Статьи - Sciact

Статьи (41)

#	Публикация
21	Genaev A.M. , Salnikov G.E. , Shernyukov A.V. , Zhu Z. , Koltunov K.Y. Protonation Behavior of 1,1 '-Bi-2-naphthol and Insights into Its Acid-Catalyzed Atropisomerization Organic Letters. 2017. V.19. N3. P.532-535. DOI: 10.1021/acs.orglett.6b03696 WOS Scopus РИНЦ OpenAlex
22	Sokolova A.S. , Yarovaya O.I. , Baev D.S. , Shernyukov A.V. , Shtro A.A. , Zarubaev V.V. , Salakhutdinov N.F. Aliphatic and alicyclic camphor imines as effective inhibitors of influenza virus H1N1 European Journal of Medicinal Chemistry. 2017. V.127. P.661-670. DOI: 10.1016/j.ejmech.2016.10.035 WOS Scopus РИНЦ OpenAlex
23	Lomzov A.A. , Sviridov E.A. , Shernuykov A.V. , Shevelev G.Y. , Pyshnyi D.V. , Bagryanskaya E.G. Study of a DNA Duplex by Nuclear Magnetic Resonance and Molecular Dynamics Simulations. Validation of Pulsed Dipolar Electron Paramagnetic Resonance Distance Measurements Using Triarylmethyl-Based Spin Labels Journal of Physical Chemistry B. 2016. V.120. N23. P.5125-5133. DOI: 10.1021/acs.jpcb.6b03193 WOS Scopus РИНЦ OpenAlex
24	Sokolova A. , Pavlova A. , Komarova N. , Ardashov O. , Shernyukov A. , Gatilov Y. , Yarovaya O. , Tolstikova T. , Salakhutdinov N. Synthesis and analgesic activity of new alpha-truxillic acid derivatives with monoterpenoid fragments Medicinal Chemistry Research. 2016. V.25. N8. P.1608-1615. DOI: 10.1007/s00044-016-1593-z WOS Scopus РИНЦ OpenAlex
25	Shernyukov A.V. , Genaev A.M. , Salnikov G.E. , Rzepa H.S. , Shubin V.G. Noncatalytic Bromination of Benzene: A Combined Computational and Experimental Study Journal of Computational Chemistry. 2016. V.37. N2. P.210-225. DOI: 10.1002/jcc.23985 WOS Scopus РИНЦ OpenAlex
26	Popadyuk I.I. , Markov A.V. , Salomatina O.V. , Logashenko E.B. , Shernyukov A.V. , Zenkova M.A. , Salakhutdinov N.F. Synthesis and biological activity of novel deoxycholic acid derivatives Bioorganic and Medicinal Chemistry. 2015. V.23. N15. P.5022-5034. DOI: 10.1016/j.bmc.2015.05.012 WOS Scopus РИНЦ OpenAlex
27	Sokolova A.S. , Yarovaya O.I. , Shernyukov A.V. , Gatilov Y.V. , Razumova Y.V. , Zarubaev V.V. , Tretiak T.S. , Pokrovsky A.G. , Kiselev O.I. , Salakhutdinov N.F. Discovery of a new class of antiviral compounds: Camphor imine derivatives European Journal of Medicinal Chemistry. 2015. V.105. P.263-273. DOI: 10.1016/j.ejmech.2015.10.010 WOS Scopus РИНЦ OpenAlex
28	Zaytseva E.V. , Shernyukov A.V. , Genaev A.M. , Tamura R. , Grigor'ev I.A. , Mazhukin D.G. New spirocyclic nitroxides of 2,5-dihydroimidazole series flanked by two mesogenic fragments ARKIVOC. 2014. P.10-24. DOI: 10.3998/ark.5550190.p008.808 WOS Scopus РИНЦ OpenAlex
29	Zaitseva E.V. , Shernyukov A.V. , Amitina S.A. , Tamura R. , Grigor'ev I.A. , Mazhukin D.G. Synthesis of Diastereomeric Spirocyclic Nitroxyl Radicals of 3-Imidazoline Series with Two Mesogenic Groups Chemistry of Heterocyclic Compounds. 2014. V.50. N8. P.1113-1125. DOI: 10.1007/s10593-014-1571-7 WOS Scopus РИНЦ OpenAlex
30	Nechepurenko I.V. , Komarova N.I. , Shernyukov A.V. , Vasiliev V.G. , Salakhutdinov N.F. Smiles rearrangements in a series of berberine analogues containing a secondary acetamide fragment Tetrahedron Letters. 2014. V.55. N44. P.6125-6127. DOI: 10.1016/j.tetlet.2014.09.059 WOS Scopus OpenAlex
31	Sokolov D.N. , Rakhmanova M.E. , Luzina O.A. , Shernyukov A.V. , Salakhutdinov N.F. Synthesis of new (+)-usnic acid derivatives with the flavone structure Russian Chemical Bulletin. 2013. V.62. N1. P.212-216. DOI: 10.1007/s11172-013-0031-3 WOS Scopus РИНЦ OpenAlex
32	Shernyukov A.V. , Salakhutdinov N.F. , Tolstikov G.A. Methods of the synthesis of A-seco derivatives of pentacyclic triterpenoids Russian Chemical Bulletin. 2013. V.62. N4. P.878-895. DOI: 10.1007/s11172-013-0120-3 WOS Scopus РИНЦ OpenAlex
33	Шернюков А.В. , Салахутдинов Н.Ф. , Толстиков Г.А. Методы синтеза a-секопроизводных пентациклических тритерпеноидов Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2013. №4. С.880. РИНЦ
34	Соколов Д.Н. , Рахманова М.Е. , Лузина О.А. , Шернюков А.В. , Салахутдинов Н.Ф. Синтез новых производных (+)-усниновой кислоты с флавоновым остовом Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2013. №1. С.211. РИНЦ
35	Shernyukov A.V. , Mainagashev I.Y. , Korchagina D.V. , Genaev A.M. , Komarova N.I. , Salakhutdinov N.F. , Tolstikov G.A. Synthesis of Nitrogen-Containing Derivatives of (18 alpha, 19 beta)-19-Hydroxy-2,3-secooleanane-2,3,28-trioic Acid 28,19-Lactone Helvetica Chimica Acta. 2013. V.96. N9. P.1757-1781. DOI: 10.1002/hlca.201200492 WOS Scopus РИНЦ OpenAlex
36	Sokolova A.S. , Yarovaya O.I. , Shernyukov A.V. , Pokrovsky M.A. , Pokrovsky A.G. , Lavrinenko V.A. , Zarubaev V.V. , Tretiak T.S. , Anfimov P.M. , Kiselev O.I. , Beklemishev A.B. , Salakhutdinov N.F. New quaternary ammonium camphor derivatives and their antiviral activity, genotoxic effects and cytotoxicity Bioorganic and Medicinal Chemistry. 2013. V.21. N21. P.6690-6698. DOI: 10.1016/j.bmc.2013.08.014 WOS Scopus РИНЦ OpenAlex
37	Luzina O.A. , Sokolov D.N. , Shernyukov A.V. , Salakhutdinov N.F. Synthesis of aurones based on usninic acid Chemistry of Natural Compounds. 2012. V.48. N3. P.385-391. DOI: 10.1007/s10600-012-0258-5 WOS Scopus РИНЦ OpenAlex
38	Shernyukov A.V. , Mainagashev I.Y. , Korchagina D.V. , Gatilov Y.V. , Salakhutdinov N.F. , Tolstikov G.A. Preparation and nitration of allobetulin seco-derivatives Chemistry of Natural Compounds. 2012. V.48. N5. P.821-826. DOI: 10.1007/s10600-012-0392-0 WOS Scopus РИНЦ OpenAlex
39	Shernyukov A.V. , Mainagashev I.Y. , Korchagina D.V. , Gatilov Y.V. , Salakhutdinov N.F. , Tolstikov G.A. REDUCTION OF 2,3-Seco-28-OXO-19 beta,28-EPOXY-18 alpha-OLEAN-2,3-DICARBOXYLIC ACID AND ITS CYCLIC ANHYDRIDE Chemistry of Natural Compounds. 2011. V.47. N2. P.237-242. DOI: 10.1007/s10600-011-9891-7 WOS Scopus РИНЦ OpenAlex
40	Shernyukov A.V. , Mainagashev I.Y. , Korchagina D.V. , Gatilov Y.V. , Salakhutdinov N.F. , Tolstikov G.A. Spirocyclization of 2,3-seco-19 beta,28-epoxy-28-oxo-18 alpha-olean-2,3-dicarboxylic anhydride with benzylamines Doklady Chemistry. 2009. V.429. P.286-289. DOI: 10.1134/S0012500809110081 WOS Scopus РИНЦ OpenAlex

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