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

 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.

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.

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.

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.

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.

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

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

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.

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

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

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

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.

13.    Shubina, T. E.; Fokin, A. A. Hydrocarbon σ-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.

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.

 

B) Статті в журналах

 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.

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

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

 4.      Krasutsky, P. A.; Fokin, A. A.; Yurchenko, A. G. The synthesis and reactivity of 3-methylene-7-vinylidenobicyclo[3.3.1]nonane. Zhurnal Organ. Khimii1985, 21, 2522–2626.

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

 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. Zhurnal Organ. Khimii 1986, 22, 460–461.

 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. Zhurnal.Organ. Khimii 1990, 26, 1016–1024.

 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.

 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.

 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.  Zhurnal Organ. Khimii 1991, 27, 992–999.

 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. Zhurnal Organ. Khimii 1991, 27, 1363.

 12.  Krasutsky, P. A.; Fokin, A. A.; Baula, O. P.; Kulik, N. I.; Yurchenko, A. G.  The structure of the stereoisomeric monochlorochrysanthemic acids. Zhurnal Organ. Khimii. 1991, 27, 1279–1283.

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

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.

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

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. Zhurnal Org. Khimii 1992, 28, 1098–1099.

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.

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

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. Zhurnal Org. Khimii 1994, 30, 669–679.

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. Zhurnal Org. Khimii 1994, 30, 940–941.

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.

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). Zhurnal Org. Khimii 1995, 31, 796–797.

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.

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.

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.

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.

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.

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.  Zhurnal Org. Khimii. 1998, 34, 776–777.

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.

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.

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.

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.

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

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.

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.

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. Lett2000, 2201–2204.

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.

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.

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.

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.

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

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.

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.

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.

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.

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

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.

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.

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.

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.

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.

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.

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.

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.

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.

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

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.

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.

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.

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

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.

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 Institut2005, 1, 107–115.

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.

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.

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.

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.

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.

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.

69.   Ponomarenko, M. V.; Serguchev Y. A.; Ponomarenko, B. V.; Roschenthaler, 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.

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.

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.

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.

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.

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

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.

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.

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

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.

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.

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.

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.

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.

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.

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.

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

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.

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.

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.

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). Zhurn. Org. Khim. 2009, 45, 11, 1644−1647. 

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.

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.

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.

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

94.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.

95.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).

96.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).

97.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.

98.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.

99.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. 

100.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. 

101.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. 

102.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.

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

104.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. Zhurn. Org. Khim. 2011, 47, 1293–1299. 

105.Schreiner, P. R.; Chernish, L. V.; Gunchenko, P. A.; Tikhonchuk, E. Yu.; Heike, 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 and Engineering News 2011 September, 13, 55.

106.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.

107.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.

108.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

109.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.

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

111. 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.

112. 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.

 113. 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.

114. 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 photoelectronspectroscopy. J. Chem. Phys. 2013, 139, 084310 (6 p).

 115. 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.

 116. 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). Cent. Eur. J. Chem. 2013, 11, 2144–2150.

 117. 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.

 118. 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. 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, and S. M. Design, synthesis and biological evaluation of 2-aminopyrimidinonesand their 6-aza-analogs as a new class of СК2 inhibitors. J. Enz. Inhib. Med. Chem.2014, 29, 5, 639­–646.

 119. 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. 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. 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. 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. 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. Ponomarenko, M. V.; Serguchev, Yu. A.; Hirschberg, M. E.; Röschenthaler, G.-V.; Fokin, A. A. Elemental F2with transannular dienes: Regioselectivities andmechanisms. Chem. Eur. J. 2014, 20, 10383–10391.

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

 128. 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. 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. 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. 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 easilycontrolled self-assembly in micro- and nanocrystals from the vapor phase.Nanoscale, 2015, 7, 1956–1962.

132.    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.    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.    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.    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. 201568, 3295–3301.

136.    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.  201657, 213–215.

137.    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.

 

 

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.

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