390/M990

154.Yan, H.;Narasimha, K. T.; Denlinger, J.;Li, F. H.;Mo, S.-K.;Nathan Hohman, J.;  Dahl, J. E. P.; ,Carlson, R. M. K.;Tkachenko, B. A.;Fokin, A. A.; Schreiner, P. R.; Hussain, Z.; Shen, Z.-X.; ,Melosh, N. A.Monochromatic photocathodes from graphene-stabilized diamondoids. Nano Lett., 2018, 18, 1099–1103.

153.Yan, H.; Yang, F.; Pan, D.; Lin, Y.; Hohman, J. N.; Solis-Ibarra, D.; Li, F. H.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Galli, G.; Mao, W. L.; Shen Z.-X.; Melosh, N. M. Sterically controlled mechanochemistry under hydrostatic pressure. Nature 2018, 554, 505–510.

152.Gunawan, M. A.; Moncea, O.; Poinsot, D.; Keskes, M.; Domenichini, B.; Heintz, O.; Chassagnon, R.; Herbst, F.; Carlson, R. M. K.; Dahl, J. E. P.; Fokin, A. A.; Schreiner, P. R.; Hierso,  J.-C. Nanodiamond-Palladium Core–Shell Organohybrid Synthesis: A Mild Vapor-Phase Procedure Enabling Nanolayering Metal onto Functionalized sp3-Carbon. Adv. Funct. Mater. 2018, 1705786 (15 p).

151.Gunchenko, P. A.; Li,J.; Liu, B.; Chen, H.; Pashenko, A. P.;Bakhonsky, V. V.; Zhuk. T. S.; Fokin, A. A. Aerobic oxidations with N-hydroxyphthalimide in trifluoroacetic acid. Molec. Cat. 2018, 446, 72-79.

150.Zhyhadlo, Y. Y.; Gaidai, A. V.; Sharapa, D. I.; Mitlenko, A. G.; Shishkin, O. V.; Shishkina, S. V.; Levandovskiy, I. A.; Fokin, A. A. Functionalised Cookson's diketones in chlorosulfonic acid: Towards polysubstituted D3-trishomocubanes. J. Chem. Res. 2017, 41, 12, 677-733.

149.Tyborski, C.; Gillen, R.; Fokin, A. A.; Koso, T. V.; Fokina, N. A.; Hausmann, H.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. Electronic and Vibrational Properties of Diamondoid Oligomers. J. Phys. Chem. 2017, 121, 48, 27082–27088

148.     Fokin, A. A.: Zhuk, T. S.; Blomeyer, S.; Peŕez, C.;  Chernish, L.V.; Pashenko, A. E.; Antony, J.; Vishnevskiy, Y. V.;  Berger, R. J. F.; Grimme, S.; Logemann, C.; Schnell, M.; Mitzel N. W.; Schreiner P. R. Intramolecular London dispersion interaction effects on gas-phase and solid-state structures of diamondoid dimers. J. Amer. Chem. Soc. 2017, 139, 16696-16707.

147.     Tyborski, C.; Meinke, R.; Gillen, R.; Bischoff, T.; Knecht, A.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N. Schreiner, P. R.; Moller, T.; Rander, T.; Thomsen, C.; Maultzsch, J. From isolated diamondoids to a van-der-Waals crystal: A theoretical and experimental analysis of a trishomocubane and a diamantane dimer in the gas and solid phase. J. Chem. Phys. 2017, 147, 4, 044303 (6 p.)

146.     Fokin, A. A.; Pashenko, A. E.; Bakhonsky, V. V.; Zhuk. T. S.; Chernish. L. V.; Gunchenko, P. A.; Kushko, A. O.; Becker, J.; Wende, R. C.; Schreiner. P. R. Chiral building blocks based on 1,2-disubstituted diamantanes. Synthesis, 2017. 49, 20032008.

145.     Yan, H.; Hohman, J. N.; Li, F. H.; Jia, C.; Solis-Ibarra, D.; Wu, B.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Vailionis, A.; Kim, T. R.; Devereaux, T. P.; Shen, Z.-X.; Melosh. N. A. Hybrid metal–organic chalcogenide nanowires with electrically conductive inorganic core through diamondoid-directed assembly. Nat. Mater. 2017, 16, 349–355.

144.  Hoc, N. T.;Kushko, A. O.;Fokin, A. A.;Rodionov, V. N. Functional derivatives of diamantanone. Russ. J. Org. Chem. 2016, 52, 8, 1209–1211.

143.Moncea O.; Gunawan, M. A.; Poinsot,D.; Cattey. H.;Becker,J.;Yurchenko,R. I.; Butova,E. D.; Hausmann,H.; Šekutor,M.; Fokin, A. A.; Hierso,J.-C.; Schreiner, P. R. Defying stereotypes with nanodiamonds: Stable primary diamondoid phosphines,  J. Org. Chem. 2016, 81, 8759−8769.

142.     Tverdiy, D. O. Chekanov, M. O.; Savitskiy, P. V.; Syniugin, A. R.; Yarmoliuk, S. M. Fokin, A. A. Efficient preparation of imidazo[1,5-a]pyridine-1-carboxylic acids. Synthesis 2016, 48, A–I.

141.     Ponomarenko, M. V.; Grabowsky,S.; Pal,R.; Röschenthaler, G.-V., Fokin, A. A. SF5-Enolates in Ti(IV)-mediated aldol reactions. J. Org. Chem. 2016, 81, 6783−6791.

140.     Karthik, T. N.; Ge,C.; Fabbri,J. D.; Clay,W.; Tkachenko, B. A.; Fokin, A.A.; Schreiner, P. R.; Dahl, J. E.; Carlson, R. M. K.; Shen, Z. X.; Melosh, N. A. Ultra-low effective work function surfaces using diamondoid monolayers. Nature Nanotech. 2016, 11, 267–273.

139.     Zhang, J. L.; Ishiwata, H.; Babinec, T. M.; Radulaski, M.; Müller, K.; Lagoudakis, K. G.; Dory, C.; Dahl, J.; Edgington, R.; Soulière, V.; Ferro, G.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N.; Vuckovic, J. Hybrid group IV nanophotonic structures incorporating diamond silicon-vacancy color centers. Nano Lett. 2016, 16, 212−217.

138.Syniugin, A. R.; Chekanov, M. O.; Savitskiy, P. V.; Pashenko, A. E.; Zhuk, T. S.; Yarmoluk, S. M.; Fokin, A A. New method for the synthesis of pyrrolo[2,3-b]dihydroquinolines. Tetrahedron Lett.  2016, 57, 213–215.

137.Valentin, L.; Henss, A.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Becker, S.; Würtele, C.; Schindler, S. Transition metal complexes with cage-opened diamondoid tetracyclo[7.3.1.14,12.02,7]tetradeca-6.11-diene. J. Coor. Chem. 2015, 68, 3295–3301.

136.Lourie, L. F.; Serguchev, Yu. A.; Bentya, A. V.; Ponomarenko, M. V.; Rusanov, E. B.; Vovk, M. V.; Fokin, A. A.; Ignat’ev, N. V. Metal free electrophilic fluoro-cyclization of unsaturated N-hydroxy- and N-acetoxyamides with N–F reagents. J. Fluor. Chem. 2015, 179, 42–47.

135.Bremer, M.; Untenecker, H.; Gunchenko, P. A.; Fokin, A. A.; Schreiner P. R.  Inverted carbon geometries: Challenges to experiment and theory. J. Org. Chem. 2015, 80, 6520−6524.

134.     Zhuk, T. S.; Koso, T.; Pashenko, A. E.; Hoc, N. T.; Rodionov, V. N.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Toward an understanding of diamond sp2-defects with unsaturated diamondoid oligomer model. J. Am. Chem. Soc. 2015, 137, 6577−6586.

133.     Gunawan, M. A.; Poinsot, D.; Domenichini, B.; Dirand, C.; Chevalier, S.; Fokin, A. A.; Schreiner, P. R.; Hierso, J.-P. The functionalization of nanodiamonds (diamondoids) as a key parameter of their easily controlled self-assembly in micro- and nanocrystals from the vapor phase. Nanoscale, 2015, 7, 1956–1962.

132.     Barabash, A. V.; Didukh, N. A.; Kibal’nyi, N. A.; Butova, E. D.; Schreiner, P. R.;Fokin, A. A. Unusual aerobic oxidation of sterically hindered 1-diamanty methyl ketone. Russ. J. Org. Chem. 2014, 50, 1690–1691.

131.       Gunchenko, P. A.; Novikovskii, A. A.; Byk, M. V.; Fokin, A. A.  Structure and transformations of diamantane radical cation: Theory and experiment. Russ. J. Org. Chem. 2014, 50, 1749–1754.

130.Mishura, A. M.; Sklyarova, A. S.; Shamota, T. V.: Rodionov, V. N.; Fokin, A. A.  Preparative synthesis of pentacyclo[6.3.0.02,6.03,10.05,9]undecan-4-one (D3-Trishomocubanone). Russ. J. Org. Chem. 2014, 50, 1542–1544.

129.Barabash, A. V.; Butova, E. D.; Kanyuk, I. M.; Schreiner, P. R.; Fokin, A. A. Beyond the Corey reaction II: Dimethylenation of sterically congested ketones J. Org. Chem. 2014, 79, 10669−10673. ACS Editor’s Choice, 01.10.2014.

128.Randel, J. C.; Niestemski, F. C.; Botello-Mendez, A. R.; Mar, W.; Ndabashimiye, G.; Melinte, S.; Dahl, J. E. P.; Carlson R. M. K.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Charlier, J.-C.; Manoharan, H. C. Unconventional molecule-resolved current rectification in diamondoid fullerene hybrids. Nature Comm. 2014, 5, 4877 (6 p).

127.Tchernobaev, I. I.; Serguchev, Yu. A.; Fokin, A. A. Mechanism and selectivities of the chlorination of toluene in the presence of catalytical composition antimony pentachloride – benzodithio crown ether. Ukr. Krim. Zhurn. 2014, 50, 45–49.

126.Ponomarenko, M. V.; Serguchev, Yu. A.; Hirschberg, M. E.; Röschenthaler, G.-V.; Fokin, A. A. Elemental F2 with transannular dienes: Regioselectivities and mechanisms. Chem. Eur. J. 2014, 20, 10383–10391.

125.Fokin, A.A.; Yurchenko, R. I.; Tkachenko,B.A.; Fokina,N. A.; Gunawan,M. A.; Poinsot,D.; Dahl, J. E. P.; Carlson,R. M. K.; Serafin,M.; Cattey,H.; Hierso,J.-C.; Schreiner, P. R. Selective preparation of diamondoid phosphonates. J. Org. Chem. 2014, 79, 5369–5373.

124.Fokin, A. A.; Zhuk, T. S.; Pashenko, A. E.; Osipov, V. V.; Gunchenko,P. A.; Serafin, M.; Schreiner, P. R. Functionalization of homodiamantane: Oxygen insertion reactions without rearrangement with dimethyldioxirane. J. Org. Chem. 2014, 79, 1861–1866.

123.Meinke, R.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. UV resonance Raman analysis of trishomocubane and diamondoid dimers. J. Chem. Phys. 2014, 140, 034309 (5p).

122.Kahl, P.; Tkachenko, B. A.; Novikovsky, A. A.; Backer, J.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.  Efficient peparation of aically substituted damondoid drivatives, Synthesis 2014, 46, 787–798.

121.Gunawan, M. A.; Hierso, J.-C.; Poinsot, D.; Fokin, A. A.; Fokina, N. A.; Tkachenko, B. A.;Schreiner, P. R. Diamondoids: Functionalization and subsequent applications of perfectly defined molecular cage hydrocarbons. New J. Chem. 2014, 38, 28–41.

120.     Chekanov, M. O.; Ostrynska, O. V.; Tarnavskyi, S. S.; Synyugin, A. R.; Briukhovetska, N. V.; Bdzhola, V. G.; Pashenko, A. E.; Fokin A. A.; Yarmoluk, S. M. Design, synthesis and biological evaluation of 2-aminopyrimidinones and their 6-aza-analogs as a new class of СК2 inhibitors. J. Enz. Inhib. Med. Chem. 2014, 29, 5, 639­–646.

119.     Ponomarenko, M. V.; Lummer, K.; Fokin, A. A.; Serguchev, Yu. A.; Bassil,B. S.; Röschenthaler, G.-V.  Preparations of SF5- and CF3-substituted arenes utilizing the 7-oxabicyclo­[2.2.1]hept-2-ene synthones. Org. Biomol. Chem. 2013, 11, 8103­–8112.

118.     Kacharov, A. D.; Yemets, S. V.; Nemykin,V. N.; Kacharova, L. M.; Fokin,A. A.; Krasutsky, P. A. Stereoselectivity of A-ring contraction for 3-oxotriterpenoids.  RCS Advances 2013, 3, 19057–19063.

117.     Mishura,A. M.; Sklyarova,A. S.; Sharapa, D. I.; Levandovsky, I. A.; Serafin, M.; Fokin, A. A.; Rodionov, V. N. Stereoselective Preparation of mono- and bis-derivatives of pentacyclo[6.3.0.02,6.03,10.05,9]undecane (D3-trishomocubane). Open. Chem.  2013, 11, 2144–2150.

116.Li, F. H.; Fabbri, J. D.; Yurchenko, R. I.; Mileshkin, A. N.; Hohman, J. N.; Yan, H.; Yuan, H.; Tran, I. C.; Willey, T. M.; Bagge-Hansen, M.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N. A. Covalent attachment of diamondoid phosphonic acid dichlorides to tungsten oxide surfaces. Langmuir 2013, 29, 9790–9797.

115.Zimmermann, T.; Richter, R.; Knecht, A.; Fokin, A. A.; Koso, T. V.; Chernish, L. V.; Gunchenko, P. A.; Schreiner, P. R.; Moller, T.; Rander, T. Exploring covalently bound diamondoid aggregates with valence photoelectron spectroscopy. J. Chem. Phys. 2013, 139, 084310 (6 p).

114.Fokin, A. A.; Butova, E. D.; Barabash, A. V; Huu, N. N.; Tkachenko. B. A.; Fokina, N. A.; Schreiner, P. R. Preparative synthesis of vinyl diamondoids. Synth. Comm. 2013, 43, 1772–1777.

113.Sklyarova, A. S.; Rodionov, V. N.; Parsons, C. G.; Quack, G.; Schreiner, P. R.; Fokin, A. A. Preparation and testing of homocubyl amines as therapeutic NMDA receptor antagonists. Med. Chem. Res. 2013, 22, 360–366.

112.     Clay, W. A.; Maldonado, J. R.;  Pianetta, P.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Melosh, N.; Shen, Z.-X. Photocathode device using diamondoid and cesium bromide films Appl. Phys. Lett. 2012, 101, 241605 (5p).

111.Ishiwata, H.; Acremann, Y.; Scholl, A.; Rotenberg, E.; Hellwig, O.; Dobisz, E.; Doran, A.; Tkachenko, B.A.; Fokin, A.A.; Schreiner, P.R.; Dahl, J.E.P.; Carlson, R.M.K.; Melosh, N.; Shen, Z.-X.; Oldag, H. Diamondoid coating enables disruptive approach for chemical and magnetic imaging with 10 nm spatial resolution. Appl. Phys. Lett. 2012, 101, 163101 (5 p).

110.Fokin, A. A.;  Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Hausmann, H.; Serafin, M.; Dahl J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Stable alkanes containing very long carbon–carbon bonds. J. Am. Chem. Soc. 2012, 134, 1364113650.

109.     Gunchenko, P. A.; Fokin, A. A. Mechanisms of activation of C–H bonds in framework compounds: Theory and experiment. Theoret. Experim. Khim. 2012, 47, 6, 343–360.

108.     Gaidai, A. V.; Volochnyuk, D. M.; Shishkin, O. V.; Fokin, A. A.; Levandovskiy, I. A.; Shubina, T. E. D3-Trishomocubane-4-carboxylic acid as a new chiral building block: Synthesis and absolute configuration. T. E. Synthesis 2012, 44, 810–816.ю

107.Fokina, N. A.; Tkachenko, B. A.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner P. R.  Synthesis of diamondoid carboxylic acid. Synthesis 2012, 44, 259–264.1

106.Fokin, A. A.; Gerbig, D.; Schreiner, P. R. σ/σ- and π/π-Interactions are equally important: multilayered graphanes. J. Am. Chem. Soc. 2011, 133, 20036–20039.

105.Rodionov, V. N.; Sklyarova, A. S.; Shamota, T. V.; Schreiner, P. R.; Fokin, A. A. Selective reductive dimerization of homocubane series oximes. Russ. J. Org. Chem. 2011, 47, 11, 1695−1702.

104.     Schreiner, P. R.; Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Hausmann, H.; Serafin, M.; Schlecht, S.; Dahl J. E. P.; Carlson, R. M. K.; Fokin, A. A. Overcoming  lability of extremely long alkane carbon–carbon bonds through dispersion forces. Nature 2011, 477, 308–311. This paper was featured in Chemical & Engineering News, 89(38), September 19, 2011 [Science & Technology, Concentrates]

103.Novikovskii, A. A.; Gunchenko P. A.; Prikhodchenko P. G.; Serguchev, Yu. A.; Schreiner P. R.; Fokin A.A. Comparative theoretical and experimental analysis of hydrocarbon σ-radical cations. Russ. J. Org. Chem. 2011, 47, 1293–1299.

102.     Shubina, T. E.; Fokin, A. A. Hydrocarbon s-radical cations. WIREs Comput. Mol. Sci. 2011, 1 661679.

101.     Serguchev, Yu. A.; Ponomarenko, M. V.; Lourie, L. F.; Fokin, A. A. Transannular additions of selectfluor and xenon difluoride: regioselectivity and mechanism. J. Phys. Org. Chem. 2011, 24, 407–413.

100.     Butova, E. D.; Barabash, A. V.; Petrova, A. A.; Kleiner, C. M.; Schreiner, P. R.; Fokin. A. A. Stereospecific consecutive epoxide ring expansion with dimethylsulfoxonium methylide, J. Org. Chem. 2010, 75, 18, 6229–6235.

99.    Demchenko, P. Yu.; Gladyshevskii, R. E.; Volkov, S. V.; Kharkova, L. B.; Yanko, O. G.; Fokina, Z. A.; Fokin, A. A. The first nonaselenium ring. Chem. Commun. 2010, 46, 4520–4522.

98.  Lysenko, A. B.; Senchyk, G. A.; Lincke, J.; Lässig, D.; Fokin, A. A.; Butova, E. D.; Schreiner, P. R.; Krautscheid, H.; Domasevitch, K. V. Metal oxide-organic frameworks (MOOFs), a new series of coordination hybrids constructed from molybdenum(VI) oxide and bitopic 1,2,4-triazole linkers. Dalton Trans. 2010, 39, 4223–4231.

97.  Zhuk, T. S.; Bratko, E. Y.; Pashenko, A. E.; Gunchenko, P. A.; Yurchenko, A. G.; Schreiner, P. R.; Fokin, A. A. The “green” synthesis of neuroprotecting drug Memantine. J. Org. Pharm. Chem. 2010, 8, 62–66.

96.  Roth, S.; Leuenberger, D.; Osterwalder, J.; Dahl, J. E.; Carlson, R. M. K.; Tkachenko, B. A. Fokin, A. A.; Schreiner, P. R., Hengsberger, M. Negative-electron-affinity diamondoid monolayers as high-brilliance source for ultrashort electron pulses. Chem. Phys. Lett.  2010, 495, 102–108.

95.  Landt, L.; Bostedt, C.; Wolter, D.; Möller, T.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Kulesza, A.; Bonacic-Koutecky, V. Experimental and theoretical studies of the absorption properties of thiolated diamondoids. J. Chem. Phys. 2010, 132, 144305 (6p).

94.  Landt, L.; Staiger, M.; Wolter, D.; Klünder, K.; Zimmermann, P.; Willey, T. M.; van Buuren, T.; Brehmer, D.; Schreiner, P. R.; Tkachenko, B. A.; Fokin, A. A.; Möller, T.; Bostedt, C. The influence of a single thiol group on the electronic and optical properties of the smallest diamondoid adamantane. J. Chem. Phys. 2010, 132, 0247101(7p).

93.  Levandovskiy, I. A.; Shubina, T. E.; Fokin, A. A. Computational and QSAR study of the alkylnaphthyl ketones adsorption on silver-ion stationary phase.  J. Molec. Mod. 2010, 16, 513–522.

92.  Schreiner, P. R.; Fokin, A. A.; Reisenauer, H. P.;  Tkachenko, B. A.; Vass, E.; Olmstead, M. M.; Bläser, D.; Boese, R.; Dahl, J. E. P.; Carlson, R. M. K. [123]Tetramantane: Parent of a new family of σ-helicenes. J. Am. Chem. Soc. 2009, 131, 11292–11293.

91.  Fokin, A. A.; Gunchenko, P. A.; Novikovsky, A. A.; Shubina, T. E.; Chernyaev, B. V.; Dahl J. E. P.; Carlson, R. M. K.; Yurchenko, A. G.; Schreiner P. R. Photoacetylation of diamondoids: Selectivities and mechanism. Eur. J. Org. Chem. 2009, 5153–5161. This work is featured: Cover picture of the Eur. J. Org. Chem., 2009, issue 30.

90.  Fokin, A. A.; Zhuk, T. S.; Pashenko, A. E.; Dral, P. O.; Gunchenko, P. A.;Dahl, J. E. P.;Carlson, R. M. K.;Koso, T. V.;Serafin, M.; Schreiner, P. R. Oxygen-doped nanodiamonds: Synthesis and functionalizations. Org. Lett. 2009, 11, 3068–3071.

89.  Sklyarova, A. S.; Rodionov, V. N.; Fokin, A. A. A convenient preparative synthesis of pentacyclo[5.3.0.02,5.03,9.04,8]decane (C2-bishomocubane). Russ. J. Org. Chem. 2009, 45, 11, 1644−1647.

88.  Gunchenko, P. A.; Makuhina, A. M.; Novikovsky, A. A.; Yurchenko, A. G.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Structure and transformations of homoadamantane radical cation.  Theoret. and Experim. Khim. 2009, 45, 4, 246–251.

87.  Willey, T. M.; Lee, J. R. I.; Fabbri, J. D.; Wang, D.; Nielsen, M. H.; Randel, J. C.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Dahl, J. E. P.; Carlson, R. M. K.; Terminello, L. J.; Melosh, N. A.; van Buuren, T. Determining orientational structure of diamondoid thiols attached to silver using near-edge X-ray absorption fine structure spectroscopy. J. Elec. Spectr. Rel. Phen. 2009, 172, 69–77.

86.  Schwertfeger, H.; Würtele, C.; Hausmann, H.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R. Selective preparation of diamondoid fluorides. Adv. Synth. Catal. 2009, 351, 1041–1054.

85.  Fokin, A. A.; Schreiner, P. R. Band gap tuning in nanodiamonds: First principle computational studies. Molec. Phys. 2009, 107, 8–12, 823–830.

84.  Fokin, A. A.; Tkachenko, B. A.; Fokina, N.  A.; Hausmann, H.; Serafin, M.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Reactivities of the prism-shaped diamondoids [1(2)3]tetramantane and [12312]hexamantane (cyclohexamantane). Chem. Eur. J. 2009, 15, 3851–3862.

83.  Fokin, A. A.; Merz, A.; Fokina, N. A.; Schwertfeger, H.; Liu, S. L.; Dahl, J. E. P.; Carlson, R. K. M.; Schreiner, P. R.  Synthetic routes to aminotriamantanes, topological analogues of the neuroprotector memantine. Synthesis 2009, 909–912.

82.  Clay, W. A.; Liu, Z.; Yang, W.; Fabbri, J. D.; Dahl, J. E.; Carlson, R. M. K.; Sun, Y.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Pianetta, P. A.; Melosh, N.; Shen Z.-X. Origin of the monochromatic photoemission peak in diamondoid monolayers. Nano Lett. 2009, 9, 57–61.

81.  Willey, T. M.; Fabbri, J. D.; Lee, J. R. I.; Schreiner, P. R.; Fokin, A. A.; Fokina, N. A; Dahl, J. E. P.; Carlson, R. M. K.; Vance, A. L.; Yang, W.; Terminello, L. J.; van Buuren, T.; Melosh, N. A.  Near-edge X-ray absorption fine structure spectroscopy of diamondoid thiol monolayers on gold.  J. Am. Chem. Soc. 2008, 130, 10536–10544.

80.  Chernish, L. V.; Gunchenko, P. A.; Barabash, A. B.; Goreslavets, V. S.; Yurchenko, A. G.; Fokin, A. A. Selective synthesis of 1,1-diadamantane monoderivatives.  Zhurn. Org. Pharm. Khim. 2008, 6, 48–51.

79.  Zhuk, T. S.; Gunchenko, P. A.; Korovai, Ya. Yu.; Schreiner,P. R.; Fokin A. A. Mechanisms of the C–H halogenation of adamantane in the presence of N-hydroxyphthalimide.   Theoret. and Experim. Khim.  2008, 44, 1, 46–51.

78.  Schwertfeger, H; Fokin, A. A.; Schreiner, P. R. Diamonds are a chemist’s best friend: Diamondoid chemistry beyond adamantane.  Angew. Chem. Int. Ed. 2008, 47, 1022–1036.

77.  Fokin, A. A.; Yurchenko, A. G.; Rodionov, V. N.; Gunchenko, P. A.; Yurchenko, R. I.; Reichenberg, A.; Wiesner, J.; Hintz, M.; Jomaa, H.; Schreiner, P.R. Synthesis of the antimalarial drug FR900098 utilizing the nitroso-ene reaction. Org. Lett. 2007, 9, 4379–4382. G

76.  Fokina, N. A.; Tkachenko, B. A.; Merz, A.; Serafin, M.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R. Hydroxy derivatives of diamantane, triamantane, and [121]tetramantane: Selective preparation of bis-apical derivatives. Eur. J. Org. Chem. 2007, 4738–4745.

75.  Butova, E. D.; Fokin, A. A.; Schreiner, P. R. Beyond the Corey reaction: One-Step diolefination of cyclic ketones. J. Org. Chem. 2007, 72, 5689–5696.

74.  Fokin, A. A.; Butova, E. D.; Chernish, L. V.; Fokina, N. A.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Simple preparation of diamondoid 1,3-dienes via oxetane ring opening. Org. Lett. 2007, 9, 2541–2544.0

73.  Yang, W. L.; Fabbri J. D.; Willey, T. M.; Lee, J. R. I.; Dahl, J. E.; Carlson, R. M. K.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Meevasana, W.; Mannella, N.; Tanaka, K.; Zhou, X. J.; van Buuren, T.; Kelly, M. A.; Hussain, Z.; Melosh, N. A.; Shen, Z.-X. Monochromatic electronphotoemission from diamondoid monolayers. Science 2007, 316, 1460–1462.

72.       Wodrich, M. D.; Corminboeuf, C.; Schreiner, P. R.; Fokin, A. A.; Schleyer, P. v. R. How accurate are DFT treatments of organic energies? Org. Lett. 2007, 9, 1851–1854.

71.  Schreiner, P. R.; Fokin, A. A.; Pascal, R. A., Jr.; de Meijere, A. Many density functional theory approaches fail to give reliable large hydrocarbon isomer energy differences. Org. Lett. 2006, 8, 3635–3638.

70.  Fokin, A. A.; Schreiner, P. R.; Fokina, N. A.; Tkachenko, B. A.; Hausmann, H.; Serafin, M. Dahl, J. E. P.; Liu, S.; Carlson, R. M. K.  Functionalized nanodiamonds Part 4: Reactivity of [1(2,3)4]pentamantane (Td-Pentamantane): A nanoscale model of diamond J. Org. Chem. 2006, 71, 8532–8540.

69.   Ponomarenko, M. V.; Serguchev Y. A.; Ponomarenko, B. V.; Röschenthaler, G.-V.; Fokin, A. A. Experimental and theoretical studies on the transannular cyclizations of 3,7-dimethylenebicyclo[3.3.1]nonane with polyfluoroalkyl radicals.  J. Fluor. Chem, 2006, 127, 842–849.

68.  Schreiner, P. R.; Fokina, N. A.; Tkachenko, B. A.; Hausmann, H.; Serafin, M.; Dahl, J. E. P.; Liu, S.; Carlson, R. M. K.; Fokin, A. A. Functionalized Nanodiamonds Part 2: Triamantane and [121]Tetramantane. J. Org. Chem. 2006, 71, 18, 6709–6720. This work is featured: Cover picture of the J. Org. Chem., 2006, issue 18.

67.  Tkachenko, B. A.; Fokina, N. A.; Chernish, L. V.; Dahl, J. E. P.; Liu, S.; Carlson, M. K.; Fokin, A. A.; Schreiner, P. R. Functionalized Nanodiamonds Part 3: Thiolation of tertiary/bridgehead alcohols. Org. Lett. 2006, 8, 1767–1770.

66.  Fokin, A. A.; Schreiner, P. R.; Berger, R.; Robinson, G. H.; Wei, P.; Campana, C. F. Pseudotetrahedral polyhalocubanes: Synthesis, structures, and parity violating energy differences. J. Am. Chem. Soc. 2006, 128, 5332–5333. This work is featured: Nature, 2006, 44, 4, 5.

65.  Fokin, A. A.; Tkachenko, B. A.; Gunchenko, P. A. Gusev, D. V. Schreiner, P. R. Functionalized Nanodiamonds Part I. An experimental assessment of diamantane and computational predictions for higher diamondoids. Chem. Eur. J. 2005, 11, 7091–7101.

64.  de Meijere, A.; Lee, C.-H.; Kuznetsov M. A.; Gusev, D. V.; Kozhushkov, S. I.; Fokin, A. A.; Schreiner, P. R. Preparation and reactivity of [D3d]-octahedrane: The most stable (CH)12 hydrocarbon. Chem. Eur. J. 2005, 11, 6175–6184.

63.  Rodionov, V. N.; Chernyaev, B. V.; Levandovskii, I. A.; Shubina, T. E.; Fokin, A. A..  Quantum-chemical interpretation of the reorientation of dialkyl-cis-9,10-dihydroanthracene-9,10-endofumarates on a silver-containing stationary phase.  Theoret. and Experim. Khim. 2005, 41, 1, 1–6.

62.  Rodionov, V. M.; Chernyaev, B. V.; Levandovs'kii, I. A.; Shubina, T. E.; Fokin, A. A.; Yurchenko, O. G.  Experimental and quantum-chemical study of the thermodynamics of complexation of methylbenzenes with silver(I) ion.    Naukovi Visti - Natsional'nii Tekhnichnii Universitet Ukraini "Kiivs'kii Politekhnichnii Institut"  2005, 1, 107–115.

61.  Fokin, A. A.; Tkachenko, B. A.; Gunchenko, P. A.; Schreiner, P. R. The protonation of cubane revisited. Angew. Chem. Int. Ed. 2005, 44, 146–149.

60.  Schreiner, P. R.; Fokin, A. A.; Kotke, M.; Weil, T. Noncovalent organocatalysis.  Ann. Pol. Chem. Soc. 2004, 3, part 1, 21–24.

59.  Schreiner, P. R.; Fokin, A. A. Selective alkane C–H-bond functionalizations utilizing oxidative single-electron transfer and organocatalysis. Chem. Record 2004, 3, 247–257.

58.  Kiriy, N.; Jahne, E.; Adler, H.-J.; Schneider, M.; Kiriy, A.; Gorodyska, G.; Minko, S.; Jehnichen, D.; Simon,|P.; Fokin, A. A.; Stamm, M. One-dimensional aggregation of regioregular polyalkylthiophenes. Nano Letters 2003, 3, 707–712.

57.  Gunchenko, P. A.; Vigovskaya, T. S.; Fokin, A. A.; Yurchenko, A. G. A New method for building of [3.3.3]propellan skeleton.  Ukr. Khim. Zhurn. 2003, 69, 10, 113–115.

56.  Fokin, A. A.; Schreiner, P. R. Metal-free, selective alkane functionalizations.  Adv. Chem. Cat. 2003, 345, 1035–1052.

55.  de Meijere, A.; Kozhushkov, S. I.; Fokin, A. A.; Emme, I.; Redlich, S.; Schreiner, P. R. New structurally interesting cyclopropane derivatives. A world of wonders and surprises. Pure Appl. Chem. 2003, 75, 549–562.

54.  Fokin, A. A.; Schreiner, P. R.; Kozhushkov, S. I.; Sattelmeyer, K. W.; Schaefer, H. F.; de Meijere, A. Delocalizations in s-radical cations: The Intriguing structures of ionized [n]rotanes.  Org. Lett. 2003, 5, 697–700.

53.  Tkachenko, B. A.; Shubina, T. E.; Gusev, D. V.; Gunchenko, P. A.; Yurchenko, A. G.; Schreiner, P. R.; Fokin, A. A. Mechanisms of C–H Activation of Alkanes by Chromium-oxo Reagents.  Theoret. and Experim. Khim. 2003, 39, 2, 90–95.

52.   Krasutsky, P. A.; Kolomitsyn, I. V.; Botov, E. M.; Carlson, R. M.; Semenova, I. G.; Fokin, A. A. Heterolytic decarboxylation involving acyltrifluoroacetyl peroxide intermediates. Tetrahedron Lett. 2002, 43, 8687–8691.

51.  Schreiner, P. R.; Fokin, A. A.; Lauenstein, O.;  Okamoto, Y.; Wakita, T.; Rinderspacher, C; Robinson, G. H.; Vohs, J. K.; Campana.; C. F. Pseudotetrahedral polyhaloadamantanes as chirality probes: Synthesis, separation, and absolute configuration.  J. Am. Chem. Soc. 2002, 124, 13348–13349.

50.  Fokin, A. A.; Tkachenko, B. A.; Shubina, T. E.; Gunchenko, P. A.; Gusev, D. V.; Vohs, J. K.; Robinson, R. H.; Yurchenko, A. G.; Schreiner, P. R. The protoadamantane radical cation.  Eur. J. Org. Chem. 2002, 3844–3849.

49.  Shubina, T. E.; Gunchenko, P. A.; Vigovskaya, T. S.; Schreiner, P. R.; Yurchenko, A. G.; Fokin, A. A.  [3.3.2]- and [3.3.3]propellanes in reactions with oxidizing electrophiles. Teoret. i Experim. Khimiya, 2002, 38, 4, 226–231.

46.  Kiriy, A. V.; Yurchenko, A. G.; Fokin, A. A. The new [2,3]-sigmatropic rearrangement of allylsulfinyl carbanions. Russ. J. Org. Chem. 2002, 38, 3, 471–472.

48.  Fokin, A. A.; Shubina, T. E.; Gunchenko, P. A.; Isaev, S. D.; Yurchenko, A. G.; Schreiner, P. R. H-Coupled electron transfer in alkane C–H activations with halogen electrophiles. J. Am. Chem. Soc. 2002, 124, 10718–10727.

47.  Fokin, A. A.; Schreiner, P. R. Selective alkane transformations via radicals and radical cations: Insights into the activation step from experiment and theory. Chem. Rev. 2002, 102, 1551–1593.

45.  Shubina, T. E.; Gunchenko. P. A.; Yurchenko, A. G.; Schreiner, P. R.; Butova, E. D.; Fokin, A. A. Structure and transformations of 1-alkyladamantane radical cations.  Teoret. i Experim. Khimiya 2002, 38, 1, 8–13.

44.  Schreiner, P. R.; Lauenstein, O.; Butova, E. D.; Gunchenko, P. V.; Kolomitsin, I. V.; Wittkopp, A.; Feder, G.; Fokin, A. A. Selective radical reactions in multiphase systems: Phase-transfer halogenations of alkanes. Chem. Eur. J. 2001, 7, 23, 4996–5003.

43.  Fokin, A. A.; Tkachenko, B. A.; Korshunov, O. I.; Gunchenko, P. A.; Schreiner, P. R. Molecule-induced alkane homolysis with dioxiranes. J. Am. Chem. Soc. 2001, 123, 11248–11252.

42.  Prall, M.; Wittkopp, A.; Fokin, A. A.; Schreiner, P. R.  Substituent effects on the Bergman Cyclization of (Z)-1,5-hexadiyne-3-enes: A systematic computational study. J. Comp. Chem. 2001, 22, 13, 1605–1614.

41.  Fornarini, S.; Crestone, E.; Fokin, A. A. The protonation of gaseous cyclopropane. Chem. Eur. J. 2001, 7, 2916–2921.

40.  Schreiner, P. R.; Gunchenko, P. A.; Wittkopp, A.; Yaroshinsky, A. I.; Peleshanko, S. A.; Fokin, A. A.  The rearrangement of the cubane radical cation in solution. Chem. Eur. J. 2001, 7, 2739–2744.

39.  Krasutsky, P. A.; Kolomitsyn, I. V.;  Kiprof, P.;  Carlson, R. M.;  Sydorenko, N. A.; Fokin, A. A.  A Consecutive double-Criegee rearrangement using TFPAA: Stepwise conversion of homoadamantane to oxahomoadamantanes.  J. Org. Chem. 2001, 66, 1701–1707.

38.  Fokin, A. A.; Lauenstein, O.; Gunchenko, P. A.; Schreiner, P. R.  Halogenation of cubane under phase-transfer conditions: Single and double C–H-bond substitution with conservation of the cage Structure.  J. Am. Chem. Soc.  2001, 123, 1842–1847.

37.  Fokin, A. A.; Peleshanko, S. A.; Gunchenko, P. A.; Gusev, D. V.; Schreiner, P. R. Hydrocarbon activations with cerium (IV) ammonium nitrate: Free radical versus oxidative pathways. Eur. J. Org. Chem. 2000, 3357–3362.

36.  Lauenstein, O.; Fokin, A. A.; Schreiner, P. R. A combined experimental and computational study of the H/D kinetic isotope effects for bromination and iodination of aliphatic hydrocarbons under phase-transfer conditions. Org. Lett.  2000, 2201–2204.

35.  Fokin,A. A.;Schreiner,P. R.; Gunchenko, P. A.; Peleshanko, S. A.; Shubina,T. E.; Isaev, S. D.; Tarasenko, P. V.; Kulik, N. I.; Schiebel, H.-M.; YurchenkoA. G. Oxidative single electron transfer activation of s-bonds in aliphatic halogenation reactions. J. Am. Chem. Soc. 2000, 122, 7317–7326.

34.  Fokin, A. A.; Kushko, A. O.; Kirij, A. V.; Yurchenko, A. G.; Schleyer, P. v. R. Direct transformations of ketones to g-unsaturated thiols via [2,3]-sigmatropic rearrangement of allyl sulfinyl carbanions: Combined experimental and theoretical study. J. Org. Chem. 2000, 65, 2984–2995.

33.  Kolomitsin, I. V.; Krasutsky, P. A.; Sidorenko, N. V.; Yurchenko, A. G.; Fokin, A. A.  Oxidative fragmentation of tetrahydrocyclopentadiene structure. Russ. J. Org. Chem. 2000,  36, 456–457.

32.  Krasutsky, P. A.; Kolomitsin, I. V.; Kiprof, P.; Carlson, R. M.; Fokin, A. A. Observation of a stable carbocation in a consecutive Criegee rearrangement with trifluoroperacetic acid. J. Org. Chem. 2000, 65, 3926–3933.

31.  Fokin, A.A.; Kiran, B.; Bremer, M.; Yang, X.; Jiao, H.; Schleyer, P. v. R.  Which electron count rules are needed for four-centered tree-dimensional aromaticity? Chem. Eur. J.; 2000, 6, 1615–1628.

30.  Schreiner, P. R.; Lauenstein, O.; Butova, E. D.; Fokin, A. A. The first efficient iodination of unactivated, aliphatic hydrocarbons. Angew. Chem. 1999, 111 2956–2958. Angew. Chem. Int. Ed. Engl. 1999, 38, 2786–2788. This work is featured: cover picture of the Angewandte Chemie, 1999, issue 18. Chemical and Engineering News 1999 September, 20, 44. Sueddeutsche Zeitung 1999 55, October, 12, p. V2/12.

29.  Fokin, A. A.; Gunchenko, P. A.; Peleshanko, S. A.; Schleyer, P. v. R.; Schreiner, P. R. Common radical cation intermediates in cage hydrocarbon activations.  Eur. J. Org. Chem. 1999, 855–860.

28.  Kushko, A. O.; Yurchenko, A. G.; Kirij, A. V.; Likhotvorik, I. R.; Fokin, A. A.  The novel one-step method of homoallylic tiols synthesis from ketons. Russ. J. Org. Chem. 1998, 34, 776–777.

27.  Fokin, A. A.; Schreiner, P. R.; Schleyer, P. v. R.; Gunchenko, P. A. Electrophilic and oxidative activation of the central C–C Bond in [3.3.n]Propellanes: A theoretical study. J. Org. Chem. 1998,No19, 6494–6502.

26.  Fokin, A. A.; Jiao, H.; Schleyer, P. v. R. From Dodecaheptapentaene to the “[n]Trannulenes”. A new In-plane aromatic family.  J. Am. Chem. Soc. 1998, 120, 9364–9365.

25.  Schreiner, P. R.; Lauenstein, O.; Kolomitsin, I. V.; Fokin, A. A.  Selective C–H activation of aliphatic hydrocarbon under phase-transfer conditions.  Angew. Chem.; Int. Ed. 1998, 37, 1895–1897. This paper was featured in Nachr. Chem. Tech. Lab. 1998 7/8, 706. Chemical and Engineering News 1998 July, 13, 55.

24.  Fokin, A. A.; Gunchenko, P. A.; Tkachenko, B. A.; Butova, E. D.; Yurchenko, A. G.  Backside activation of s-bonds with Cr(VI)-reagents.  Tetrahedron Lett. 1997, 38, 639–642.

23.  Fokin, A. A.; Gunchenko, P. A.; Kulik, N. I.; Iksanova, S. V.; Krasutsky, P. A.; Gogoman, I. V.; Yurchenko, A. G.  NO2+-containing reagents in the electrophilic and oxidative addition to propellanic C–C bond.  Tetrahedron 1996, 52, 5857–5866.

22.  Fokin, A. A.; Gunchenko, P. A.; Krasutsky, P. A.; Yaroshinsky, A. I.; Yurchenko, A. G. Oxidation of tetracyclo[4.3.1.1.4,801,4]undecane (1,4-cyclohomoadamantane). Russ. J. Org. Chem. 1995, 31, 796–797.

21.  Fokin, A. A.; Gunchenko, P. A.; Krasutsky, P. A.; Yaroshinsky, A. I.; Yurchenko, A. G. Oxidative addition to 3,6-dehydrohomoadamantane.  Tetrahedron Lett. 1995, 36, 4479–4482.

20.  Fokin, A. A.; Gagaeva, E. A.; Krasutsky, P. A.; Yurchenko, A. G. Stereoselective epoxidation of 4,7,7-trimethyl-3-oxabicyclo[3.3.1]hept-4-en-2-one. Russ. J. Org. Chem. 1994, 30, 940–941.

19.  Fokin, A. A.; Butova, E. D.; Kolomitsin, I. V.; Gagaeva, E. A.; Kornilov, A. M.; Sorochinsky A. E. Functional derivatives of 2-carene in cyclopropane-containing pyrethroides synthesis. Russ. J. Org. Chem. 1994, 30, 669–679.

18.  Fokin, A. A.; Butova, E. D.; Gulevitch, A. V.; Yurchenko, A. G.; Krasutsky, P. A.  Novel oxidative transformations in norpinonic acid synthesis. Russ. J. Org. Chem. 1993, 29, 1075–1076.

17.  Lichotvorik, I. R.; Litvin, A. L.; Shimko, R. I.; Fokin, A. A. The insertion of dichlorocarbene into tricyclo[5.2.1.02,5]decane structure. Vest. Kiev Polytech. Inst. 1992, 29, 3.

16.  Fokin, A. A.; Krasutsky, P. A.; Gulevich, A.V.; Yurchenko, A. G.  Oxidation of 3,7,7-trimethyl-3,4-dihydroxybicyclo[4.1.0]heptane by molecular oxygen. Russ. J. Org. Chem. 1992, 28, 1098–1099.

15.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structures of 1R-cis-polyhalogenchrysanthemic acids. Russ. J. Org. Chem. 1992, 28, 67–75.

14.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G.  Key synthones of pyrethrinoides based on 3-carene.  Ukr. Khim. Zhurnal 1992, 58, 1130–1135.

13.  Fokin, A. A.; Fedorenko, T. V.; Yurchenko, A. G. Enantioselective synthesis of chrysanthemic acid and derivatives. Ukr. Khim. Zhurnal 1992, 58, 1120–1126.

12.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structure of the stereoisomeric monochlorochrysanthemic acids. Russ. J. Org. Chem. 1991, 27, 1279–1283.

11.  Fokin, A. A.; Krasutsky, P. A.; Baula, O. P.; Yurchenko, A. G.  Functionalization of 4,7,7-trimethyl-3-oxabicyclo[3.31]hept-4-en-2-one with dichlorocarbene. Russ. J. Org. Chem. 1991, 27, 1363.

10.  Krasutsky, P. A.; Fokin, A. A.; Rodionov, V. N.; Kulik, N. I.; Ambrosienko, N. V.; Yurchenko, A. G.  On the mechanisms of transannular acidic cyclization of 3,7-dimethylenobicyclo[3.3.1]nonane and derivatives. Russ. J. Org. Chem. 1991, 27, 992–999.

9.      Krasutsky, P. A.; Fokin, A. A.; Butova, E. D.; Yurchenko, A. G. Stereoselective synthesis of (–)-pirocine and 1R-E-chrysanthemic acid from 2-pinene. Vest. Kiev. Polytech. Inst. 1991, 28, 40–44.

8.      Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G. The structures of carbenilation products of 2-pinene and 3-carene with carboethoxycarbene. Ukr. Khim. Zhurnal 1989, 55,  842–845.

7.      Krasutsky, P. A.; Fokin, A. A.; Maleev, A. V.; Kurkutova, E. N.; Struchkov, Y. T.; Yurchenko, A. G. The structure of adducts of allenes of bicyclo[3.3.1]nonane series with dihalocarbenes. Russ. J. Org. Chem. 1990, 26, 1016–1024.

6.      Krasutsky, P. A.; Fokin, A. A.; Skoba, E. D.; Yurchenko, A. G. the synthesis and protic cyclization of 3-vinylidenobicyclo[3.3.1]nonane-7-one. Russ. J. Org. Chem. 1986, 22, 460–461.

5.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and protic cyclization of 3-vinylideno-7-propadienilidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1986, 22, 459–460.

4.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and reactivity of 3-methylene-7-vinylidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1985, 21, 2522–2626.

3.      Krasutsky, P. A.; Fokin, A. A.; Kulik, N. I.; Yurchenko, A. G. The reactivity of 3,7-divinylidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1985, 21, 2518–2522.

2.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G.; Chekmenyova, L. A. The synthesis of 3,7-divinylidenbicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1984, 20, 1807–1808.

1.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G.; Jones, M. Jr.; Antipin, M. Y.; Struchkov, Y. T. The structure of carbenylation products of 3-methylenebicyclo[3.3.1]nonane. Teoret. i Experim. Khimiya 1984, 20, 427–433.

 

 

159. Becker, J.; Zhyhadlo, Y. Y.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Ferster, M.; Holthausen, M. C.; Specht, P.; Schindler, S.  Aerobic aliphatic hydroxylation reactions by copper complexes: A simple clipandcleave concept. Chem. Eur. J.2018, 24, https://doi.org/10.1002/chem.201802607

158.Gebbie, M. A.; Ishiwata, H.;  McQuade P.J.; Petrak, V.: Taylor, A.; Freiwald, C.; Dahl, J. E.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Nesladek, M.; Melosh, N. A. Experimental measurement of the diamond nucleation landscape reveals classical and nonclassical features. PNAS, 2018, 115, 33, 8284–8289.

157. Moncea, O.; Poinsot, D.; Fokin, A. A.; Schreiner, P. R.; Hierso, J. C. Palladium-catalyzed C2-H arylation of unprotected (N-H)-indoles “On water” using primary diamantyl phosphine oxides as a class of primary phosphine oxide ligands. ChemCatChem, 2018, 10, 2915 – 2922.

155.Hoc, N. T.  Fokin, A. A; Rodionov, V. N. Towards 3-(2-adamantylidene)diamantane derivatives through the McMurry cross coupling reaction. Org. Commun. 2018, 11, 2x, 75-79.

156. Hoc, N. T.  Fokin, A. A; Rodionov, V. N. Synthesis of 10-methoxydiamantan-3-one. MOLBANK. 2018, 2, UNSP M990. DOI: 10.3390/M990

154.Yan, H.;Narasimha, K. T.; Denlinger, J.;Li, F. H.;Mo, S.-K.;Nathan Hohman, J.;  Dahl, J. E. P.; ,Carlson, R. M. K.;Tkachenko, B. A.;Fokin, A. A.; Schreiner, P. R.; Hussain, Z.; Shen, Z.-X.; ,Melosh, N. A.Monochromatic photocathodes from graphene-stabilized diamondoids. Nano Lett., 2018, 18, 1099–1103.

153.Yan, H.; Yang, F.; Pan, D.; Lin, Y.; Hohman, J. N.; Solis-Ibarra, D.; Li, F. H.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Galli, G.; Mao, W. L.; Shen Z.-X.; Melosh, N. M. Sterically controlled mechanochemistry under hydrostatic pressure. Nature 2018, 554, 505–510.

152.Gunawan, M. A.; Moncea, O.; Poinsot, D.; Keskes, M.; Domenichini, B.; Heintz, O.; Chassagnon, R.; Herbst, F.; Carlson, R. M. K.; Dahl, J. E. P.; Fokin, A. A.; Schreiner, P. R.; Hierso,  J.-C. Nanodiamond-Palladium Core–Shell Organohybrid Synthesis: A Mild Vapor-Phase Procedure Enabling Nanolayering Metal onto Functionalized sp3-Carbon. Adv. Funct. Mater. 2018, 1705786 (15 p).

151.Gunchenko, P. A.; Li,J.; Liu, B.; Chen, H.; Pashenko, A. P.;Bakhonsky, V. V.; Zhuk. T. S.; Fokin, A. A. Aerobic oxidations with N-hydroxyphthalimide in trifluoroacetic acid. Molec. Cat. 2018, 446, 72-79.

150.Zhyhadlo, Y. Y.; Gaidai, A. V.; Sharapa, D. I.; Mitlenko, A. G.; Shishkin, O. V.; Shishkina, S. V.; Levandovskiy, I. A.; Fokin, A. A. Functionalised Cookson's diketones in chlorosulfonic acid: Towards polysubstituted D3-trishomocubanes. J. Chem. Res. 2017, 41, 12, 677-733.

149.Tyborski, C.; Gillen, R.; Fokin, A. A.; Koso, T. V.; Fokina, N. A.; Hausmann, H.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. Electronic and Vibrational Properties of Diamondoid Oligomers. J. Phys. Chem. 2017, 121, 48, 27082–27088

148.     Fokin, A. A.: Zhuk, T. S.; Blomeyer, S.; Peŕez, C.;  Chernish, L.V.; Pashenko, A. E.; Antony, J.; Vishnevskiy, Y. V.;  Berger, R. J. F.; Grimme, S.; Logemann, C.; Schnell, M.; Mitzel N. W.; Schreiner P. R. Intramolecular London dispersion interaction effects on gas-phase and solid-state structures of diamondoid dimers. J. Amer. Chem. Soc. 2017, 139, 16696-16707.

147.     Tyborski, C.; Meinke, R.; Gillen, R.; Bischoff, T.; Knecht, A.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N. Schreiner, P. R.; Moller, T.; Rander, T.; Thomsen, C.; Maultzsch, J. From isolated diamondoids to a van-der-Waals crystal: A theoretical and experimental analysis of a trishomocubane and a diamantane dimer in the gas and solid phase. J. Chem. Phys. 2017, 147, 4, 044303 (6 p.)

146.     Fokin, A. A.; Pashenko, A. E.; Bakhonsky, V. V.; Zhuk. T. S.; Chernish. L. V.; Gunchenko, P. A.; Kushko, A. O.; Becker, J.; Wende, R. C.; Schreiner. P. R. Chiral building blocks based on 1,2-disubstituted diamantanes. Synthesis, 2017. 49, 20032008.

145.     Yan, H.; Hohman, J. N.; Li, F. H.; Jia, C.; Solis-Ibarra, D.; Wu, B.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Vailionis, A.; Kim, T. R.; Devereaux, T. P.; Shen, Z.-X.; Melosh. N. A. Hybrid metal–organic chalcogenide nanowires with electrically conductive inorganic core through diamondoid-directed assembly. Nat. Mater. 2017, 16, 349–355.

144.  Hoc, N. T.;Kushko, A. O.;Fokin, A. A.;Rodionov, V. N. Functional derivatives of diamantanone. Russ. J. Org. Chem. 2016, 52, 8, 1209–1211.

143.Moncea O.; Gunawan, M. A.; Poinsot,D.; Cattey. H.;Becker,J.;Yurchenko,R. I.; Butova,E. D.; Hausmann,H.; Šekutor,M.; Fokin, A. A.; Hierso,J.-C.; Schreiner, P. R. Defying stereotypes with nanodiamonds: Stable primary diamondoid phosphines,  J. Org. Chem. 2016, 81, 8759−8769.

142.     Tverdiy, D. O. Chekanov, M. O.; Savitskiy, P. V.; Syniugin, A. R.; Yarmoliuk, S. M. Fokin, A. A. Efficient preparation of imidazo[1,5-a]pyridine-1-carboxylic acids. Synthesis 2016, 48, A–I.

141.     Ponomarenko, M. V.; Grabowsky,S.; Pal,R.; Röschenthaler, G.-V., Fokin, A. A. SF5-Enolates in Ti(IV)-mediated aldol reactions. J. Org. Chem. 2016, 81, 6783−6791.

140.     Karthik, T. N.; Ge,C.; Fabbri,J. D.; Clay,W.; Tkachenko, B. A.; Fokin, A.A.; Schreiner, P. R.; Dahl, J. E.; Carlson, R. M. K.; Shen, Z. X.; Melosh, N. A. Ultra-low effective work function surfaces using diamondoid monolayers. Nature Nanotech. 2016, 11, 267–273.

139.     Zhang, J. L.; Ishiwata, H.; Babinec, T. M.; Radulaski, M.; Müller, K.; Lagoudakis, K. G.; Dory, C.; Dahl, J.; Edgington, R.; Soulière, V.; Ferro, G.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N.; Vuckovic, J. Hybrid group IV nanophotonic structures incorporating diamond silicon-vacancy color centers. Nano Lett. 2016, 16, 212−217.

138.Syniugin, A. R.; Chekanov, M. O.; Savitskiy, P. V.; Pashenko, A. E.; Zhuk, T. S.; Yarmoluk, S. M.; Fokin, A A. New method for the synthesis of pyrrolo[2,3-b]dihydroquinolines. Tetrahedron Lett.  2016, 57, 213–215.

137.Valentin, L.; Henss, A.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Becker, S.; Würtele, C.; Schindler, S. Transition metal complexes with cage-opened diamondoid tetracyclo[7.3.1.14,12.02,7]tetradeca-6.11-diene. J. Coor. Chem. 2015, 68, 3295–3301.

136.Lourie, L. F.; Serguchev, Yu. A.; Bentya, A. V.; Ponomarenko, M. V.; Rusanov, E. B.; Vovk, M. V.; Fokin, A. A.; Ignat’ev, N. V. Metal free electrophilic fluoro-cyclization of unsaturated N-hydroxy- and N-acetoxyamides with N–F reagents. J. Fluor. Chem. 2015, 179, 42–47.

135.Bremer, M.; Untenecker, H.; Gunchenko, P. A.; Fokin, A. A.; Schreiner P. R.  Inverted carbon geometries: Challenges to experiment and theory. J. Org. Chem. 2015, 80, 6520−6524.

134.     Zhuk, T. S.; Koso, T.; Pashenko, A. E.; Hoc, N. T.; Rodionov, V. N.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Toward an understanding of diamond sp2-defects with unsaturated diamondoid oligomer model. J. Am. Chem. Soc. 2015, 137, 6577−6586.

133.     Gunawan, M. A.; Poinsot, D.; Domenichini, B.; Dirand, C.; Chevalier, S.; Fokin, A. A.; Schreiner, P. R.; Hierso, J.-P. The functionalization of nanodiamonds (diamondoids) as a key parameter of their easily controlled self-assembly in micro- and nanocrystals from the vapor phase. Nanoscale, 2015, 7, 1956–1962.

132.     Barabash, A. V.; Didukh, N. A.; Kibal’nyi, N. A.; Butova, E. D.; Schreiner, P. R.;Fokin, A. A. Unusual aerobic oxidation of sterically hindered 1-diamanty methyl ketone. Russ. J. Org. Chem. 2014, 50, 1690–1691.

131.       Gunchenko, P. A.; Novikovskii, A. A.; Byk, M. V.; Fokin, A. A.  Structure and transformations of diamantane radical cation: Theory and experiment. Russ. J. Org. Chem. 2014, 50, 1749–1754.

130.Mishura, A. M.; Sklyarova, A. S.; Shamota, T. V.: Rodionov, V. N.; Fokin, A. A.  Preparative synthesis of pentacyclo[6.3.0.02,6.03,10.05,9]undecan-4-one (D3-Trishomocubanone). Russ. J. Org. Chem. 2014, 50, 1542–1544.

129.Barabash, A. V.; Butova, E. D.; Kanyuk, I. M.; Schreiner, P. R.; Fokin, A. A. Beyond the Corey reaction II: Dimethylenation of sterically congested ketones J. Org. Chem. 2014, 79, 10669−10673. ACS Editor’s Choice, 01.10.2014.

128.Randel, J. C.; Niestemski, F. C.; Botello-Mendez, A. R.; Mar, W.; Ndabashimiye, G.; Melinte, S.; Dahl, J. E. P.; Carlson R. M. K.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Charlier, J.-C.; Manoharan, H. C. Unconventional molecule-resolved current rectification in diamondoid fullerene hybrids. Nature Comm. 2014, 5, 4877 (6 p).

127.Tchernobaev, I. I.; Serguchev, Yu. A.; Fokin, A. A. Mechanism and selectivities of the chlorination of toluene in the presence of catalytical composition antimony pentachloride – benzodithio crown ether. Ukr. Krim. Zhurn. 2014, 50, 45–49.

126.Ponomarenko, M. V.; Serguchev, Yu. A.; Hirschberg, M. E.; Röschenthaler, G.-V.; Fokin, A. A. Elemental F2 with transannular dienes: Regioselectivities and mechanisms. Chem. Eur. J. 2014, 20, 10383–10391.

125.Fokin, A.A.; Yurchenko, R. I.; Tkachenko,B.A.; Fokina,N. A.; Gunawan,M. A.; Poinsot,D.; Dahl, J. E. P.; Carlson,R. M. K.; Serafin,M.; Cattey,H.; Hierso,J.-C.; Schreiner, P. R. Selective preparation of diamondoid phosphonates. J. Org. Chem. 2014, 79, 5369–5373.

124.Fokin, A. A.; Zhuk, T. S.; Pashenko, A. E.; Osipov, V. V.; Gunchenko,P. A.; Serafin, M.; Schreiner, P. R. Functionalization of homodiamantane: Oxygen insertion reactions without rearrangement with dimethyldioxirane. J. Org. Chem. 2014, 79, 1861–1866.

123.Meinke, R.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. UV resonance Raman analysis of trishomocubane and diamondoid dimers. J. Chem. Phys. 2014, 140, 034309 (5p).

122.Kahl, P.; Tkachenko, B. A.; Novikovsky, A. A.; Backer, J.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.  Efficient peparation of aically substituted damondoid drivatives, Synthesis 2014, 46, 787–798.

121.Gunawan, M. A.; Hierso, J.-C.; Poinsot, D.; Fokin, A. A.; Fokina, N. A.; Tkachenko, B. A.;Schreiner, P. R. Diamondoids: Functionalization and subsequent applications of perfectly defined molecular cage hydrocarbons. New J. Chem. 2014, 38, 28–41.

120.     Chekanov, M. O.; Ostrynska, O. V.; Tarnavskyi, S. S.; Synyugin, A. R.; Briukhovetska, N. V.; Bdzhola, V. G.; Pashenko, A. E.; Fokin A. A.; Yarmoluk, S. M. Design, synthesis and biological evaluation of 2-aminopyrimidinones and their 6-aza-analogs as a new class of СК2 inhibitors. J. Enz. Inhib. Med. Chem. 2014, 29, 5, 639­–646.

119.     Ponomarenko, M. V.; Lummer, K.; Fokin, A. A.; Serguchev, Yu. A.; Bassil,B. S.; Röschenthaler, G.-V.  Preparations of SF5- and CF3-substituted arenes utilizing the 7-oxabicyclo­[2.2.1]hept-2-ene synthones. Org. Biomol. Chem. 2013, 11, 8103­–8112.

118.     Kacharov, A. D.; Yemets, S. V.; Nemykin,V. N.; Kacharova, L. M.; Fokin,A. A.; Krasutsky, P. A. Stereoselectivity of A-ring contraction for 3-oxotriterpenoids.  RCS Advances 2013, 3, 19057–19063.

117.     Mishura,A. M.; Sklyarova,A. S.; Sharapa, D. I.; Levandovsky, I. A.; Serafin, M.; Fokin, A. A.; Rodionov, V. N. Stereoselective Preparation of mono- and bis-derivatives of pentacyclo[6.3.0.02,6.03,10.05,9]undecane (D3-trishomocubane). Open. Chem.  2013, 11, 2144–2150.

116.Li, F. H.; Fabbri, J. D.; Yurchenko, R. I.; Mileshkin, A. N.; Hohman, J. N.; Yan, H.; Yuan, H.; Tran, I. C.; Willey, T. M.; Bagge-Hansen, M.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N. A. Covalent attachment of diamondoid phosphonic acid dichlorides to tungsten oxide surfaces. Langmuir 2013, 29, 9790–9797.

115.Zimmermann, T.; Richter, R.; Knecht, A.; Fokin, A. A.; Koso, T. V.; Chernish, L. V.; Gunchenko, P. A.; Schreiner, P. R.; Moller, T.; Rander, T. Exploring covalently bound diamondoid aggregates with valence photoelectron spectroscopy. J. Chem. Phys. 2013, 139, 084310 (6 p).

114.Fokin, A. A.; Butova, E. D.; Barabash, A. V; Huu, N. N.; Tkachenko. B. A.; Fokina, N. A.; Schreiner, P. R. Preparative synthesis of vinyl diamondoids. Synth. Comm. 2013, 43, 1772–1777.

113.Sklyarova, A. S.; Rodionov, V. N.; Parsons, C. G.; Quack, G.; Schreiner, P. R.; Fokin, A. A. Preparation and testing of homocubyl amines as therapeutic NMDA receptor antagonists. Med. Chem. Res. 2013, 22, 360–366.

112.     Clay, W. A.; Maldonado, J. R.;  Pianetta, P.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Melosh, N.; Shen, Z.-X. Photocathode device using diamondoid and cesium bromide films Appl. Phys. Lett. 2012, 101, 241605 (5p).

111.Ishiwata, H.; Acremann, Y.; Scholl, A.; Rotenberg, E.; Hellwig, O.; Dobisz, E.; Doran, A.; Tkachenko, B.A.; Fokin, A.A.; Schreiner, P.R.; Dahl, J.E.P.; Carlson, R.M.K.; Melosh, N.; Shen, Z.-X.; Oldag, H. Diamondoid coating enables disruptive approach for chemical and magnetic imaging with 10 nm spatial resolution. Appl. Phys. Lett. 2012, 101, 163101 (5 p).

110.Fokin, A. A.;  Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Hausmann, H.; Serafin, M.; Dahl J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Stable alkanes containing very long carbon–carbon bonds. J. Am. Chem. Soc. 2012, 134, 1364113650.

109.     Gunchenko, P. A.; Fokin, A. A. Mechanisms of activation of C–H bonds in framework compounds: Theory and experiment. Theoret. Experim. Khim. 2012, 47, 6, 343–360.

108.     Gaidai, A. V.; Volochnyuk, D. M.; Shishkin, O. V.; Fokin, A. A.; Levandovskiy, I. A.; Shubina, T. E. D3-Trishomocubane-4-carboxylic acid as a new chiral building block: Synthesis and absolute configuration. T. E. Synthesis 2012, 44, 810–816.ю

107.Fokina, N. A.; Tkachenko, B. A.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner P. R.  Synthesis of diamondoid carboxylic acid. Synthesis 2012, 44, 259–264.1

106.Fokin, A. A.; Gerbig, D.; Schreiner, P. R. σ/σ- and π/π-Interactions are equally important: multilayered graphanes. J. Am. Chem. Soc. 2011, 133, 20036–20039.

105.Rodionov, V. N.; Sklyarova, A. S.; Shamota, T. V.; Schreiner, P. R.; Fokin, A. A. Selective reductive dimerization of homocubane series oximes. Russ. J. Org. Chem. 2011, 47, 11, 1695−1702.

104.     Schreiner, P. R.; Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Hausmann, H.; Serafin, M.; Schlecht, S.; Dahl J. E. P.; Carlson, R. M. K.; Fokin, A. A. Overcoming  lability of extremely long alkane carbon–carbon bonds through dispersion forces. Nature 2011, 477, 308–311. This paper was featured in Chemical & Engineering News, 89(38), September 19, 2011 [Science & Technology, Concentrates]

103.Novikovskii, A. A.; Gunchenko P. A.; Prikhodchenko P. G.; Serguchev, Yu. A.; Schreiner P. R.; Fokin A.A. Comparative theoretical and experimental analysis of hydrocarbon σ-radical cations. Russ. J. Org. Chem. 2011, 47, 1293–1299.

102.     Shubina, T. E.; Fokin, A. A. Hydrocarbon s-radical cations. WIREs Comput. Mol. Sci. 2011, 1 661679.

101.     Serguchev, Yu. A.; Ponomarenko, M. V.; Lourie, L. F.; Fokin, A. A. Transannular additions of selectfluor and xenon difluoride: regioselectivity and mechanism. J. Phys. Org. Chem. 2011, 24, 407–413.

100.     Butova, E. D.; Barabash, A. V.; Petrova, A. A.; Kleiner, C. M.; Schreiner, P. R.; Fokin. A. A. Stereospecific consecutive epoxide ring expansion with dimethylsulfoxonium methylide, J. Org. Chem. 2010, 75, 18, 6229–6235.

99.    Demchenko, P. Yu.; Gladyshevskii, R. E.; Volkov, S. V.; Kharkova, L. B.; Yanko, O. G.; Fokina, Z. A.; Fokin, A. A. The first nonaselenium ring. Chem. Commun. 2010, 46, 4520–4522.

98.  Lysenko, A. B.; Senchyk, G. A.; Lincke, J.; Lässig, D.; Fokin, A. A.; Butova, E. D.; Schreiner, P. R.; Krautscheid, H.; Domasevitch, K. V. Metal oxide-organic frameworks (MOOFs), a new series of coordination hybrids constructed from molybdenum(VI) oxide and bitopic 1,2,4-triazole linkers. Dalton Trans. 2010, 39, 4223–4231.

97.  Zhuk, T. S.; Bratko, E. Y.; Pashenko, A. E.; Gunchenko, P. A.; Yurchenko, A. G.; Schreiner, P. R.; Fokin, A. A. The “green” synthesis of neuroprotecting drug Memantine. J. Org. Pharm. Chem. 2010, 8, 62–66.

96.  Roth, S.; Leuenberger, D.; Osterwalder, J.; Dahl, J. E.; Carlson, R. M. K.; Tkachenko, B. A. Fokin, A. A.; Schreiner, P. R., Hengsberger, M. Negative-electron-affinity diamondoid monolayers as high-brilliance source for ultrashort electron pulses. Chem. Phys. Lett.  2010, 495, 102–108.

95.  Landt, L.; Bostedt, C.; Wolter, D.; Möller, T.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Kulesza, A.; Bonacic-Koutecky, V. Experimental and theoretical studies of the absorption properties of thiolated diamondoids. J. Chem. Phys. 2010, 132, 144305 (6p).

94.  Landt, L.; Staiger, M.; Wolter, D.; Klünder, K.; Zimmermann, P.; Willey, T. M.; van Buuren, T.; Brehmer, D.; Schreiner, P. R.; Tkachenko, B. A.; Fokin, A. A.; Möller, T.; Bostedt, C. The influence of a single thiol group on the electronic and optical properties of the smallest diamondoid adamantane. J. Chem. Phys. 2010, 132, 0247101(7p).

93.  Levandovskiy, I. A.; Shubina, T. E.; Fokin, A. A. Computational and QSAR study of the alkylnaphthyl ketones adsorption on silver-ion stationary phase.  J. Molec. Mod. 2010, 16, 513–522.

92.  Schreiner, P. R.; Fokin, A. A.; Reisenauer, H. P.;  Tkachenko, B. A.; Vass, E.; Olmstead, M. M.; Bläser, D.; Boese, R.; Dahl, J. E. P.; Carlson, R. M. K. [123]Tetramantane: Parent of a new family of σ-helicenes. J. Am. Chem. Soc. 2009, 131, 11292–11293.

91.  Fokin, A. A.; Gunchenko, P. A.; Novikovsky, A. A.; Shubina, T. E.; Chernyaev, B. V.; Dahl J. E. P.; Carlson, R. M. K.; Yurchenko, A. G.; Schreiner P. R. Photoacetylation of diamondoids: Selectivities and mechanism. Eur. J. Org. Chem. 2009, 5153–5161. This work is featured: Cover picture of the Eur. J. Org. Chem., 2009, issue 30.

90.  Fokin, A. A.; Zhuk, T. S.; Pashenko, A. E.; Dral, P. O.; Gunchenko, P. A.;Dahl, J. E. P.;Carlson, R. M. K.;Koso, T. V.;Serafin, M.; Schreiner, P. R. Oxygen-doped nanodiamonds: Synthesis and functionalizations. Org. Lett. 2009, 11, 3068–3071.

89.  Sklyarova, A. S.; Rodionov, V. N.; Fokin, A. A. A convenient preparative synthesis of pentacyclo[5.3.0.02,5.03,9.04,8]decane (C2-bishomocubane). Russ. J. Org. Chem. 2009, 45, 11, 1644−1647.

88.  Gunchenko, P. A.; Makuhina, A. M.; Novikovsky, A. A.; Yurchenko, A. G.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Structure and transformations of homoadamantane radical cation.  Theoret. and Experim. Khim. 2009, 45, 4, 246–251.

87.  Willey, T. M.; Lee, J. R. I.; Fabbri, J. D.; Wang, D.; Nielsen, M. H.; Randel, J. C.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Dahl, J. E. P.; Carlson, R. M. K.; Terminello, L. J.; Melosh, N. A.; van Buuren, T. Determining orientational structure of diamondoid thiols attached to silver using near-edge X-ray absorption fine structure spectroscopy. J. Elec. Spectr. Rel. Phen. 2009, 172, 69–77.

86.  Schwertfeger, H.; Würtele, C.; Hausmann, H.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R. Selective preparation of diamondoid fluorides. Adv. Synth. Catal. 2009, 351, 1041–1054.

85.  Fokin, A. A.; Schreiner, P. R. Band gap tuning in nanodiamonds: First principle computational studies. Molec. Phys. 2009, 107, 8–12, 823–830.

84.  Fokin, A. A.; Tkachenko, B. A.; Fokina, N.  A.; Hausmann, H.; Serafin, M.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Reactivities of the prism-shaped diamondoids [1(2)3]tetramantane and [12312]hexamantane (cyclohexamantane). Chem. Eur. J. 2009, 15, 3851–3862.

83.  Fokin, A. A.; Merz, A.; Fokina, N. A.; Schwertfeger, H.; Liu, S. L.; Dahl, J. E. P.; Carlson, R. K. M.; Schreiner, P. R.  Synthetic routes to aminotriamantanes, topological analogues of the neuroprotector memantine. Synthesis 2009, 909–912.

82.  Clay, W. A.; Liu, Z.; Yang, W.; Fabbri, J. D.; Dahl, J. E.; Carlson, R. M. K.; Sun, Y.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Pianetta, P. A.; Melosh, N.; Shen Z.-X. Origin of the monochromatic photoemission peak in diamondoid monolayers. Nano Lett. 2009, 9, 57–61.

81.  Willey, T. M.; Fabbri, J. D.; Lee, J. R. I.; Schreiner, P. R.; Fokin, A. A.; Fokina, N. A; Dahl, J. E. P.; Carlson, R. M. K.; Vance, A. L.; Yang, W.; Terminello, L. J.; van Buuren, T.; Melosh, N. A.  Near-edge X-ray absorption fine structure spectroscopy of diamondoid thiol monolayers on gold.  J. Am. Chem. Soc. 2008, 130, 10536–10544.

80.  Chernish, L. V.; Gunchenko, P. A.; Barabash, A. B.; Goreslavets, V. S.; Yurchenko, A. G.; Fokin, A. A. Selective synthesis of 1,1-diadamantane monoderivatives.  Zhurn. Org. Pharm. Khim. 2008, 6, 48–51.

79.  Zhuk, T. S.; Gunchenko, P. A.; Korovai, Ya. Yu.; Schreiner,P. R.; Fokin A. A. Mechanisms of the C–H halogenation of adamantane in the presence of N-hydroxyphthalimide.   Theoret. and Experim. Khim.  2008, 44, 1, 46–51.

78.  Schwertfeger, H; Fokin, A. A.; Schreiner, P. R. Diamonds are a chemist’s best friend: Diamondoid chemistry beyond adamantane.  Angew. Chem. Int. Ed. 2008, 47, 1022–1036.

77.  Fokin, A. A.; Yurchenko, A. G.; Rodionov, V. N.; Gunchenko, P. A.; Yurchenko, R. I.; Reichenberg, A.; Wiesner, J.; Hintz, M.; Jomaa, H.; Schreiner, P.R. Synthesis of the antimalarial drug FR900098 utilizing the nitroso-ene reaction. Org. Lett. 2007, 9, 4379–4382. G

76.  Fokina, N. A.; Tkachenko, B. A.; Merz, A.; Serafin, M.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R. Hydroxy derivatives of diamantane, triamantane, and [121]tetramantane: Selective preparation of bis-apical derivatives. Eur. J. Org. Chem. 2007, 4738–4745.

75.  Butova, E. D.; Fokin, A. A.; Schreiner, P. R. Beyond the Corey reaction: One-Step diolefination of cyclic ketones. J. Org. Chem. 2007, 72, 5689–5696.

74.  Fokin, A. A.; Butova, E. D.; Chernish, L. V.; Fokina, N. A.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Simple preparation of diamondoid 1,3-dienes via oxetane ring opening. Org. Lett. 2007, 9, 2541–2544.0

73.  Yang, W. L.; Fabbri J. D.; Willey, T. M.; Lee, J. R. I.; Dahl, J. E.; Carlson, R. M. K.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Meevasana, W.; Mannella, N.; Tanaka, K.; Zhou, X. J.; van Buuren, T.; Kelly, M. A.; Hussain, Z.; Melosh, N. A.; Shen, Z.-X. Monochromatic electronphotoemission from diamondoid monolayers. Science 2007, 316, 1460–1462.

72.       Wodrich, M. D.; Corminboeuf, C.; Schreiner, P. R.; Fokin, A. A.; Schleyer, P. v. R. How accurate are DFT treatments of organic energies? Org. Lett. 2007, 9, 1851–1854.

71.  Schreiner, P. R.; Fokin, A. A.; Pascal, R. A., Jr.; de Meijere, A. Many density functional theory approaches fail to give reliable large hydrocarbon isomer energy differences. Org. Lett. 2006, 8, 3635–3638.

70.  Fokin, A. A.; Schreiner, P. R.; Fokina, N. A.; Tkachenko, B. A.; Hausmann, H.; Serafin, M. Dahl, J. E. P.; Liu, S.; Carlson, R. M. K.  Functionalized nanodiamonds Part 4: Reactivity of [1(2,3)4]pentamantane (Td-Pentamantane): A nanoscale model of diamond J. Org. Chem. 2006, 71, 8532–8540.

69.   Ponomarenko, M. V.; Serguchev Y. A.; Ponomarenko, B. V.; Röschenthaler, G.-V.; Fokin, A. A. Experimental and theoretical studies on the transannular cyclizations of 3,7-dimethylenebicyclo[3.3.1]nonane with polyfluoroalkyl radicals.  J. Fluor. Chem, 2006, 127, 842–849.

68.  Schreiner, P. R.; Fokina, N. A.; Tkachenko, B. A.; Hausmann, H.; Serafin, M.; Dahl, J. E. P.; Liu, S.; Carlson, R. M. K.; Fokin, A. A. Functionalized Nanodiamonds Part 2: Triamantane and [121]Tetramantane. J. Org. Chem. 2006, 71, 18, 6709–6720. This work is featured: Cover picture of the J. Org. Chem., 2006, issue 18.

67.  Tkachenko, B. A.; Fokina, N. A.; Chernish, L. V.; Dahl, J. E. P.; Liu, S.; Carlson, M. K.; Fokin, A. A.; Schreiner, P. R. Functionalized Nanodiamonds Part 3: Thiolation of tertiary/bridgehead alcohols. Org. Lett. 2006, 8, 1767–1770.

66.  Fokin, A. A.; Schreiner, P. R.; Berger, R.; Robinson, G. H.; Wei, P.; Campana, C. F. Pseudotetrahedral polyhalocubanes: Synthesis, structures, and parity violating energy differences. J. Am. Chem. Soc. 2006, 128, 5332–5333. This work is featured: Nature, 2006, 44, 4, 5.

65.  Fokin, A. A.; Tkachenko, B. A.; Gunchenko, P. A. Gusev, D. V. Schreiner, P. R. Functionalized Nanodiamonds Part I. An experimental assessment of diamantane and computational predictions for higher diamondoids. Chem. Eur. J. 2005, 11, 7091–7101.

64.  de Meijere, A.; Lee, C.-H.; Kuznetsov M. A.; Gusev, D. V.; Kozhushkov, S. I.; Fokin, A. A.; Schreiner, P. R. Preparation and reactivity of [D3d]-octahedrane: The most stable (CH)12 hydrocarbon. Chem. Eur. J. 2005, 11, 6175–6184.

63.  Rodionov, V. N.; Chernyaev, B. V.; Levandovskii, I. A.; Shubina, T. E.; Fokin, A. A..  Quantum-chemical interpretation of the reorientation of dialkyl-cis-9,10-dihydroanthracene-9,10-endofumarates on a silver-containing stationary phase.  Theoret. and Experim. Khim. 2005, 41, 1, 1–6.

62.  Rodionov, V. M.; Chernyaev, B. V.; Levandovs'kii, I. A.; Shubina, T. E.; Fokin, A. A.; Yurchenko, O. G.  Experimental and quantum-chemical study of the thermodynamics of complexation of methylbenzenes with silver(I) ion.    Naukovi Visti - Natsional'nii Tekhnichnii Universitet Ukraini "Kiivs'kii Politekhnichnii Institut"  2005, 1, 107–115.

61.  Fokin, A. A.; Tkachenko, B. A.; Gunchenko, P. A.; Schreiner, P. R. The protonation of cubane revisited. Angew. Chem. Int. Ed. 2005, 44, 146–149.

60.  Schreiner, P. R.; Fokin, A. A.; Kotke, M.; Weil, T. Noncovalent organocatalysis.  Ann. Pol. Chem. Soc. 2004, 3, part 1, 21–24.

59.  Schreiner, P. R.; Fokin, A. A. Selective alkane C–H-bond functionalizations utilizing oxidative single-electron transfer and organocatalysis. Chem. Record 2004, 3, 247–257.

58.  Kiriy, N.; Jahne, E.; Adler, H.-J.; Schneider, M.; Kiriy, A.; Gorodyska, G.; Minko, S.; Jehnichen, D.; Simon,|P.; Fokin, A. A.; Stamm, M. One-dimensional aggregation of regioregular polyalkylthiophenes. Nano Letters 2003, 3, 707–712.

57.  Gunchenko, P. A.; Vigovskaya, T. S.; Fokin, A. A.; Yurchenko, A. G. A New method for building of [3.3.3]propellan skeleton.  Ukr. Khim. Zhurn. 2003, 69, 10, 113–115.

56.  Fokin, A. A.; Schreiner, P. R. Metal-free, selective alkane functionalizations.  Adv. Chem. Cat. 2003, 345, 1035–1052.

55.  de Meijere, A.; Kozhushkov, S. I.; Fokin, A. A.; Emme, I.; Redlich, S.; Schreiner, P. R. New structurally interesting cyclopropane derivatives. A world of wonders and surprises. Pure Appl. Chem. 2003, 75, 549–562.

54.  Fokin, A. A.; Schreiner, P. R.; Kozhushkov, S. I.; Sattelmeyer, K. W.; Schaefer, H. F.; de Meijere, A. Delocalizations in s-radical cations: The Intriguing structures of ionized [n]rotanes.  Org. Lett. 2003, 5, 697–700.

53.  Tkachenko, B. A.; Shubina, T. E.; Gusev, D. V.; Gunchenko, P. A.; Yurchenko, A. G.; Schreiner, P. R.; Fokin, A. A. Mechanisms of C–H Activation of Alkanes by Chromium-oxo Reagents.  Theoret. and Experim. Khim. 2003, 39, 2, 90–95.

52.   Krasutsky, P. A.; Kolomitsyn, I. V.; Botov, E. M.; Carlson, R. M.; Semenova, I. G.; Fokin, A. A. Heterolytic decarboxylation involving acyltrifluoroacetyl peroxide intermediates. Tetrahedron Lett. 2002, 43, 8687–8691.

51.  Schreiner, P. R.; Fokin, A. A.; Lauenstein, O.;  Okamoto, Y.; Wakita, T.; Rinderspacher, C; Robinson, G. H.; Vohs, J. K.; Campana.; C. F. Pseudotetrahedral polyhaloadamantanes as chirality probes: Synthesis, separation, and absolute configuration.  J. Am. Chem. Soc. 2002, 124, 13348–13349.

50.  Fokin, A. A.; Tkachenko, B. A.; Shubina, T. E.; Gunchenko, P. A.; Gusev, D. V.; Vohs, J. K.; Robinson, R. H.; Yurchenko, A. G.; Schreiner, P. R. The protoadamantane radical cation.  Eur. J. Org. Chem. 2002, 3844–3849.

49.  Shubina, T. E.; Gunchenko, P. A.; Vigovskaya, T. S.; Schreiner, P. R.; Yurchenko, A. G.; Fokin, A. A.  [3.3.2]- and [3.3.3]propellanes in reactions with oxidizing electrophiles. Teoret. i Experim. Khimiya, 2002, 38, 4, 226–231.

46.  Kiriy, A. V.; Yurchenko, A. G.; Fokin, A. A. The new [2,3]-sigmatropic rearrangement of allylsulfinyl carbanions. Russ. J. Org. Chem. 2002, 38, 3, 471–472.

48.  Fokin, A. A.; Shubina, T. E.; Gunchenko, P. A.; Isaev, S. D.; Yurchenko, A. G.; Schreiner, P. R. H-Coupled electron transfer in alkane C–H activations with halogen electrophiles. J. Am. Chem. Soc. 2002, 124, 10718–10727.

47.  Fokin, A. A.; Schreiner, P. R. Selective alkane transformations via radicals and radical cations: Insights into the activation step from experiment and theory. Chem. Rev. 2002, 102, 1551–1593.

45.  Shubina, T. E.; Gunchenko. P. A.; Yurchenko, A. G.; Schreiner, P. R.; Butova, E. D.; Fokin, A. A. Structure and transformations of 1-alkyladamantane radical cations.  Teoret. i Experim. Khimiya 2002, 38, 1, 8–13.

44.  Schreiner, P. R.; Lauenstein, O.; Butova, E. D.; Gunchenko, P. V.; Kolomitsin, I. V.; Wittkopp, A.; Feder, G.; Fokin, A. A. Selective radical reactions in multiphase systems: Phase-transfer halogenations of alkanes. Chem. Eur. J. 2001, 7, 23, 4996–5003.

43.  Fokin, A. A.; Tkachenko, B. A.; Korshunov, O. I.; Gunchenko, P. A.; Schreiner, P. R. Molecule-induced alkane homolysis with dioxiranes. J. Am. Chem. Soc. 2001, 123, 11248–11252.

42.  Prall, M.; Wittkopp, A.; Fokin, A. A.; Schreiner, P. R.  Substituent effects on the Bergman Cyclization of (Z)-1,5-hexadiyne-3-enes: A systematic computational study. J. Comp. Chem. 2001, 22, 13, 1605–1614.

41.  Fornarini, S.; Crestone, E.; Fokin, A. A. The protonation of gaseous cyclopropane. Chem. Eur. J. 2001, 7, 2916–2921.

40.  Schreiner, P. R.; Gunchenko, P. A.; Wittkopp, A.; Yaroshinsky, A. I.; Peleshanko, S. A.; Fokin, A. A.  The rearrangement of the cubane radical cation in solution. Chem. Eur. J. 2001, 7, 2739–2744.

39.  Krasutsky, P. A.; Kolomitsyn, I. V.;  Kiprof, P.;  Carlson, R. M.;  Sydorenko, N. A.; Fokin, A. A.  A Consecutive double-Criegee rearrangement using TFPAA: Stepwise conversion of homoadamantane to oxahomoadamantanes.  J. Org. Chem. 2001, 66, 1701–1707.

38.  Fokin, A. A.; Lauenstein, O.; Gunchenko, P. A.; Schreiner, P. R.  Halogenation of cubane under phase-transfer conditions: Single and double C–H-bond substitution with conservation of the cage Structure.  J. Am. Chem. Soc.  2001, 123, 1842–1847.

37.  Fokin, A. A.; Peleshanko, S. A.; Gunchenko, P. A.; Gusev, D. V.; Schreiner, P. R. Hydrocarbon activations with cerium (IV) ammonium nitrate: Free radical versus oxidative pathways. Eur. J. Org. Chem. 2000, 3357–3362.

36.  Lauenstein, O.; Fokin, A. A.; Schreiner, P. R. A combined experimental and computational study of the H/D kinetic isotope effects for bromination and iodination of aliphatic hydrocarbons under phase-transfer conditions. Org. Lett.  2000, 2201–2204.

35.  Fokin,A. A.;Schreiner,P. R.; Gunchenko, P. A.; Peleshanko, S. A.; Shubina,T. E.; Isaev, S. D.; Tarasenko, P. V.; Kulik, N. I.; Schiebel, H.-M.; YurchenkoA. G. Oxidative single electron transfer activation of s-bonds in aliphatic halogenation reactions. J. Am. Chem. Soc. 2000, 122, 7317–7326.

34.  Fokin, A. A.; Kushko, A. O.; Kirij, A. V.; Yurchenko, A. G.; Schleyer, P. v. R. Direct transformations of ketones to g-unsaturated thiols via [2,3]-sigmatropic rearrangement of allyl sulfinyl carbanions: Combined experimental and theoretical study. J. Org. Chem. 2000, 65, 2984–2995.

33.  Kolomitsin, I. V.; Krasutsky, P. A.; Sidorenko, N. V.; Yurchenko, A. G.; Fokin, A. A.  Oxidative fragmentation of tetrahydrocyclopentadiene structure. Russ. J. Org. Chem. 2000,  36, 456–457.

32.  Krasutsky, P. A.; Kolomitsin, I. V.; Kiprof, P.; Carlson, R. M.; Fokin, A. A. Observation of a stable carbocation in a consecutive Criegee rearrangement with trifluoroperacetic acid. J. Org. Chem. 2000, 65, 3926–3933.

31.  Fokin, A.A.; Kiran, B.; Bremer, M.; Yang, X.; Jiao, H.; Schleyer, P. v. R.  Which electron count rules are needed for four-centered tree-dimensional aromaticity? Chem. Eur. J.; 2000, 6, 1615–1628.

30.  Schreiner, P. R.; Lauenstein, O.; Butova, E. D.; Fokin, A. A. The first efficient iodination of unactivated, aliphatic hydrocarbons. Angew. Chem. 1999, 111 2956–2958. Angew. Chem. Int. Ed. Engl. 1999, 38, 2786–2788. This work is featured: cover picture of the Angewandte Chemie, 1999, issue 18. Chemical and Engineering News 1999 September, 20, 44. Sueddeutsche Zeitung 1999 55, October, 12, p. V2/12.

29.  Fokin, A. A.; Gunchenko, P. A.; Peleshanko, S. A.; Schleyer, P. v. R.; Schreiner, P. R. Common radical cation intermediates in cage hydrocarbon activations.  Eur. J. Org. Chem. 1999, 855–860.

28.  Kushko, A. O.; Yurchenko, A. G.; Kirij, A. V.; Likhotvorik, I. R.; Fokin, A. A.  The novel one-step method of homoallylic tiols synthesis from ketons. Russ. J. Org. Chem. 1998, 34, 776–777.

27.  Fokin, A. A.; Schreiner, P. R.; Schleyer, P. v. R.; Gunchenko, P. A. Electrophilic and oxidative activation of the central C–C Bond in [3.3.n]Propellanes: A theoretical study. J. Org. Chem. 1998,No19, 6494–6502.

26.  Fokin, A. A.; Jiao, H.; Schleyer, P. v. R. From Dodecaheptapentaene to the “[n]Trannulenes”. A new In-plane aromatic family.  J. Am. Chem. Soc. 1998, 120, 9364–9365.

25.  Schreiner, P. R.; Lauenstein, O.; Kolomitsin, I. V.; Fokin, A. A.  Selective C–H activation of aliphatic hydrocarbon under phase-transfer conditions.  Angew. Chem.; Int. Ed. 1998, 37, 1895–1897. This paper was featured in Nachr. Chem. Tech. Lab. 1998 7/8, 706. Chemical and Engineering News 1998 July, 13, 55.

24.  Fokin, A. A.; Gunchenko, P. A.; Tkachenko, B. A.; Butova, E. D.; Yurchenko, A. G.  Backside activation of s-bonds with Cr(VI)-reagents.  Tetrahedron Lett. 1997, 38, 639–642.

23.  Fokin, A. A.; Gunchenko, P. A.; Kulik, N. I.; Iksanova, S. V.; Krasutsky, P. A.; Gogoman, I. V.; Yurchenko, A. G.  NO2+-containing reagents in the electrophilic and oxidative addition to propellanic C–C bond.  Tetrahedron 1996, 52, 5857–5866.

22.  Fokin, A. A.; Gunchenko, P. A.; Krasutsky, P. A.; Yaroshinsky, A. I.; Yurchenko, A. G. Oxidation of tetracyclo[4.3.1.1.4,801,4]undecane (1,4-cyclohomoadamantane). Russ. J. Org. Chem. 1995, 31, 796–797.

21.  Fokin, A. A.; Gunchenko, P. A.; Krasutsky, P. A.; Yaroshinsky, A. I.; Yurchenko, A. G. Oxidative addition to 3,6-dehydrohomoadamantane.  Tetrahedron Lett. 1995, 36, 4479–4482.

20.  Fokin, A. A.; Gagaeva, E. A.; Krasutsky, P. A.; Yurchenko, A. G. Stereoselective epoxidation of 4,7,7-trimethyl-3-oxabicyclo[3.3.1]hept-4-en-2-one. Russ. J. Org. Chem. 1994, 30, 940–941.

19.  Fokin, A. A.; Butova, E. D.; Kolomitsin, I. V.; Gagaeva, E. A.; Kornilov, A. M.; Sorochinsky A. E. Functional derivatives of 2-carene in cyclopropane-containing pyrethroides synthesis. Russ. J. Org. Chem. 1994, 30, 669–679.

18.  Fokin, A. A.; Butova, E. D.; Gulevitch, A. V.; Yurchenko, A. G.; Krasutsky, P. A.  Novel oxidative transformations in norpinonic acid synthesis. Russ. J. Org. Chem. 1993, 29, 1075–1076.

17.  Lichotvorik, I. R.; Litvin, A. L.; Shimko, R. I.; Fokin, A. A. The insertion of dichlorocarbene into tricyclo[5.2.1.02,5]decane structure. Vest. Kiev Polytech. Inst. 1992, 29, 3.

16.  Fokin, A. A.; Krasutsky, P. A.; Gulevich, A.V.; Yurchenko, A. G.  Oxidation of 3,7,7-trimethyl-3,4-dihydroxybicyclo[4.1.0]heptane by molecular oxygen. Russ. J. Org. Chem. 1992, 28, 1098–1099.

15.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structures of 1R-cis-polyhalogenchrysanthemic acids. Russ. J. Org. Chem. 1992, 28, 67–75.

14.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G.  Key synthones of pyrethrinoides based on 3-carene.  Ukr. Khim. Zhurnal 1992, 58, 1130–1135.

13.  Fokin, A. A.; Fedorenko, T. V.; Yurchenko, A. G. Enantioselective synthesis of chrysanthemic acid and derivatives. Ukr. Khim. Zhurnal 1992, 58, 1120–1126.

12.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structure of the stereoisomeric monochlorochrysanthemic acids. Russ. J. Org. Chem. 1991, 27, 1279–1283.

11.  Fokin, A. A.; Krasutsky, P. A.; Baula, O. P.; Yurchenko, A. G.  Functionalization of 4,7,7-trimethyl-3-oxabicyclo[3.31]hept-4-en-2-one with dichlorocarbene. Russ. J. Org. Chem. 1991, 27, 1363.

10.  Krasutsky, P. A.; Fokin, A. A.; Rodionov, V. N.; Kulik, N. I.; Ambrosienko, N. V.; Yurchenko, A. G.  On the mechanisms of transannular acidic cyclization of 3,7-dimethylenobicyclo[3.3.1]nonane and derivatives. Russ. J. Org. Chem. 1991, 27, 992–999.

9.      Krasutsky, P. A.; Fokin, A. A.; Butova, E. D.; Yurchenko, A. G. Stereoselective synthesis of (–)-pirocine and 1R-E-chrysanthemic acid from 2-pinene. Vest. Kiev. Polytech. Inst. 1991, 28, 40–44.

8.      Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G. The structures of carbenilation products of 2-pinene and 3-carene with carboethoxycarbene. Ukr. Khim. Zhurnal 1989, 55,  842–845.

7.      Krasutsky, P. A.; Fokin, A. A.; Maleev, A. V.; Kurkutova, E. N.; Struchkov, Y. T.; Yurchenko, A. G. The structure of adducts of allenes of bicyclo[3.3.1]nonane series with dihalocarbenes. Russ. J. Org. Chem. 1990, 26, 1016–1024.

6.      Krasutsky, P. A.; Fokin, A. A.; Skoba, E. D.; Yurchenko, A. G. the synthesis and protic cyclization of 3-vinylidenobicyclo[3.3.1]nonane-7-one. Russ. J. Org. Chem. 1986, 22, 460–461.

5.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and protic cyclization of 3-vinylideno-7-propadienilidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1986, 22, 459–460.

4.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and reactivity of 3-methylene-7-vinylidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1985, 21, 2522–2626.

3.      Krasutsky, P. A.; Fokin, A. A.; Kulik, N. I.; Yurchenko, A. G. The reactivity of 3,7-divinylidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1985, 21, 2518–2522.

2.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G.; Chekmenyova, L. A. The synthesis of 3,7-divinylidenbicyclo[3.3.1]nonane. Russ. J. Org. Chem. 1984, 20, 1807–1808.

1.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G.; Jones, M. Jr.; Antipin, M. Y.; Struchkov, Y. T. The structure of carbenylation products of 3-methylenebicyclo[3.3.1]nonane. Teoret. i Experim. Khimiya 1984, 20, 427–433.

 

 

159. Becker, J.; Zhyhadlo, Y. Y.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Ferster, M.; Holthausen, M. C.; Specht, P.; Schindler, S.  Aerobic aliphatic hydroxylation reactions by copper complexes: A simple clip‐and‐cleave concept. Chem. Eur. J.2018, 24, https://doi.org/10.1002/chem.201802607

158.Gebbie, M. A.; Ishiwata, H.;  McQuade P.J.; Petrak, V.: Taylor, A.; Freiwald, C.; Dahl, J. E.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Nesladek, M.; Melosh, N. A. Experimental measurement of the diamond nucleation landscape reveals classical and nonclassical features. PNAS, 2018, 115, 33, 8284–8289.

157. Moncea, O.; Poinsot, D.; Fokin, A. A.; Schreiner, P. R.; Hierso, J. C. Palladium-catalyzed C2-H arylation of unprotected (N-H)-indoles “On water” using primary diamantyl phosphine oxides as a class of primary phosphine oxide ligands. ChemCatChem, 2018, 10, 2915 – 2922.

155.Hoc, N. T.  Fokin, A. A; Rodionov, V. N. Towards 3-(2-adamantylidene)diamantane derivatives through the McMurry cross coupling reaction. Org. Commun.2018, 11, 2x, 75-79.

156. Hoc, N. T.  Fokin, A. A; Rodionov, V. N. Synthesis of 10-methoxydiamantan-3-one. MOLBANK. 2018, 2, UNSP M990. DOI: 10.3390/M990

154.Yan, H.;Narasimha, K. T.; Denlinger, J.;Li, F. H.;Mo, S.-K.; Nathan Hohman, J.;  Dahl, J. E. P.; ,Carlson, R. M. K.;Tkachenko, B. A.;Fokin, A. A.; Schreiner, P. R.; Hussain, Z.; Shen, Z.-X.; ,Melosh, N. A.Monochromatic photocathodes from graphene-stabilized diamondoids. Nano Lett., 2018, 18, 1099–1103.

153.Yan, H.; Yang, F.; Pan, D.; Lin, Y.; Hohman, J. N.; Solis-Ibarra, D.; Li, F. H.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Galli, G.; Mao, W. L.; Shen Z.-X.; Melosh, N. M. Sterically controlled mechanochemistry under hydrostatic pressure. Nature2018, 554, 505–510.

152.Gunawan, M. A.; Moncea, O.; Poinsot, D.; Keskes, M.; Domenichini, B.; Heintz, O.; Chassagnon, R.; Herbst, F.; Carlson, R. M. K.; Dahl, J. E. P.; Fokin, A. A.; Schreiner, P. R.; Hierso,  J.-C. Nanodiamond-Palladium Core–Shell Organohybrid Synthesis: A Mild Vapor-Phase Procedure Enabling Nanolayering Metal onto Functionalized sp3-Carbon. Adv. Funct. Mater. 2018, 1705786 (15 p).

151.Gunchenko, P. A.; Li,J.; Liu, B.; Chen, H.; Pashenko, A. P.;Bakhonsky, V. V.; Zhuk. T. S.; Fokin, A. A. Aerobic oxidations with N-hydroxyphthalimide in trifluoroacetic acid. Molec. Cat.2018, 446, 72-79.

150.Zhyhadlo, Y. Y.; Gaidai, A. V.; Sharapa, D. I.; Mitlenko, A. G.; Shishkin, O. V.; Shishkina, S. V.; Levandovskiy, I. A.; Fokin, A. A. Functionalised Cookson's diketones in chlorosulfonic acid: Towards polysubstituted D3-trishomocubanes. J. Chem. Res.2017, 41, 12, 677-733.

149.Tyborski, C.; Gillen, R.; Fokin, A. A.; Koso, T. V.; Fokina, N. A.; Hausmann, H.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. Electronic and Vibrational Properties of Diamondoid Oligomers. J. Phys. Chem.2017, 121, 48, 27082–27088

148.Fokin, A. A.: Zhuk, T. S.; Blomeyer, S.; Peŕez, C.;  Chernish, L.V.; Pashenko, A. E.; Antony, J.; Vishnevskiy, Y. V.;  Berger, R. J. F.; Grimme, S.; Logemann, C.; Schnell, M.; Mitzel N. W.; Schreiner P. R. Intramolecular London dispersion interaction effects on gas-phase and solid-state structures of diamondoid dimers. J. Amer. Chem. Soc. 2017, 139, 16696-16707.

147.Tyborski, C.; Meinke, R.; Gillen, R.; Bischoff, T.; Knecht, A.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N. Schreiner, P. R.; Moller, T.; Rander, T.; Thomsen, C.; Maultzsch, J. From isolated diamondoids to a van-der-Waals crystal: A theoretical and experimental analysis of a trishomocubane and a diamantane dimer in the gas and solid phase. J. Chem. Phys. 2017, 147, 4, 044303 (6 p.)

146.Fokin, A. A.; Pashenko, A. E.; Bakhonsky, V. V.; Zhuk. T. S.; Chernish. L. V.; Gunchenko, P. A.; Kushko, A. O.; Becker, J.; Wende, R. C.; Schreiner. P. R. Chiral building blocks based on 1,2-disubstituted diamantanes. Synthesis, 2017. 49, 20032008.

145.     Yan, H.; Hohman, J. N.; Li, F. H.; Jia, C.; Solis-Ibarra, D.; Wu, B.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Vailionis, A.; Kim, T. R.; Devereaux, T. P.; Shen, Z.-X.; Melosh. N. A. Hybrid metal–organic chalcogenide nanowires with electrically conductive inorganic core through diamondoid-directed assembly. Nat. Mater. 2017, 16, 349–355.

144.  Hoc, N. T.;Kushko, A. O.;Fokin, A. A.;Rodionov, V. N. Functional derivatives of diamantanone. Russ. J. Org. Chem. 2016, 52, 8, 1209–1211.

143.Moncea O.; Gunawan, M. A.; Poinsot,D.; Cattey. H.;Becker,J.;Yurchenko,R. I.; Butova,E. D.; Hausmann,H.; Šekutor,M.; Fokin, A. A.; Hierso,J.-C.; Schreiner, P. R. Defying stereotypes with nanodiamonds: Stable primary diamondoid phosphines,  J. Org. Chem. 2016, 81, 8759−8769.

142.     Tverdiy, D. O. Chekanov, M. O.; Savitskiy, P. V.; Syniugin, A. R.; Yarmoliuk, S. M. Fokin, A. A. Efficient preparation of imidazo[1,5-a]pyridine-1-carboxylic acids. Synthesis 2016, 48, A–I.

141.     Ponomarenko, M. V.; Grabowsky,S.; Pal,R.; Röschenthaler, G.-V., Fokin, A. A. SF5-Enolates in Ti(IV)-mediated aldol reactions. J. Org. Chem. 2016, 81, 6783−6791.

140.Karthik, T. N.; Ge,C.; Fabbri,J. D.; Clay,W.; Tkachenko, B. A.; Fokin, A.A.; Schreiner, P. R.; Dahl, J. E.; Carlson, R. M. K.; Shen, Z. X.; Melosh, N. A. Ultra-low effective work function surfaces using diamondoid monolayers. Nature Nanotech. 2016, 11, 267–273.

139.Zhang, J. L.; Ishiwata, H.; Babinec, T. M.; Radulaski, M.; Müller, K.; Lagoudakis, K. G.; Dory, C.; Dahl, J.; Edgington, R.; Soulière, V.; Ferro, G.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N.; Vuckovic, J. Hybrid group IV nanophotonic structures incorporating diamond silicon-vacancy color centers. Nano Lett. 2016, 16, 212−217.

138.Syniugin, A. R.; Chekanov, M. O.; Savitskiy, P. V.; Pashenko, A. E.; Zhuk, T. S.; Yarmoluk, S. M.; Fokin, A A. New method for the synthesis of pyrrolo[2,3-b]dihydroquinolines. Tetrahedron Lett.  2016, 57, 213–215.

137.Valentin, L.; Henss, A.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Becker, S.; Würtele, C.; Schindler, S. Transition metal complexes with cage-opened diamondoid tetracyclo[7.3.1.14,12.02,7]tetradeca-6.11-diene. J. Coor. Chem.2015, 68, 3295–3301.

136.Lourie, L. F.; Serguchev, Yu. A.; Bentya, A. V.; Ponomarenko, M. V.; Rusanov, E. B.; Vovk, M. V.; Fokin, A. A.; Ignat’ev, N. V. Metal free electrophilic fluoro-cyclization of unsaturated N-hydroxy- and N-acetoxyamides with N–F reagents. J. Fluor. Chem.2015, 179, 42–47.

135.Bremer, M.; Untenecker, H.; Gunchenko, P. A.; Fokin, A. A.; Schreiner P. R.  Inverted carbon geometries: Challenges to experiment and theory. J. Org. Chem. 2015, 80, 6520−6524.

134.Zhuk, T. S.; Koso, T.; Pashenko, A. E.; Hoc, N. T.; Rodionov, V. N.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Toward an understanding of diamond sp2-defects with unsaturated diamondoid oligomer model. J. Am. Chem. Soc.2015, 137, 6577−6586.

133.Gunawan, M. A.; Poinsot, D.; Domenichini, B.; Dirand, C.; Chevalier, S.; Fokin, A. A.; Schreiner, P. R.; Hierso, J.-P. The functionalization of nanodiamonds (diamondoids) as a key parameter of their easily controlled self-assembly in micro- and nanocrystals from the vapor phase. Nanoscale, 2015, 7, 1956–1962.

132.Barabash, A. V.; Didukh, N. A.; Kibal’nyi, N. A.; Butova, E. D.; Schreiner, P. R.;Fokin, A. A. Unusual aerobic oxidation of sterically hindered 1-diamanty methyl ketone. Russ. J. Org. Chem. 2014, 50, 1690–1691.

131.       Gunchenko, P. A.; Novikovskii, A. A.; Byk, M. V.; Fokin, A. A.  Structure and transformations of diamantane radical cation: Theory and experiment. Russ. J. Org. Chem. 2014, 50, 1749–1754.

130.Mishura, A. M.; Sklyarova, A. S.; Shamota, T. V.: Rodionov, V. N.; Fokin, A. A.  Preparative synthesis of pentacyclo[6.3.0.02,6.03,10.05,9]undecan-4-one (D3-Trishomocubanone). Russ. J. Org. Chem. 2014, 50, 1542–1544.

129.Barabash, A. V.; Butova, E. D.; Kanyuk, I. M.; Schreiner, P. R.; Fokin, A. A. Beyond the Corey reaction II: Dimethylenation of sterically congested ketones J. Org. Chem.2014, 79, 10669−10673. ACS Editor’s Choice, 01.10.2014.

128.Randel, J. C.; Niestemski, F. C.; Botello-Mendez, A. R.; Mar, W.; Ndabashimiye, G.; Melinte, S.; Dahl, J. E. P.; Carlson R. M. K.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Charlier, J.-C.; Manoharan, H. C. Unconventional molecule-resolved current rectification in diamondoid fullerene hybrids. Nature Comm.2014, 5, 4877 (6 p).

127.Tchernobaev, I. I.; Serguchev, Yu. A.; Fokin, A. A. Mechanism and selectivities of the chlorination of toluene in the presence of catalytical composition antimony pentachloride – benzodithio crown ether. Ukr. Krim. Zhurn. 2014, 50, 45–49.

126.Ponomarenko, M. V.; Serguchev, Yu. A.; Hirschberg, M. E.; Röschenthaler, G.-V.; Fokin, A. A. Elemental F2 with transannular dienes: Regioselectivities and mechanisms. Chem. Eur. J.2014, 20, 10383–10391.

125.Fokin, A.A.; Yurchenko, R. I.; Tkachenko,B.A.; Fokina,N. A.; Gunawan,M. A.; Poinsot,D.; Dahl, J. E. P.; Carlson,R. M. K.; Serafin,M.; Cattey,H.; Hierso,J.-C.; Schreiner, P. R. Selective preparation of diamondoid phosphonates. J. Org. Chem.2014, 79, 5369–5373.

124.Fokin, A. A.; Zhuk, T. S.; Pashenko, A. E.; Osipov, V. V.; Gunchenko,P. A.; Serafin, M.; Schreiner, P. R. Functionalization of homodiamantane: Oxygen insertion reactions without rearrangement with dimethyldioxirane. J. Org. Chem. 2014, 79, 1861–1866.

123.Meinke, R.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. UV resonance Raman analysis of trishomocubane and diamondoid dimers. J. Chem. Phys. 2014, 140, 034309 (5p).

122.Kahl, P.; Tkachenko, B. A.; Novikovsky, A. A.; Backer, J.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.  Efficient peparation of aically substituted damondoid drivatives, Synthesis2014, 46, 787–798.

121.Gunawan, M. A.; Hierso, J.-C.; Poinsot, D.; Fokin, A. A.; Fokina, N. A.; Tkachenko, B. A.;Schreiner, P. R. Diamondoids: Functionalization and subsequent applications of perfectly defined molecular cage hydrocarbons. New J. Chem.2014, 38, 28–41.

120.     Chekanov, M. O.; Ostrynska, O. V.; Tarnavskyi, S. S.; Synyugin, A. R.; Briukhovetska, N. V.; Bdzhola, V. G.; Pashenko, A. E.; Fokin A. A.; Yarmoluk, S. M. Design, synthesis and biological evaluation of 2-aminopyrimidinones and their 6-aza-analogs as a new class of СК2 inhibitors. J. Enz. Inhib. Med. Chem.2014, 29, 5, 639­–646.

119.     Ponomarenko, M. V.; Lummer, K.; Fokin, A. A.; Serguchev, Yu. A.; Bassil,B. S.; Röschenthaler, G.-V.  Preparations of SF5- and CF3-substituted arenes utilizing the 7-oxabicyclo­[2.2.1]hept-2-ene synthones.Org. Biomol. Chem. 2013, 11, 8103­–8112.

118.     Kacharov, A. D.; Yemets, S. V.; Nemykin,V. N.; Kacharova, L. M.; Fokin,A. A.; Krasutsky, P. A. Stereoselectivity of A-ring contraction for 3-oxotriterpenoids.  RCS Advances2013, 3, 19057–19063.

117.     Mishura,A. M.; Sklyarova,A. S.; Sharapa, D. I.; Levandovsky, I. A.; Serafin, M.; Fokin, A. A.; Rodionov, V. N. Stereoselective Preparation of mono- and bis-derivatives of pentacyclo[6.3.0.02,6.03,10.05,9]undecane (D3-trishomocubane). Open. Chem.  2013, 11, 2144–2150.

116.Li, F. H.; Fabbri, J. D.; Yurchenko, R. I.; Mileshkin, A. N.; Hohman, J. N.; Yan, H.; Yuan, H.; Tran, I. C.; Willey, T. M.; Bagge-Hansen, M.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N. A. Covalent attachment of diamondoid phosphonic acid dichlorides to tungsten oxide surfaces. Langmuir2013, 29, 9790–9797.

115.Zimmermann, T.; Richter, R.; Knecht, A.; Fokin, A. A.; Koso, T. V.; Chernish, L. V.; Gunchenko, P. A.; Schreiner, P. R.; Moller, T.; Rander, T. Exploring covalently bound diamondoid aggregates with valence photoelectron spectroscopy. J. Chem. Phys.2013, 139, 084310 (6 p).

114.Fokin, A. A.; Butova, E. D.; Barabash, A. V; Huu, N. N.; Tkachenko. B. A.; Fokina, N. A.; Schreiner, P. R. Preparative synthesis of vinyl diamondoids. Synth. Comm. 2013, 43, 1772–1777.

113.Sklyarova, A. S.; Rodionov, V. N.; Parsons, C. G.; Quack, G.; Schreiner, P. R.; Fokin, A. A. Preparation and testing of homocubyl amines as therapeutic NMDA receptor antagonists. Med. Chem. Res. 2013, 22, 360–366.

112.     Clay, W. A.; Maldonado, J. R.;  Pianetta, P.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Melosh, N.; Shen, Z.-X. Photocathode device using diamondoid and cesium bromide films Appl. Phys. Lett. 2012, 101, 241605 (5p).

111.Ishiwata, H.; Acremann, Y.; Scholl, A.; Rotenberg, E.; Hellwig, O.; Dobisz, E.; Doran, A.; Tkachenko, B.A.; Fokin, A.A.; Schreiner, P.R.; Dahl, J.E.P.; Carlson, R.M.K.; Melosh, N.; Shen, Z.-X.; Oldag, H. Diamondoid coating enables disruptive approach for chemical and magnetic imaging with 10 nm spatial resolution. Appl. Phys. Lett. 2012, 101, 163101 (5 p).

110.Fokin, A. A.;  Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Hausmann, H.; Serafin, M.; Dahl J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Stable alkanes containing very long carbon–carbon bonds. J. Am. Chem. Soc.2012, 134, 1364113650.

109.Gunchenko, P. A.; Fokin, A. A. Mechanisms of activation of C–H bonds in framework compounds: Theory and experiment. Theoret. Experim. Khim. 2012, 47, 6, 343–360.

108.Gaidai, A. V.; Volochnyuk, D. M.; Shishkin, O. V.; Fokin, A. A.; Levandovskiy, I. A.; Shubina, T. E. D3-Trishomocubane-4-carboxylic acid as a new chiral building block: Synthesis and absolute configuration. T. E. Synthesis 2012, 44, 810–816.ю

107.Fokina, N. A.; Tkachenko, B. A.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner P. R.  Synthesis of diamondoid carboxylic acid. Synthesis2012, 44, 259–264.1

106.Fokin, A. A.; Gerbig, D.; Schreiner, P. R. σ/σ- and π/π-Interactions are equally important: multilayered graphanes. J. Am. Chem. Soc.2011, 133, 20036–20039.

105.Rodionov, V. N.; Sklyarova, A. S.; Shamota, T. V.; Schreiner, P. R.; Fokin, A. A. Selective reductive dimerization of homocubane series oximes. Russ. J. Org. Chem. 2011, 47, 11, 1695−1702.

104.     Schreiner, P. R.; Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Hausmann, H.; Serafin, M.; Schlecht, S.; Dahl J. E. P.; Carlson, R. M. K.; Fokin, A. A. Overcoming  lability of extremely long alkane carbon–carbon bonds through dispersion forces. Nature2011, 477, 308–311. This paper was featured in Chemical & Engineering News, 89(38), September 19, 2011 [Science & Technology, Concentrates]

103.Novikovskii, A. A.; Gunchenko P. A.; Prikhodchenko P. G.; Serguchev, Yu. A.; Schreiner P. R.; Fokin A.A. Comparative theoretical and experimental analysis of hydrocarbon σ-radical cations. Russ. J. Org. Chem. 2011, 47, 1293–1299.

102.     Shubina, T. E.; Fokin, A. A. Hydrocarbon s-radical cations. WIREsComput. Mol. Sci. 2011, 1 661679.

101.     Serguchev, Yu. A.; Ponomarenko, M. V.; Lourie, L. F.; Fokin, A. A. Transannular additions of selectfluor and xenon difluoride: regioselectivity and mechanism. J. Phys. Org. Chem.2011, 24, 407–413.

100.     Butova, E. D.; Barabash, A. V.; Petrova, A. A.; Kleiner, C. M.; Schreiner, P. R.; Fokin. A. A. Stereospecific consecutive epoxide ring expansion with dimethylsulfoxonium methylide, J. Org. Chem.2010, 75, 18, 6229–6235.

99.    Demchenko, P. Yu.; Gladyshevskii, R. E.; Volkov, S. V.; Kharkova, L. B.; Yanko, O. G.; Fokina, Z. A.; Fokin, A. A. The first nonaselenium ring. Chem. Commun.2010, 46, 4520–4522.

98.  Lysenko, A. B.; Senchyk, G. A.; Lincke, J.; Lässig, D.; Fokin, A. A.; Butova, E. D.; Schreiner, P. R.; Krautscheid, H.; Domasevitch, K. V. Metal oxide-organic frameworks (MOOFs), a new series of coordination hybrids constructed from molybdenum(VI) oxide and bitopic 1,2,4-triazole linkers. Dalton Trans.2010, 39, 4223–4231.

97.  Zhuk, T. S.; Bratko, E. Y.; Pashenko, A. E.; Gunchenko, P. A.; Yurchenko, A. G.; Schreiner, P. R.; Fokin, A. A. The “green” synthesis of neuroprotecting drug Memantine. J. Org. Pharm. Chem. 2010, 8, 62–66.

96.  Roth, S.; Leuenberger, D.; Osterwalder, J.; Dahl, J. E.; Carlson, R. M. K.; Tkachenko, B. A. Fokin, A. A.; Schreiner, P. R., Hengsberger, M. Negative-electron-affinity diamondoid monolayers as high-brilliance source for ultrashort electron pulses. Chem. Phys. Lett.  2010, 495, 102–108.

95.  Landt, L.; Bostedt, C.; Wolter, D.; Möller, T.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Kulesza, A.; Bonacic-Koutecky, V. Experimental and theoretical studies of the absorption properties of thiolated diamondoids. J. Chem. Phys. 2010, 132, 144305 (6p).

94.  Landt, L.; Staiger, M.; Wolter, D.; Klünder, K.; Zimmermann, P.; Willey, T. M.; van Buuren, T.; Brehmer, D.; Schreiner, P. R.; Tkachenko, B. A.; Fokin, A. A.; Möller, T.; Bostedt, C. The influence of a single thiol group on the electronic and optical properties of the smallest diamondoid adamantane. J. Chem. Phys. 2010, 132, 0247101(7p).

93.  Levandovskiy, I. A.; Shubina, T. E.; Fokin, A. A. Computational and QSAR study of the alkylnaphthyl ketones adsorption on silver-ion stationary phase.  J. Molec. Mod.2010, 16, 513–522.

92.  Schreiner, P. R.; Fokin, A. A.; Reisenauer, H. P.;  Tkachenko, B. A.; Vass, E.; Olmstead, M. M.; Bläser, D.; Boese, R.; Dahl, J. E. P.; Carlson, R. M. K. [123]Tetramantane: Parent of a new family of σ-helicenes. J. Am. Chem. Soc.2009, 131, 11292–11293.

91.  Fokin, A. A.; Gunchenko, P. A.; Novikovsky, A. A.; Shubina, T. E.; Chernyaev, B. V.; Dahl J. E. P.; Carlson, R. M. K.; Yurchenko, A. G.; Schreiner P. R. Photoacetylation of diamondoids: Selectivities and mechanism. Eur. J. Org. Chem. 2009, 5153–5161. This work is featured: Cover picture of the Eur.J. Org. Chem., 2009, issue 30.

90.  Fokin, A. A.; Zhuk, T. S.; Pashenko, A. E.; Dral, P. O.; Gunchenko, P. A.;Dahl, J. E. P.;Carlson, R. M. K.;Koso, T. V.;Serafin, M.; Schreiner, P. R. Oxygen-doped nanodiamonds: Synthesis and functionalizations.Org. Lett.2009, 11, 3068–3071.

89.  Sklyarova, A. S.; Rodionov, V. N.; Fokin, A. A. A convenient preparative synthesis of pentacyclo[5.3.0.02,5.03,9.04,8]decane (C2-bishomocubane). Russ. J. Org. Chem.2009, 45, 11, 1644−1647.

88.  Gunchenko, P. A.; Makuhina, A. M.; Novikovsky, A. A.; Yurchenko, A. G.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Structure and transformations of homoadamantane radical cation.  Theoret. and Experim. Khim. 2009, 45, 4, 246–251.

87.  Willey, T. M.; Lee, J. R. I.; Fabbri, J. D.; Wang, D.; Nielsen, M. H.; Randel, J. C.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Dahl, J. E. P.; Carlson, R. M. K.; Terminello, L. J.; Melosh, N. A.; van Buuren, T. Determining orientational structure of diamondoid thiols attached to silver using near-edge X-ray absorption fine structure spectroscopy. J. Elec. Spectr. Rel. Phen.2009, 172, 69–77.

86.  Schwertfeger, H.; Würtele, C.; Hausmann, H.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R. Selective preparation of diamondoid fluorides. Adv. Synth. Catal.2009, 351, 1041–1054.

85.  Fokin, A. A.; Schreiner, P. R. Band gap tuning in nanodiamonds: First principle computational studies. Molec. Phys.2009, 107, 8–12, 823–830.

84.  Fokin, A. A.; Tkachenko, B. A.; Fokina, N.  A.; Hausmann, H.; Serafin, M.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Reactivities of the prism-shaped diamondoids [1(2)3]tetramantane and [12312]hexamantane (cyclohexamantane). Chem. Eur. J.2009, 15, 3851–3862.

83.  Fokin, A. A.; Merz, A.; Fokina, N. A.; Schwertfeger, H.; Liu, S. L.; Dahl, J. E. P.; Carlson, R. K. M.; Schreiner, P. R.  Synthetic routes to aminotriamantanes, topological analogues of the neuroprotector memantine. Synthesis 2009, 909–912.

82.  Clay, W. A.; Liu, Z.; Yang, W.; Fabbri, J. D.; Dahl, J. E.; Carlson, R. M. K.; Sun, Y.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Pianetta, P. A.; Melosh, N.; Shen Z.-X. Origin of the monochromatic photoemission peak in diamondoid monolayers. Nano Lett.2009, 9, 57–61.

81.  Willey, T. M.; Fabbri, J. D.; Lee, J. R. I.; Schreiner, P. R.; Fokin, A. A.; Fokina, N. A; Dahl, J. E. P.; Carlson, R. M. K.; Vance, A. L.; Yang, W.; Terminello, L. J.; van Buuren, T.; Melosh, N. A.  Near-edge X-ray absorption fine structure spectroscopy of diamondoid thiol monolayers on gold.  J. Am. Chem. Soc. 2008, 130, 10536–10544.

80.  Chernish, L. V.; Gunchenko, P. A.; Barabash, A. B.; Goreslavets, V. S.; Yurchenko, A. G.; Fokin, A. A. Selective synthesis of 1,1-diadamantane monoderivatives.  Zhurn. Org. Pharm. Khim.2008, 6, 48–51.

79.  Zhuk, T. S.; Gunchenko, P. A.; Korovai, Ya. Yu.; Schreiner,P. R.; Fokin A. A. Mechanisms of the C–H halogenation of adamantane in the presence of N-hydroxyphthalimide.   Theoret. and Experim. Khim.  2008, 44, 1, 46–51.

78.  Schwertfeger, H; Fokin, A. A.; Schreiner, P. R. Diamonds are a chemist’s best friend: Diamondoid chemistry beyond adamantane.  Angew. Chem. Int. Ed.2008, 47, 1022–1036.

77.  Fokin, A. A.; Yurchenko, A. G.; Rodionov, V. N.; Gunchenko, P. A.; Yurchenko, R. I.; Reichenberg, A.; Wiesner, J.; Hintz, M.; Jomaa, H.; Schreiner, P.R. Synthesis of the antimalarial drug FR900098 utilizing the nitroso-ene reaction. Org. Lett. 2007, 9, 4379–4382. G

76.  Fokina, N. A.; Tkachenko, B. A.; Merz, A.; Serafin, M.; Dahl, J. E. P.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R. Hydroxy derivatives of diamantane, triamantane, and [121]tetramantane: Selective preparation of bis-apical derivatives. Eur. J. Org. Chem. 2007, 4738–4745.

75.  Butova, E. D.; Fokin, A. A.; Schreiner, P. R. Beyond the Corey reaction: One-Step diolefination of cyclic ketones. J. Org. Chem.2007, 72, 5689–5696.

74.  Fokin, A. A.; Butova, E. D.; Chernish, L. V.; Fokina, N. A.; Dahl, J. E. P.; Carlson, R. M. K.; Schreiner, P. R. Simple preparation of diamondoid 1,3-dienes via oxetane ring opening. Org. Lett.2007, 9, 2541–2544.0

73.  Yang, W. L.; Fabbri J. D.; Willey, T. M.; Lee, J. R. I.; Dahl, J. E.; Carlson, R. M. K.; Schreiner, P. R.; Fokin, A. A.; Tkachenko, B. A.; Fokina, N. A.; Meevasana, W.; Mannella, N.; Tanaka, K.; Zhou, X. J.; van Buuren, T.; Kelly, M. A.; Hussain, Z.; Melosh, N. A.; Shen, Z.-X. Monochromatic electronphotoemission from diamondoid monolayers. Science2007, 316, 1460–1462.

72.       Wodrich, M. D.; Corminboeuf, C.; Schreiner, P. R.; Fokin, A. A.; Schleyer, P. v. R. How accurate are DFT treatments of organic energies? Org. Lett.2007, 9, 1851–1854.

71.  Schreiner, P. R.; Fokin, A. A.; Pascal, R. A., Jr.; de Meijere, A. Many density functional theory approaches fail to give reliable large hydrocarbon isomer energy differences. Org. Lett. 2006, 8, 3635–3638.

70.  Fokin, A. A.; Schreiner, P. R.; Fokina, N. A.; Tkachenko, B. A.; Hausmann, H.; Serafin, M. Dahl, J. E. P.; Liu, S.; Carlson, R. M. K.  Functionalized nanodiamonds Part 4: Reactivity of [1(2,3)4]pentamantane (Td-Pentamantane): A nanoscale model of diamond J. Org. Chem. 2006, 71, 8532–8540.

69.   Ponomarenko, M. V.; Serguchev Y. A.; Ponomarenko, B. V.; Röschenthaler, G.-V.; Fokin, A. A. Experimental and theoretical studies on the transannular cyclizations of 3,7-dimethylenebicyclo[3.3.1]nonane with polyfluoroalkyl radicals.  J. Fluor. Chem,2006, 127, 842–849.

68.  Schreiner, P. R.; Fokina, N. A.; Tkachenko, B. A.; Hausmann, H.; Serafin, M.; Dahl, J. E. P.; Liu, S.; Carlson, R. M. K.; Fokin, A. A. Functionalized Nanodiamonds Part 2: Triamantane and [121]Tetramantane. J. Org. Chem.2006, 71, 18, 6709–6720. This work is featured: Cover picture of the J. Org. Chem., 2006, issue 18.

67.  Tkachenko, B. A.; Fokina, N. A.; Chernish, L. V.; Dahl, J. E. P.; Liu, S.; Carlson, M. K.; Fokin, A. A.; Schreiner, P. R. Functionalized Nanodiamonds Part 3: Thiolation of tertiary/bridgehead alcohols. Org. Lett. 2006, 8, 1767–1770.

66.  Fokin, A. A.; Schreiner, P. R.; Berger, R.; Robinson, G. H.; Wei, P.; Campana, C. F. Pseudotetrahedral polyhalocubanes: Synthesis, structures, and parity violating energy differences. J. Am. Chem. Soc.2006, 128, 5332–5333. This work is featured:Nature, 2006, 44, 4, 5.

65.  Fokin, A. A.; Tkachenko, B. A.; Gunchenko, P. A. Gusev, D. V. Schreiner, P. R. Functionalized Nanodiamonds Part I. An experimental assessment of diamantane and computational predictions for higher diamondoids. Chem. Eur. J.2005, 11, 7091–7101.

64.  de Meijere, A.; Lee, C.-H.; Kuznetsov M. A.; Gusev, D. V.; Kozhushkov, S. I.; Fokin, A. A.; Schreiner, P. R. Preparation and reactivity of [D3d]-octahedrane: The most stable (CH)12 hydrocarbon. Chem. Eur. J. 2005, 11, 6175–6184.

63.  Rodionov, V. N.; Chernyaev, B. V.; Levandovskii, I. A.; Shubina, T. E.; Fokin, A. A..  Quantum-chemical interpretation of the reorientation of dialkyl-cis-9,10-dihydroanthracene-9,10-endofumarates on a silver-containing stationary phase.  Theoret. and Experim. Khim. 2005, 41, 1, 1–6.

62.  Rodionov, V. M.; Chernyaev, B. V.; Levandovs'kii, I. A.; Shubina, T. E.; Fokin, A. A.; Yurchenko, O. G.  Experimental and quantum-chemical study of the thermodynamics of complexation of methylbenzenes with silver(I) ion.Naukovi Visti - Natsional'nii Tekhnichnii Universitet Ukraini "Kiivs'kii Politekhnichnii Institut"  2005, 1, 107–115.

61.  Fokin, A. A.; Tkachenko, B. A.; Gunchenko, P. A.; Schreiner, P. R. The protonation of cubane revisited. Angew. Chem. Int. Ed. 2005, 44, 146–149.

60.  Schreiner, P. R.; Fokin, A. A.; Kotke, M.; Weil, T. Noncovalent organocatalysis.  Ann. Pol. Chem. Soc. 2004, 3, part 1, 21–24.

59.  Schreiner, P. R.; Fokin, A. A. Selective alkane C–H-bond functionalizations utilizing oxidative single-electron transfer and organocatalysis. Chem. Record2004, 3, 247–257.

58.  Kiriy, N.; Jahne, E.; Adler, H.-J.; Schneider, M.; Kiriy, A.; Gorodyska, G.; Minko, S.; Jehnichen, D.; Simon,|P.; Fokin, A. A.; Stamm, M. One-dimensional aggregation of regioregular polyalkylthiophenes. Nano Letters 2003, 3, 707–712.

57.  Gunchenko, P. A.; Vigovskaya, T. S.; Fokin, A. A.; Yurchenko, A. G. A New method for building of [3.3.3]propellan skeleton.  Ukr. Khim. Zhurn. 2003, 69, 10, 113–115.

56.  Fokin, A. A.; Schreiner, P. R. Metal-free, selective alkane functionalizations.  Adv. Chem. Cat. 2003, 345, 1035–1052.

55.  de Meijere, A.; Kozhushkov, S. I.; Fokin, A. A.; Emme, I.; Redlich, S.; Schreiner, P. R. New structurally interesting cyclopropane derivatives. A world of wonders and surprises. Pure Appl. Chem. 2003, 75, 549–562.

54.  Fokin, A. A.; Schreiner, P. R.; Kozhushkov, S. I.; Sattelmeyer, K. W.; Schaefer, H. F.; de Meijere, A. Delocalizations in s-radical cations: The Intriguing structures of ionized [n]rotanes.  Org. Lett. 2003, 5, 697–700.

53.  Tkachenko, B. A.; Shubina, T. E.; Gusev, D. V.; Gunchenko, P. A.; Yurchenko, A. G.; Schreiner, P. R.; Fokin, A. A. Mechanisms of C–H Activation of Alkanes by Chromium-oxo Reagents.  Theoret. and Experim. Khim.2003, 39, 2, 90–95.

52.   Krasutsky, P. A.; Kolomitsyn, I. V.; Botov, E. M.; Carlson, R. M.; Semenova, I. G.; Fokin, A. A. Heterolytic decarboxylation involving acyltrifluoroacetyl peroxide intermediates. Tetrahedron Lett. 2002, 43, 8687–8691.

51.  Schreiner, P. R.; Fokin, A. A.; Lauenstein, O.;  Okamoto, Y.; Wakita, T.; Rinderspacher, C; Robinson, G. H.; Vohs, J. K.; Campana.; C. F. Pseudotetrahedral polyhaloadamantanes as chirality probes: Synthesis, separation, and absolute configuration.  J. Am. Chem. Soc.2002, 124, 13348–13349.

50.  Fokin, A. A.; Tkachenko, B. A.; Shubina, T. E.; Gunchenko, P. A.; Gusev, D. V.; Vohs, J. K.; Robinson, R. H.; Yurchenko, A. G.; Schreiner, P. R. The protoadamantane radical cation.  Eur. J. Org. Chem. 2002, 3844–3849.

49.  Shubina, T. E.; Gunchenko, P. A.; Vigovskaya, T. S.; Schreiner, P. R.; Yurchenko, A. G.; Fokin, A. A.  [3.3.2]- and [3.3.3]propellanes in reactions with oxidizing electrophiles. Teoret. i Experim. Khimiya, 2002, 38, 4, 226–231.

46.  Kiriy, A. V.; Yurchenko, A. G.; Fokin, A. A. The new [2,3]-sigmatropic rearrangement of allylsulfinyl carbanions. Russ. J. Org. Chem. 2002, 38, 3, 471–472.

48.  Fokin, A. A.; Shubina, T. E.; Gunchenko, P. A.; Isaev, S. D.; Yurchenko, A. G.; Schreiner, P. R. H-Coupled electron transfer in alkane C–H activations with halogen electrophiles. J. Am. Chem. Soc.2002, 124, 10718–10727.

47.  Fokin, A. A.; Schreiner, P. R. Selective alkane transformations via radicals and radical cations: Insights into the activation step from experiment and theory. Chem. Rev. 2002, 102, 1551–1593.

45.  Shubina, T. E.; Gunchenko. P. A.; Yurchenko, A. G.; Schreiner, P. R.; Butova, E. D.; Fokin, A. A. Structure and transformations of 1-alkyladamantane radical cations.  Teoret. i Experim. Khimiya2002, 38, 1, 8–13.

44.  Schreiner, P. R.; Lauenstein, O.; Butova, E. D.; Gunchenko, P. V.; Kolomitsin, I. V.; Wittkopp, A.; Feder, G.; Fokin, A. A. Selective radical reactions in multiphase systems: Phase-transfer halogenations of alkanes. Chem. Eur. J.2001, 7, 23, 4996–5003.

43.  Fokin, A. A.; Tkachenko, B. A.; Korshunov, O. I.; Gunchenko, P. A.; Schreiner, P. R. Molecule-induced alkane homolysis with dioxiranes. J. Am. Chem. Soc.2001, 123, 11248–11252.

42.  Prall, M.; Wittkopp, A.; Fokin, A. A.; Schreiner, P. R.  Substituent effects on the Bergman Cyclization of (Z)-1,5-hexadiyne-3-enes: A systematic computational study. J. Comp. Chem.2001, 22, 13, 1605–1614.

41.  Fornarini, S.; Crestone, E.; Fokin, A. A. The protonation of gaseous cyclopropane. Chem. Eur. J.2001,7, 2916–2921.

40.  Schreiner, P. R.; Gunchenko, P. A.; Wittkopp, A.; Yaroshinsky, A. I.; Peleshanko, S. A.; Fokin, A. A.  The rearrangement of the cubane radical cation in solution. Chem. Eur. J. 2001, 7, 2739–2744.

39.  Krasutsky, P. A.; Kolomitsyn, I. V.;  Kiprof, P.; Carlson, R. M.; Sydorenko, N. A.; Fokin, A. A.  A Consecutive double-Criegee rearrangement using TFPAA: Stepwise conversion of homoadamantane to oxahomoadamantanes.  J. Org. Chem.2001, 66, 1701–1707.

38.  Fokin, A. A.; Lauenstein, O.; Gunchenko, P. A.; Schreiner, P. R.  Halogenation of cubane under phase-transfer conditions: Single and double C–H-bond substitution with conservation of the cage Structure.  J. Am. Chem. Soc.  2001, 123, 1842–1847.

37.  Fokin, A. A.; Peleshanko, S. A.; Gunchenko, P. A.; Gusev, D. V.; Schreiner, P. R. Hydrocarbon activations with cerium (IV) ammonium nitrate: Free radical versus oxidative pathways. Eur. J. Org. Chem.2000, 3357–3362.

36.  Lauenstein, O.; Fokin, A. A.; Schreiner, P. R. A combined experimental and computational study of the H/D kinetic isotope effects for bromination and iodination of aliphatic hydrocarbons under phase-transfer conditions. Org. Lett.  2000, 2201–2204.

35.  Fokin,A. A.;Schreiner,P. R.; Gunchenko, P. A.; Peleshanko, S. A.; Shubina,T. E.; Isaev, S. D.; Tarasenko, P. V.; Kulik, N. I.; Schiebel, H.-M.; YurchenkoA. G. Oxidative single electron transfer activation of s-bonds in aliphatic halogenation reactions. J. Am. Chem. Soc. 2000, 122, 7317–7326.

34.  Fokin, A. A.; Kushko, A. O.; Kirij, A. V.; Yurchenko, A. G.; Schleyer, P. v. R. Direct transformations of ketones to g-unsaturated thiols via [2,3]-sigmatropic rearrangement of allyl sulfinyl carbanions: Combined experimental and theoretical study. J. Org. Chem. 2000, 65, 2984–2995.

33.  Kolomitsin, I. V.; Krasutsky, P. A.; Sidorenko, N. V.; Yurchenko, A. G.; Fokin, A. A.  Oxidative fragmentation of tetrahydrocyclopentadiene structure. Russ. J. Org. Chem.2000,  36, 456–457.

32.  Krasutsky, P. A.; Kolomitsin, I. V.; Kiprof, P.; Carlson, R. M.; Fokin, A. A. Observation of a stable carbocation in a consecutive Criegee rearrangement with trifluoroperacetic acid. J. Org. Chem.2000, 65, 3926–3933.

31.  Fokin, A.A.; Kiran, B.; Bremer, M.; Yang, X.; Jiao, H.; Schleyer, P. v. R.  Which electron count rules are needed for four-centered tree-dimensional aromaticity? Chem. Eur. J.;2000, 6, 1615–1628.

30.  Schreiner, P. R.; Lauenstein, O.; Butova, E. D.; Fokin, A. A. The first efficient iodination of unactivated, aliphatic hydrocarbons. Angew. Chem.1999, 111 2956–2958. Angew. Chem. Int. Ed. Engl. 1999, 38, 2786–2788. This work is featured: cover picture of the Angewandte Chemie, 1999, issue 18. Chemical and Engineering News 1999 September, 20, 44. Sueddeutsche Zeitung 1999 55, October, 12, p. V2/12.

29.  Fokin, A. A.; Gunchenko, P. A.; Peleshanko, S. A.; Schleyer, P. v. R.; Schreiner, P. R. Common radical cation intermediates in cage hydrocarbon activations.  Eur. J. Org. Chem.1999, 855–860.

28.  Kushko, A. O.; Yurchenko, A. G.; Kirij, A. V.; Likhotvorik, I. R.; Fokin, A. A.  The novel one-step method of homoallylic tiols synthesis from ketons. Russ. J. Org. Chem.1998, 34, 776–777.

27.  Fokin, A. A.; Schreiner, P. R.; Schleyer, P. v. R.; Gunchenko, P. A. Electrophilic and oxidative activation of the central C–C Bond in [3.3.n]Propellanes: A theoretical study. J. Org. Chem.1998,No19, 6494–6502.

26.  Fokin, A. A.; Jiao, H.; Schleyer, P. v. R. From Dodecaheptapentaene to the “[n]Trannulenes”. A new In-plane aromatic family.  J. Am. Chem. Soc.1998, 120, 9364–9365.

25.  Schreiner, P. R.; Lauenstein, O.; Kolomitsin, I. V.; Fokin, A. A.  Selective C–H activation of aliphatic hydrocarbon under phase-transfer conditions.  Angew. Chem.; Int. Ed. 1998, 37, 1895–1897. This paper was featured in Nachr. Chem. Tech. Lab. 1998 7/8, 706. Chemical and Engineering News 1998 July, 13, 55.

24.  Fokin, A. A.; Gunchenko, P. A.; Tkachenko, B. A.; Butova, E. D.; Yurchenko, A. G.  Backside activation of s-bonds with Cr(VI)-reagents. Tetrahedron Lett. 1997, 38, 639–642.

23.  Fokin, A. A.; Gunchenko, P. A.; Kulik, N. I.; Iksanova, S. V.; Krasutsky, P. A.; Gogoman, I. V.; Yurchenko, A. G.  NO2+-containing reagents in the electrophilic and oxidative addition to propellanic C–C bond.  Tetrahedron1996, 52, 5857–5866.

22.  Fokin, A. A.; Gunchenko, P. A.; Krasutsky, P. A.; Yaroshinsky, A. I.; Yurchenko, A. G. Oxidation of tetracyclo[4.3.1.1.4,801,4]undecane (1,4-cyclohomoadamantane). Russ. J. Org. Chem.1995, 31, 796–797.

21.  Fokin, A. A.; Gunchenko, P. A.; Krasutsky, P. A.; Yaroshinsky, A. I.; Yurchenko, A. G. Oxidative addition to 3,6-dehydrohomoadamantane.  TetrahedronLett. 1995, 36, 4479–4482.

20.  Fokin, A. A.; Gagaeva, E. A.; Krasutsky, P. A.; Yurchenko, A. G. Stereoselective epoxidation of 4,7,7-trimethyl-3-oxabicyclo[3.3.1]hept-4-en-2-one. Russ. J. Org. Chem.1994, 30, 940–941.

19.  Fokin, A. A.; Butova, E. D.; Kolomitsin, I. V.; Gagaeva, E. A.; Kornilov, A. M.; Sorochinsky A. E. Functional derivatives of 2-carene in cyclopropane-containing pyrethroides synthesis. Russ. J. Org. Chem. 1994, 30, 669–679.

18.  Fokin, A. A.; Butova, E. D.; Gulevitch, A. V.; Yurchenko, A. G.; Krasutsky, P. A.  Novel oxidative transformations in norpinonic acid synthesis. Russ. J. Org. Chem.1993, 29, 1075–1076.

17.  Lichotvorik, I. R.; Litvin, A. L.; Shimko, R. I.; Fokin, A. A. The insertion of dichlorocarbene into tricyclo[5.2.1.02,5]decane structure. Vest. Kiev Polytech. Inst. 1992, 29, 3.

16.  Fokin, A. A.; Krasutsky, P. A.; Gulevich, A.V.; Yurchenko, A. G.  Oxidation of 3,7,7-trimethyl-3,4-dihydroxybicyclo[4.1.0]heptane by molecular oxygen. Russ. J. Org. Chem.1992, 28, 1098–1099.

15.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structures of 1R-cis-polyhalogenchrysanthemic acids. Russ. J. Org. Chem.1992, 28, 67–75.

14.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G.  Key synthones of pyrethrinoides based on 3-carene. Ukr. Khim. Zhurnal 1992, 58, 1130–1135.

13.  Fokin, A. A.; Fedorenko, T. V.; Yurchenko, A. G. Enantioselective synthesis of chrysanthemic acid and derivatives. Ukr. Khim. Zhurnal 1992, 58, 1120–1126.

12.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structure of the stereoisomeric monochlorochrysanthemic acids. Russ. J. Org. Chem.1991, 27, 1279–1283.

11.  Fokin, A. A.; Krasutsky, P. A.; Baula, O. P.; Yurchenko, A. G.  Functionalization of 4,7,7-trimethyl-3-oxabicyclo[3.31]hept-4-en-2-one with dichlorocarbene. Russ. J. Org. Chem.1991, 27, 1363.

10.  Krasutsky, P. A.; Fokin, A. A.; Rodionov, V. N.; Kulik, N. I.; Ambrosienko, N. V.; Yurchenko, A. G.  On the mechanisms of transannular acidic cyclization of 3,7-dimethylenobicyclo[3.3.1]nonane and derivatives. Russ. J. Org. Chem.1991, 27, 992–999.

9.      Krasutsky, P. A.; Fokin, A. A.; Butova, E. D.; Yurchenko, A. G. Stereoselective synthesis of (–)-pirocine and 1R-E-chrysanthemic acid from 2-pinene. Vest. Kiev. Polytech. Inst. 1991, 28, 40–44.

8.      Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Yurchenko, A. G. The structures of carbenilation products of 2-pinene and 3-carene with carboethoxycarbene. Ukr. Khim. Zhurnal1989, 55,  842–845.

7.      Krasutsky, P. A.; Fokin, A. A.; Maleev, A. V.; Kurkutova, E. N.; Struchkov, Y. T.; Yurchenko, A. G. The structure of adducts of allenes of bicyclo[3.3.1]nonane series with dihalocarbenes. Russ. J. Org. Chem.1990, 26, 1016–1024.

6.      Krasutsky, P. A.; Fokin, A. A.; Skoba, E. D.; Yurchenko, A. G. the synthesis and protic cyclization of 3-vinylidenobicyclo[3.3.1]nonane-7-one. Russ. J. Org. Chem.1986, 22, 460–461.

5.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and protic cyclization of 3-vinylideno-7-propadienilidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem.1986, 22, 459–460.

4.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and reactivity of 3-methylene-7-vinylidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem.1985, 21, 2522–2626.

3.      Krasutsky, P. A.; Fokin, A. A.; Kulik, N. I.; Yurchenko, A. G. The reactivity of 3,7-divinylidenobicyclo[3.3.1]nonane. Russ. J. Org. Chem.1985, 21, 2518–2522.

2.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G.; Chekmenyova, L. A. The synthesis of 3,7-divinylidenbicyclo[3.3.1]nonane. Russ. J. Org. Chem.1984, 20, 1807–1808.

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159. Becker, J.; Zhyhadlo, Y. Y.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Ferster, M.; Holthausen, M. C.; Specht, P.; Schindler, S.  Aerobic aliphatic hydroxylation reactions by copper complexes: A simple clipandcleave concept. Chem. Eur. J. 2018, 24, https://doi.org/10.1002/chem.201802607

158.Gebbie, M. A.; Ishiwata, H.;  McQuade P.J.; Petrak, V.: Taylor, A.; Freiwald, C.; Dahl, J. E.; Carlson, R. M. K.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Nesladek, M.; Melosh, N. A. Experimental measurement of the diamond nucleation landscape reveals classical and nonclassical features. PNAS, 2018, 115, 33, 8284–8289.

157. Moncea, O.; Poinsot, D.; Fokin, A. A.; Schreiner, P. R.; Hierso, J. C. Palladium-catalyzed C2-H arylation of unprotected (N-H)-indoles “On water” using primary diamantyl phosphine oxides as a class of primary phosphine oxide ligands. ChemCatChem, 2018, 10, 2915 – 2922.

155.Hoc, N. T.  Fokin, A. A; Rodionov, V. N. Towards 3-(2-adamantylidene)diamantane derivatives through the McMurry cross coupling reaction. Org. Commun. 2018, 11, 2x, 75-79.

156. Hoc, N. T.  Fokin, A. A; Rodionov, V. N. Synthesis of 10-methoxydiamantan-3-one. MOLBANK. 2018, 2, UNSP M990. DOI: 10.3390/M990

154.Yan, H.;Narasimha, K. T.; Denlinger, J.;Li, F. H.;Mo, S.-K.; Nathan Hohman, J.;  Dahl, J. E. P.; ,Carlson, R. M. K.;Tkachenko, B. A.;Fokin, A. A.; Schreiner, P. R.; Hussain, Z.; Shen, Z.-X.; ,Melosh, N. A.Monochromatic photocathodes from graphene-stabilized diamondoids. Nano Lett., 2018, 18, 1099–1103.

153.Yan, H.; Yang, F.; Pan, D.; Lin, Y.; Hohman, J. N.; Solis-Ibarra, D.; Li, F. H.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Galli, G.; Mao, W. L.; Shen Z.-X.; Melosh, N. M. Sterically controlled mechanochemistry under hydrostatic pressure. Nature 2018, 554, 505–510.

152.Gunawan, M. A.; Moncea, O.; Poinsot, D.; Keskes, M.; Domenichini, B.; Heintz, O.; Chassagnon, R.; Herbst, F.; Carlson, R. M. K.; Dahl, J. E. P.; Fokin, A. A.; Schreiner, P. R.; Hierso,  J.-C. Nanodiamond-Palladium Core–Shell Organohybrid Synthesis: A Mild Vapor-Phase Procedure Enabling Nanolayering Metal onto Functionalized sp3-Carbon. Adv. Funct. Mater. 2018, 1705786 (15 p).

151.Gunchenko, P. A.; Li,J.; Liu, B.; Chen, H.; Pashenko, A. P.;Bakhonsky, V. V.; Zhuk. T. S.; Fokin, A. A. Aerobic oxidations with N-hydroxyphthalimide in trifluoroacetic acid. Molec. Cat. 2018, 446, 72-79.

150.Zhyhadlo, Y. Y.; Gaidai, A. V.; Sharapa, D. I.; Mitlenko, A. G.; Shishkin, O. V.; Shishkina, S. V.; Levandovskiy, I. A.; Fokin, A. A. Functionalised Cookson's diketones in chlorosulfonic acid: Towards polysubstituted D3-trishomocubanes. J. Chem. Res. 2017, 41, 12, 677-733.

149.Tyborski, C.; Gillen, R.; Fokin, A. A.; Koso, T. V.; Fokina, N. A.; Hausmann, H.; Rodionov, V. N.; Schreiner, P. R.; Thomsen, C.; Maultzsch, J. Electronic and Vibrational Properties of Diamondoid Oligomers. J. Phys. Chem. 2017, 121, 48, 27082–27088

148.     Fokin, A. A.: Zhuk, T. S.; Blomeyer, S.; Peŕez, C.;  Chernish, L.V.; Pashenko, A. E.; Antony, J.; Vishnevskiy, Y. V.;  Berger, R. J. F.; Grimme, S.; Logemann, C.; Schnell, M.; Mitzel N. W.; Schreiner P. R. Intramolecular London dispersion interaction effects on gas-phase and solid-state structures of diamondoid dimers. J. Amer. Chem. Soc. 2017, 139, 16696-16707.

147.     Tyborski, C.; Meinke, R.; Gillen, R.; Bischoff, T.; Knecht, A.; Richter, R.; Merli, A.; Fokin, A. A.; Koso, T. V.; Rodionov, V. N. Schreiner, P. R.; Moller, T.; Rander, T.; Thomsen, C.; Maultzsch, J. From isolated diamondoids to a van-der-Waals crystal: A theoretical and experimental analysis of a trishomocubane and a diamantane dimer in the gas and solid phase. J. Chem. Phys. 2017, 147, 4, 044303 (6 p.)

146.     Fokin, A. A.; Pashenko, A. E.; Bakhonsky, V. V.; Zhuk. T. S.; Chernish. L. V.; Gunchenko, P. A.; Kushko, A. O.; Becker, J.; Wende, R. C.; Schreiner. P. R. Chiral building blocks based on 1,2-disubstituted diamantanes. Synthesis, 2017. 49, 20032008.

145.     Yan, H.; Hohman, J. N.; Li, F. H.; Jia, C.; Solis-Ibarra, D.; Wu, B.; Dahl, J. E. P.; Carlson, R. M. K.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Vailionis, A.; Kim, T. R.; Devereaux, T. P.; Shen, Z.-X.; Melosh. N. A. Hybrid metal–organic chalcogenide nanowires with electrically conductive inorganic core through diamondoid-directed assembly. Nat. Mater. 2017, 16, 349–355.

144.  Hoc, N. T.;Kushko, A. O.;Fokin, A. A.;Rodionov, V. N. Functional derivatives of diamantanone. Russ. J. Org. Chem. 2016, 52, 8, 1209–1211.

143.Moncea O.; Gunawan, M. A.; Poinsot,D.; Cattey. H.;Becker,J.;Yurchenko,R. I.; Butova,E. D.; Hausmann,H.; Šekutor,M.; Fokin, A. A.; Hierso,J.-C.; Schreiner, P. R. Defying stereotypes with nanodiamonds: Stable primary diamondoid phosphines,  J. Org. Chem. 2016, 81, 8759−8769.

142.     Tverdiy, D. O. Chekanov, M. O.; Savitskiy, P. V.; Syniugin, A. R.; Yarmoliuk, S. M. Fokin, A. A. Efficient preparation of imidazo[1,5-a]pyridine-1-carboxylic acids. Synthesis 2016, 48, A–I.

141.     Ponomarenko, M. V.; Grabowsky,S.; Pal,R.; Röschenthaler, G.-V., Fokin, A. A. SF5-Enolates in Ti(IV)-mediated aldol reactions. J. Org. Chem. 2016, 81, 6783−6791.

140.     Karthik, T. N.; Ge,C.; Fabbri,J. D.; Clay,W.; Tkachenko, B. A.; Fokin, A.A.; Schreiner, P. R.; Dahl, J. E.; Carlson, R. M. K.; Shen, Z. X.; Melosh, N. A. Ultra-low effective work function surfaces using diamondoid monolayers. Nature Nanotech. 2016, 11, 267–273.

139.     Zhang, J. L.; Ishiwata, H.; Babinec, T. M.; Radulaski, M.; Müller, K.; Lagoudakis, K. G.; Dory, C.; Dahl, J.; Edgington, R.; Soulière, V.; Ferro, G.; Fokin, A. A.; Schreiner, P. R.; Shen, Z.-X.; Melosh, N.; Vuckovic, J. Hybrid group IV nanophotonic structures incorporating diamond silicon-vacancy color centers. Nano Lett. 2016, 16, 212−217.

138.Syniugin, A. R.; Chekanov, M. O.; Savitskiy, P. V.; Pashenko, A. E.; Zhuk, T. S.; Yarmoluk, S. M.; Fokin, A A. New method for the synthesis of pyrrolo[2,3-b]dihydroquinolines. Tetrahedron Lett.  2016, 57, 213–215.

137.Valentin, L.; Henss, A.; Tkachenko, B. A.; Fokin, A. A.; Schreiner, P. R.; Becker, S.; Würtele, C.; Schindler, S. Transition metal complexes with cage-opened diamondoid tetracyclo[7.3.1.14,12.02,7]tetradeca-6.11-diene. J. Coor. Chem. 2015, 68, 3295–3301.

136.Lourie, L. F.; Serguchev, Yu. A.; Bentya, A. V.; Ponomarenko, M. V.; Rusanov, E. B.; Vovk, M. V.; Fokin, A. A.; Ignat’ev, N. V. Metal free electrophilic fluoro-cyclization of unsaturated N-hydroxy- and N-acetoxyamides with N–F reagents. J. Fluor. Chem. 2015, 179, 42–47.

135.Bremer, M.; Untenecker, H.; Gunchenko, P. A.; Fokin, A. A.; Schreiner P. R.  Inverted carbon geometries: Challenges to experiment and theory. J. Org. Chem. 2015, 80, 6520−6524.

134.     Zhuk, T. S.; Koso, T.; Pashenko, A. E.; Hoc, N. T.; Rodionov, V. N.; Serafin, M.; Schreiner, P. R.; Fokin, A. A. Toward an understanding of diamond sp2-defects with unsaturated diamondoid oligomer model. J. Am. Chem. Soc. 2015, 137, 6577−6586.

133.     Gunawan, M. A.; Poinsot, D.; Domenichini, B.; Dirand, C.; Chevalier, S.; Fokin, A. A.; Schreiner, P. R.; Hierso, J.-P. The functionalization of nanodiamonds (diamondoids) as a key parameter of their easily controlled self-assembly in micro- and nanocrystals from the vapor phase. Nanoscale, 2015, 7, 1956–1962.

132.     Barabash, A. V.; Didukh, N. A.; Kibal’nyi, N. A.; Butova, E. D.; Schreiner, P. R.;Fokin, A. A. Unusual aerobic oxidation of sterically hindered 1-diamanty methyl ketone. Russ. J. Org. Chem. 2014, 50, 1690–1691.

131.       Gunchenko, P. A.; Novikovskii, A. A.; Byk, M. V.; Fokin, A. A.  Structure and transformations of diamantane radical cation: Theory and experiment. Russ. J. Org. Chem. 2014, 50, 1749–1754.

130.Mishura, A. M.; Sklyarova, A. S.; Shamota, T. V.: Rodionov, V. N.; Fokin, A. A.  Preparative synthesis of pentacyclo[6.3.0.02,6.03,10.05,9]undecan-4-one (D3-Trishomocubanone). Russ. J. Org. Chem. 2014, 50, 1542–1544.

129.Barabash, A. V.; Butova, E. D.; Kanyuk, I. M.; Schreiner, P. R.; Fokin, A. A. Beyond the Corey reaction II: Dimethylenation of sterically congested ketones J. Org. Chem. 2014, 79, 10669−10673. ACS Editor’s Choice, 01.10.2014.

128.Randel, J. C.; Niestemski, F. C.; Botello-Mendez, A. R.; Mar, W.; Ndabashimiye, G.; Melinte, S.; Dahl, J. E. P.; Carlson R. M. K.; Butova, E. D.; Fokin, A. A.; Schreiner, P. R.; Charlier, J.-C.; Manoharan, H. C. Unconventional molecule-resolved current rectification in diamondoid fullerene hybrids. Nature Comm. 2014, 5, 4877 (6 p).

127.Tchernobaev, I. I.; Serguchev, Yu.