Division of Functional Materials Chemistry
State Scientific Institution “Institute for Single Crystals”
of National Academy of Sciences of Ukraine

Main menu

Selected publications

Books

  1. V.A. Chebanov, S.M. Desenko, T.W. Gurley. Azaheterocycles Based on α,β-Unsaturated Carbonyls, Springer, 2008, 212 p.

  2. V.A. Chebanov, K.A. Gura, S.M. Desenko. Aminoazoles as Key Reagents in Multicomponent Heterocyclizations // in book Topics in Heterocyclic Chemistry, Springer, 2010, Vol. 23, p. 41–84.

  3. Chebanov V.A., Gorobets N.Yu., Sedash Yu.V. Third Component 1,3-Dicarbonyl compound (with Ureas: Biginelli Reaction). In book: Multicomponent Reactions 1. General Discussion and Reactions Involving a Carbonyl Compound as Electrophilic Component (Ed.: T.J.J. Müller). Science of Synthesis Series, Georg Thieme Verlag KG, Stuttgart, 2014, 29-66.

  4. Zbruyev O.I., Pinchukova N.O., Saraev V.E., Myasnikova D.Yu., Valsenko G.S., Shlyapkina Yu.V., Evtushenko E.V., Chebanov V.A. Supramolecular complex of 1-methylcycloprepene with cucurbit[6]uril as an effective means for apples treatment. In book: Novel functional substances and materials of chemical industry, Akademperiodika, Kyiv, 2021, 26-38 (book chapter, in Ukrainian).

  5. Chebanov V.A., Desenko S.M., Lipson V.V., Gorobets N.Yu. Multicomponent-Switched Reactions in Synthesis of Heterocycles. In book: Multicomponent Reactions towards Heterocycles: Concepts and Applications (Eds.: Erik Van der Eycken, Upendra K. Sharma), Wiley-VCH, Weinheim, Germany 2022, 287-338.

Reviews

  1. Chebanov V.A., Desenko S.M. Multicomponent heterocyclization reactions with controlled selectivity, Chem. Heterocycl. Comp., 2012, 48, 566-583.

  2. Chebanov V.A., Desenko S.M. Switchable multicomponent heterocyclization for diversity oriented synthesis, Diversity Oriented Synthesis, 2014, 1, 43-63.

  3. Tkachenko V.V., Chebanov V.A. Reactions of 3(5)-Aminoizoxazoles using Classical Methods of Activation, Microwave Irradiation, and Ultrasonication, Chem. Heterocycl. Comp., 2016, 52, 11, 866-886.

  4. Sharma P.P., Rathi B., Rodrigues J., Gorobets N.Yu. Self-Assembled Peptide Nanoarchitectures: Applications and Future Aspects, Curr. Top. Med. Chem., 2015, 15, 1268-1289.

  5. Pavlovska T.L., Redkin R.G., Lipson V.V., Atamanuk D.V. Molecular diversity of spirooxindoles. Synthesis and biological activity, Mol. Div., 2016, 299-344.

  6. Murlykina M.V., Morozova A.D., Zviagin I.M., Sakhno Ya.I., Desenko S.M., Chebanov V.A. Amonoazole-Based Diversity-Oriented Synthesis of Heterocycles, Front. Chem., 2018, 6, article 527, 1-43.

Original articles

  1. Murlykina M.V., Sakhno Ya.I., Desenko S.M., Shishkina S.V., Shishkin O.V., Sysoiev D.O., Kornet M.N., Schlos D., Goeman J.L., Van der Eycken J., Van der Eycken E.V., Chebanov V.A. Study of Chemoselectivity of Multicomponent Heterocyclization Involving 3-Fmino-1,2,4-triazole and Pyruvic Acid as Key Reagents and Biological Activity of the Reaction Products, Eur. J. Org. Chem., 2015, 4481-4492.

  2. Ziolkovskiy D.V., Lipson V.V., Nikitina A.D., Chebanov V.A. Substituted 1,2,4-oxodiazoles as Potent Inhibitors of Human 11β-Hydroxysteroid Dehydrogenase Type 1 (11β-HSD1): Virtual Screening and Docking Results, Lett. Drug Des. Discov., 2016, 13(3), 226-233.

  3. Murlykina M.V., Kornet M.N., Desenko S.M., Shishkina S.V., Shishkin O.V., Brazhko A.A., Musatov V.I., Van der Eycken E.V., Chebanov V.A. New tricks of well-known aminoazoles in isocyanide-based multicomponent reactions and antibacterial study of the compounds synthesized, Beilstein J. Org. Chem., 2017, 13, 1050-1063.

  4. Pinchukova N.A., Voloshko A.Yu., Merko M.A., Bondarenko Ya.A., Chebanov V.A. Intensification of ion exchange desoption of thiamine diphosphate by low-powered ultrasound, Ultrason. Sonochem., 2018, 41, 261-266.

  5. Zhikol, O.A., Shishkina, S.V., Lipson, V.V., Semenenko, A.N., Mazepa, A.V., Borisov, A.V. and Mateychenko, P.V., Low molecular weight supramolecular dehydro- epiandrosterone-based gelators: synthesis and molecular modeling study, NJC, 2019, 43 (33), 13112-13121.

  6. Zviagin E., Saraev V., Sysoiev D., Klepetářová D., Mazur M., Zhelavskyi O., Shliapkina Yu., Müller Th.J.J., Chebanov V. Synthesis of 1-(3-(1-substituted-1,2,3-triazol-4-yl)- 1,2,4-triazol-5-yl)-tetrazoles by Sequential Assembly of Azole Fragments, ChemistrySelect, 2021, 6, 12890-12894.

  7. Mazur M.O., Zhelavskyi O.S., Zviagin E.M., Shishkina S.V., Musatov V.I., Kolosov M.A., Shvets E.H., Andryushchenko A.Yu., Chebanov V.A. Effective microwave-assisted approach to 1,2,3-triazolobenzodiazepinones via tandem Ugi-reaction / catalyst-free intramolecular azide-alkyne cycloaddition, Beilstein J. Org. Chem., 2021, 17, 678-687.

  8. Miasnikova D.Yu., Pinchukova N.A., Saraev V.E., Musatov V.I., Vlasenko A.S., Shliapkina Yu.V., Zbruyev O.I., Chebanov V.A. Chemical Modification and Quantification of 1-Methylcyclopropene in Supramolecular Complex with Cucurbit[6]uril by High Performance Liquid Chromatography, Chromatographia, 2022, 85, 1009-1016.

  9. Doğan I.S., Gümüs M.K., Gorobets N.Yu., Reis R., Orak D., Sipahi H., Sari S., Chebanov V.A. In Vitro Cytotoxicity of Methano[1,2,4]Triazolo[1,5-c][1,3,5]Benzoxadiazocine Derivatives and Their Effects on Nitrite and Prostaglandin E2 (PGE2) Levels, Pharm. Chem. J., 2022, 56, 769-776.

  10. Zbryuev O.I., Belikov K.N., Khimchenko S.V., Blank T.A. Chebanov V.A. Modified Greener Procedure for the Synthesis of Cucurbit[6]uril, Org. Process Res. Dev., 2023, 27, 1, 129-135.

  11. Sakhno Ya.I., Radchenko O.V., Saraev V.E., Shliapkina Yu.V., Kaidash M.B., Shyshkina M.O., Shishkina S.V., Musatov V.I., Desenko S.M., Chebanov V.A. Temperature Controlled Diastereoselective Doebner/Ugi Tandem Reaction, SynOpen, 2023, 7, 258-266.

  12. Kolomiiets O.V., Tsygankov A.V., Kornet M.N., Brazhko A.A., Musatov V.I., Chebanov V.A. Synthesis of imidazo[1,2-a]pyridine-containing peptidomimetics by tandem of Groebke-Blackburn-Bienaymé and Ugi reactions, Beilstein J. Org. Chem., 2023, 19, 727-735.