Publications

Gram-Scale Synthesis of Amines Bearing a gem-Difluorocyclopropane Moiety
P. S. Nosik, A. O. Gerasov, R. O. Boiko, E. Rusanov, S. V. Ryabukhin, O. O. Grygorenko, D. M. Volochnyuk
Adv. Synth. Catal.359 (2017), 3126-3136. DOI: 10.1002/adsc.201700857
Graphical abstract - Synthesis of Amines Bearing a gem-Difluorocyclopropane Moiety - Life Chemicals


Conformational structure of the unsymmetrical monomethine cyanine bearing 2-azaazulene and 2-benzothiazole residues as terminal groups: Experimental and quantum-chemical investigation
A.B. Ryabitskii, J.L. Bricks, A.D. Kachkovskii, A.N. Chernega, Y.G. Vlasenko
J. Mol. Str. 982 (2010) 79. https://doi.org/10.1016/j.molstruc.2010.08.010

One-pot synthesis of diethyl 4,4’-(1,4-phenylene)bis-[6-(halomethyl)-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylates] and their bispyrrolocyclization
I.O. Lebedyeva, M.V. Povstyanoy, V.M. Povstyanoy, O.G. Panasyuk, E.S. Guban’, A.B. Ryabitskii
Monatsh. Chem. 141 (2010) 997–1000. DOI 10.1007/s00706-010-0354-9
Graphical abstract - One-pot synthesis of diethyl 4,4’-(1,4-phenylene)bis-[6-(halomethyl)-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylates] and their bispyrrolocyclization - Life Chemicals

Studies of 2‐Azaazulenium Derivatives: The Natures of Electron Transitions in the 2‐Azaazulenium Cation and in Monomethine Cyanine Dyes Bearing 2‐Azaazulenium Moieties as Terminal Groups
Julia Bricks, Aeksey Rabitskii, and Alexei Kachkovskii
Chem. Eur. J. v. 16, 29 (2010) 8773-8784. DOI 10.1002/chem.201000366

Ternary Condensation of Biginelli Thiones, Chloroacetic Acid, and Aldehydes as an Effective Approach towards Thiazolo[3,2-a]pyrimidines and 5-Arylidenethiazolidine-2,4-diones
Iryna O. Lebedyeva, Mykhaylo V. Povstyanoy, Aleksey B. Ryabitskii, and Vyacheslav M. Povstyanoy
J. Heterocyclic Chem. 47 (2010) 368. DOI 10.1002/jhet.323
Graphical abstract - Effective Approach towards Thiazolo[3,2-a]pyrimidines and 5-Arylidenethiazolidine-2,4-diones - Life Chemicals

Interaction of 4-substituted 5-carbethoxy-6-chloromethylpyrimidin-2-one with hydrazines and hydrazide derivatives: synthesis and structure
I.O. Lebedyeva, M.V. Povstyanoy, A.B. Ryabitsky, and O.G. Panasyuk
Ukr. Khim. Zhur. 76 (2010) 46.

Octafluoro-4,40-bipyridine and its derivatives: Synthesis, molecular and crystal structure
Alexey V. Gutov , Eduard B. Rusanov, Alexey B. Ryabitskii, Alexander N. Chernega
J. Fluor. Chem. 131 (2010) 278–281. DOI: 10.1016/j.jfluchem.2009.11.022
Graphical abstract - Octafluoro-4,40-bipyridine and its derivatives: Synthesis, molecular and crystal structure - Life Chemicals

Crystalline and Molecular Design of Functionalized Viologens
A. V. Gutov, E. B. Rusanov, A. B. Ryabitskii, I. F. Tsimbal, and A. N. Chernega
Russ. J. General Chem. v. 79, 9 (2009) 1910. DOI: 10.1134/S1070363209090175

Studies of 2-Azaazulenium Derivatives: The Natures of Electron Transitions in the 2-Azaazulenium Cation and in Monomethine Cyanine Dyes Bearing 2-Azaazulenium Moieties as Terminal Groups
Julia Bricks, Aleksey Ryabitskii, and Alexei Kachkovskii
Eur. J. Org. Chem. (2009) 3439. DOI: 10.1002/ejoc.200900204

3-aminopyrrole-2,5-diones 3*. Synthesis of benzenehexa-carboxylic acid trimethylimide and 1,1′-dimethyl-4-methylamino-[3,3′]bipyrrolyl-2,5,2′,5′-tetraone by the reaction of 1-methyl-3-methylaminopyrrole-2,5-dione with hydrogen chloride
S. V. Chepyshev, Yu. N. Chepysheva, A. B. Ryabitsky, and A. V. Prosyanik Chem. Het. Comp. v. 45, 7 (2009) 823. DOI: 10.1007/s10593-009-0355-y

2-Aminopyrrole-2,5-diones 2. Vinyl nucleophilic substitution of the alkylamino group in 1-alkyl-3-alkylaminopyrrole-2,5-diones by arylamines
S. V. Chepyshev, Yu. N. Chepysheva, A. B. Ryabitskii, and A. V. Prosyanik
Chem. Het. Comp. v. 44, 5 (2008) 523. DOI: 10.1007/s10593-008-0071-z