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?2023 §Ô§à§Õ
M. A. Kushner, T. S. Seliverstova, L. G. Matusevich. Acid Hydrolysis of Glycosyl¨CGlycose Bond Disaccharides in Water¨COrganic Media. Russian Journal of Physical Chemistry A, 2023, Vol. 97, No. 3, pp. 455¨C460. DOI: 10.1134/S0036024423030160
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2022 §Ô§à§Õ
1. Synthesis of 1,2,6-trisubstituted indoles from 6-pro-pargylcyclohex-2-enones and primary amine. / S. G. Mikhalyonok, N. M. Kuz¡¯menok, V. S. Bezborodov, A. S. Arol // Chemistry of Heterocyclic Compounds. 2022. ¨C V. 58, ¡í (4¨C5). ¨C P. 217¨C226.2.An original approach to creating liquid crystals and anisotropic materials with a wide range of practical application / V. Bezborodov, S. Mikhalyonok, N. Kuz¡¯menok, V. Lapanik, R. Talroze // SID Symposium Digest of Technical Papers. October 2022. 53(S1):545-545. DOI: 10.1002/sdtp.16018.
3. Chemo- and regioselective oxidation of substituted 2,3,4,9-tetrahydro-1H-carbazoles / Mikhalyonok, S.G., Savelyev, A.I., Kuz¡¯menok, N.M., Bezborodov V.S. // Chem. Heterocycl. Comp. ¨C 2022. ¨C Vol. 58, P. 403¨C411.
4.The role of terphenyl-containing carboxylic acid in the oligomerization of aryl vinyl ketone /G.N. Bondarenko, O.N. Karpov, G.A. Shandryuk, A. V. Finko, Y.I. Derikov, S.G. Mikhalyonok, V.S. Bezborodov, R.V. Talroze // Physical Chemistry Chemical Physics. ¨C 2022. ¨C Vol. 24, ¡í 42. ¨C P. 26083¨C26093. DOI:10.1039/D2CP03187F.
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2021 §Ô§à§Õ
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2020 §Ô§à§Õ
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2.?Seliverstova, T.S.,?Kushner, M.A.,?Matusevich, L.G.?Kinetics and Mechanism of the Hydrolysis of Benzyl Ether Bonds in Aqueous¨COrganic Media.?Russ. J. Phys. Chem.?94,?310¨C316 (2020). https://doi.org/10.1134/S0036024420020302?(Impact Factor: 0.581).
3. Tiago A. Fernandes, Vania Andre, Aliaksandr Arol, Angela Franca,?Sergei Mikhalyonok,?Nuno Cerca, Alexander M. Kirillov, New Silver (Thio)Semicarbazide Derivatives: Synthesis, Structural Features, and Antimicrobial Activity, New Journal of Chemistry, 2020, 44, 10924-10932. (http://dx.doi.org/10.1039/D0NJ02013C)
4.?§´. §³. §³§Ö§Ý§Ú§Ó§Ö§â§ã§ä§à§Ó§Ñ, §®. §¡. §¬§å§ê§ß§Ö§â, §. §¤.?§®§Ñ§ä§å§ã§Ö§Ó§Ú§é. §¬§Ú§ß§Ö§ä§Ú§Ü§Ñ §Ú §Þ§Ö§ç§Ñ§ß§Ú§Ù§Þ §â§Ö§Ñ§Ü§è§Ú§Û §Ô§Ú§Õ§â§à§Ý§Ú§Ù§Ñ §Ò§Ö§ß§Ù§Ú§Ý§ï§æ§Ú§â§ß§í§ç §ã§Ó§ñ§Ù§Ö§Û §Ó §Ó§à§Õ§ß§à-§à§â§Ô§Ñ§ß§Ú§é§Ö§ã§Ü§Ú§ç §ã§â§Ö§Õ§Ñ§ç / §¨§å§â§ß§Ñ§Ý §æ§Ú§Ù§Ú§é§Ö§ã§Ü§à§Û §ç§Ú§Þ§Ú§Ú, 2020, T. 94, ¡í 2, §ã§ä§â. 230-237.(https://doi.org/10.31857/S0044453720020314)
5.?§¬§å§ê§ß§Ö§â §®.§¡., §³§Ö§Ý§Ú§Ó§Ö§â§ã§ä§à§Ó§Ñ §´.§³.?§²§Ñ§Ù§â§Ñ§Ò§à§ä§Ü§Ñ §á§à§Õ§ç§à§Õ§à§Ó §Ü §Ü§à§Þ§á§Ý§Ö§Ü§ã§ß§à§Û §á§Ö§â§Ö§â§Ñ§Ò§à§ä§Ü§Ö §Ú §å§ä§Ú§Ý§Ú§Ù§Ñ§è§Ú§Ú §Ü§à§â§í §à§Ý§î§ç§Ú / §·§Ú§Þ§Ú§ñ §â§Ñ§ã§ä§Ú§ä§Ö§Ý§î§ß§à§Ô§à §ã§í§â§î§ñ, 2020, ¡í3. §³. 171-178. (https://doi.org/10.14258/jcprm.2020036548)
6. §¨. §£. §ª§Ô§ß§Ñ§ä§à§Ó§Ú§é, §¡. §. §¦§â§Þ§à§Ý§Ú§ß§ã§Ü§Ñ§ñ, §£. §¤. §±§Ö§ä§å§ê§à§Ü,?§Á. §®. §¬§Ñ§ä§à§Ü, §¦. §£. §¬§à§â§à§Ý§Ö§Ó§Ñ. §³§Ú§ß§ä§Ö§Ù 2-§Ñ§â§Ú§Ý§Ñ§Þ§Ú§ß§à§á§Ú§â§Ú§Þ§Ú§Õ§Ú§ß§à§Ó§í§ç §Ñ§Þ§Ú§Õ§à§Ó §Ú §ã§å§Ý§î§æ§Ñ§Þ§Ú§Õ§à§Ó 4,4'-§à§Ü§ã§Ú§Õ§Ú§Ò§Ö§ß§Ù§à§Û§ß§à§Û §Ü§Ú§ã§Ý§à§ä§í / §¨§å§â§ß§Ñ§Ý §à§â§Ô§Ñ§ß§Ú§é§Ö§ã§Ü§à§Û §ç§Ú§Þ§Ú§Ú, 2020, §ä§à§Þ 56, ¡í 12, §ã. 1869¨C1876. (https://doi.org/10.31857/S0514749220120071)
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