Personal publications by the year

Personal publicalions (DB NIOCh)

Reviews, articles

1. A.V. Shernyukov, G.E. Salnikov, V.I. Krasnov, A.M. Genaev
   Cluster halogenation of adamantane and its derivatives with bromine and iodine monochloride† Check for updates
   Org. Biomol. Chem., 2022, 20(43), 8515-8527 doi:10.1039/D2OB01455F, IF=3.89
2. N.B. Asanbaeva, A.A. Sukhanov, A.A. Diveikina, O.Y. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, A.G. Maryasov, A.M. Genaev, A.V. Shernyukov, G.E. Salnikov, A.A. Lomzov, D.V. Pyshnyi, E.G. Bagryanskaya
   Application of W-band 19F electron nuclear double resonance (ENDOR) spectroscopy to distance measurement using a trityl spin probe and a fluorine label
   Phys. Chem. Chem. Phys., 2022, 24 (10), 5982-6001 doi:10.1039/D1CP05445G, IF=3.945

Reviews, articles

1. A.V. Shernyukov, G.E. Salnikov, D.A. Rudakov, A.M. Genaev
   The Key Role of Anionic Bromine Clusters Facilitating Br Atom Insertion into the B–H σ-Bond
   Inorganic Chemistry, 2021, 60, 5, 3106-3116 doi:10.1021/acs.inorgchem.0c03392, IF=5.165

Reviews, articles

1. P. Agback, A. Shernyukov, F. Dominguez, T. Agback, E.I. Frolova
   Novel NMR Assignment Strategy Reveals Structural Heterogeneity in Solution of the nsP3 HVD Domain of Venezuelan Equine Encephalitis Virus
   Molecules 2020, 25(24), 5824 doi:10.3390/molecules25245824, IF=3.266
2. T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
   Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
   Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677

Reviews, articles

1. M.A. Bazhenov, A.V. Shernyukov, M.S. Kupryushkin, D.V. Pyshnyi
   Study of the Staudinger Reaction and Reveal of Key Factors Affecting the Efficacy of Automatic Synthesis of Phosphoryl Guanidinic Oligonucleotide Analogs
   Russian Journal of Bioorganic Chemistry, 2019, V. 45, N 6, Pp 699-708 doi:10.1134/S1068162019060074, IF=0.794
2. O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
   Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
   Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59
3. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
   Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
   Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148
4. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
   Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
   Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705
5. A.M. Genaev, L.N. Shchegoleva, G.E. Salnikov, A.V. Shernyukov, L.A. Shundrin, I.K. Shundrina, Z. Zhu, K.Yu. Koltunov
   Acid-Catalyzed vs. Thermally Induced C1-C1' Bond Cleavage in 1,1'-Bi-2-naphthol. An Experimental and Theoretical Study
   J. Org. Chem., 2019, V. 84, N 11, Pp 7238-7243 doi:10.1021/acs.joc.9b00915, IF=4.745
6. A.V. Shernyukov, A.M. Genaev, G.E. Salnikov, V.G. Shubin, H.S. Rzepa
   Elevated reaction order of 1,3,5-tri-tert-butylbenzene bromination as evidence of a clustered polybromide transition state: a combined kinetic and computational study
   Org. Biomol. Chem., 2019, V. 17, N 15, pp 3781-3789 doi:10.1039/C9OB00607A, IF=3.49

Reviews, articles

1. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
   Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
   Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
2. Г.Е. Сальников, А.М. Генаев, А.В. Шернюков, Ч. Чжу, Н.В. Ткаченко, К.Ю. Колтунов
   Конфигурационная стабильность 1,1’-би-2-нафтола в суперкислой среде HSO3F-SBF5-SO2ClF
   Журнал органической химии. 2018. Т. 54. № 5. С. 787-789 (Configurational Stability of 1,1'-Bi-2-naphthol in Superacid System HSO3F-SBF5-SO2ClF/ G. E. Salnikov, A. M. Genaev, A. V. Shernyukov, Z. Zhu, N. V. Tkachenko, K. Yu. Koltunov// Russian Journal of Organic Chemistry, 2018, V. 54, N 5, pp 792-794 doi:10.1134/S1070428018050214), IF=0.655
3. A.M. Genaev, G.E. Salnikov, A.V. Shernyukov, Z. Zhu, K.Yu. Koltunov
   Enhanced enantiostability of BINOL dimethyl ether under moderate acidic conditions
   Mendeleev Communications, 2018, V. 28, N 1, Pp 27-28 doi:10.1016/j.mencom.2018.01.007, IF=2.098

Reviews, articles

1. G.E. Salnikov, A.M. Genaev, A.V. Shernyukov, V.G. Shubin
   Protonation of ninhydrin and indan-1,2,3-trione revisited: A combined theoretical and experimental study
   Journal of Molecular Structure, 2017, V. 1134, Pp 1-5 doi:10.1016/j.molstruc.2016.12.057, IF=1.753
2. K.S. Kovaleva, O.I. Yarovaya, A.V. Shernyukov, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, N.F. Salakhutdinov
   Synthesis of new heterocyclic dehydroabietylamine derivatives and their biological activity
   Chemistry of Heterocyclic Compounds, 2017, V. 53, N 3, pp 364-370 doi:10.1007/s10593-017-2058-0, IF=0.893
3. A.S. Sokolova, О.I. Yarovaya, D.S. Baev, А.V. Shernyukov, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
   Aliphatic and alicyclic camphor imines as effective inhibitors of influenza virus H1N1
   European Journal of Medicinal Chemistry, 2017, V. 127, Pp 661-670 doi:10.1016/j.ejmech.2016.10.035, IF=4.519
4. A.M. Genaev, G.E. Salnikov, A.V. Shernyukov, Z. Zhu, K.Yu. Koltunov
   Protonation Behavior of 1,1'-Bi-2-naphthol and Insights into Its Acid-Catalyzed Atropisomerization
   Org. Lett., 2017, 19 (3), pp 532-535 doi:10.1021/acs.orglett.6b03696, IF=6.578

Reviews, articles

1. A. Sokolova, A. Pavlova, N. Komarova, O. Ardashov, A. Shernyukov, Yu. Gatilov, O. Yarovaya, T. Tolstikova, N. Salakhutdinov
   Synthesis and analgesic activity of new α-truxillic acid derivatives with monoterpenoid fragments
   Medicinal Chemistry Research, 2016, V. 25, N 8, pp 1608-1615 doi:10.1007/s00044-016-1593-z, IF=1.435
2. A.A. Lomzov, E.A. Sviridov, A.V. Shernuykov, G.Yu. Shevelev, D.V. Pyshnyi, E.G. Bagryanskaya
   A Study of a DNA Duplex by Nuclear Magnetic Resonance (NMR) and Molecular Dynamics Simulations. Validation of Pulsed Dipolar Electron Paramagnetic Resonance Distance Measurements using Triarylmethyl-Based Spin Labels
   J. Phys. Chem. B, 2016, 120 (23), pp 5125-5133 doi:10.1021/acs.jpcb.6b03193, IF=3.187
3. A.V. Shernyukov, A.M. Genaev, G.E. Salnikov, H.S. Rzepa, V.G. Shubin
   Noncatalytic bromination of benzene: A combined computational and experimental study
   Journal of Computational Chemistry, V. 37, N 2, 15 January 2016, Pp 210-225 doi:10.1002/jcc.23985, IF=3.648

Reviews, articles

1. A.S. Sokolova, О.I. Yarovaya, А.V. Shernyukov, Yu.V. Gatilov, Yu.V. Razumova, V.V. Zarubaev, T.S. Tretiak, А.G. Pokrovsky, O.I. Kiselev, N.F. Salakhutdinov
   Discovery of a new class of antiviral compounds: Camphor imine derivatives
   European Journal of Medicinal Chemistry, V. 105, 13 November 2015, Pp 263-273 doi:10.1016/j.ejmech.2015.10.010, IF=3.447
2. I.I. Popadyuk, A.V. Markov, O.V. Salomatina, E.B. Logashenko, A.V. Shernyukov, M.A. Zenkova, N.F. Salakhutdinov
   Synthesis and biological activity of novel deoxycholic acid derivatives
   Bioorganic & Medicinal Chemistry, V. 23, N 15, 2015, Pp 5022-5034 doi:10.1016/j.bmc.2015.05.012, IF=2.792

Reviews, articles

1. E.V. Zaytseva, A.V. Shernyukov, A.M. Genaev, R. Tamura, I.A. Grigor’ev, D.G. Mazhukin
   New spirocyclic nitroxides of 2,5-dihydroimidazole series flanked by two mesogenic fragments
   ARKIVOC, 2014, (vi) 10-24. http://www.arkat-usa.org/get-file/51547/ doi:10.3998/ark.5550190.p008.808, IF=1.75
2. I.V. Nechepurenko, N.I. Komarova, A.V. Shernyukov, V.G. Vasiliev, N.F. Salakhutdinov
   Smiles rearrangements in a series of berberine analogues containing a secondary acetamide fragment
   Tetrahedron Letters, V. 55, N 44, 29 October 2014, Pages 6125-6127. doi:10.1016/j.tetlet.2014.09.059, IF=2.391
3. E.V. Zaitseva, A.V. Shernyukov, S.A. Amitina, R. Tamura, I.A. Grigor’ev, D.G. Mazhukin
   Synthesis of Diastereomeric Spirocyclic Nitroxyl Radicals of 3-Imidazoline Series with Two Mesogenic Groups
   Chemistry of Heterocyclic Compounds, November 2014, V. 50, N 8, pp 1113-1125. doi:10.1007/s10593-014-1571-7, IF=0.698

Reviews, articles

1. A.S. Sokolova, О. I. Yarovaya, А.V. Shernyukov, М.A. Pokrovsky, А.G. Pokrovsky, V.A. Lavrinenko, V.V. Zarubaev, T.S. Tretiak, P.M. Anfimov, O.I. Kiselev, A.B. Beklemishev, N.F. Salakhutdinov
   New quaternary ammonium camphor derivatives and their antiviral activity, genotoxic effects and cytotoxicity
   Bioorganic & Medicinal Chemistry, 2013, V. 21, N 21, P: 6690-6698. doi:10.1016/j.bmc.2013.08.014, IF=2.903
2. A. V. Shernyukov, I.Ya. Mainagashev, D. V. Korchagina, A. M. Genaev, N. I. Komarova, N. F. Salakhutdinov, G. A. Tolstikov
   Synthesis of Nitrogen-Containing Derivatives of (18α,19β)-19-Hydroxy-2,3-secooleanane-2,3,28-trioic Acid 28,19-Lactone
   Helvetica Chimica Acta, 2013, V. 96, N 9, P. 1757-1781. doi:10.1002/hlca.201200492, IF=1.383
3. А. В. Шернюков, Н. Ф. Салахутдинов, Г. А. Толстиков
   Методы синтеза A секопроизводных пентациклических тритерпеноидов
   Известия АН. Серия химическая, 2013, N 4, С. 880-896. (Methods of the synthesis of A-seco derivatives of pentacyclic triterpenoids/ A. V. Shernyukov, N. F. Salakhutdinov, G. A. Tolstikov// Russian Chemical Bulletin, 2013, V. 62, N 4, pp 878-895. doi:10.1007/s11172-013-0120-3), IF=0.423
4. Д.Н. Соколов, М.Е. Рахманова, О.А. Лузина, А.В. Шернюков, Н.Ф. Салахутдинов
   Синтез новых производных (+)-усниновой кислоты с флавоновым остовом
   Известия АН. Серия химическая, 2013, N 1, С. 211–215. (Synthesis of new (+)-usnic acid derivatives with the flavone structure/ D. N. Sokolov, M. E. Rakhmanova, O. A. Luzina, A. V. Shernyukov, N. F. Salakhutdinov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 212-216 doi:10.1007/s11172-013-0031-3), IF=0.423

Reviews, articles

1. A.V. Shernyukov, I.Ya. Mainagashev, D.V. Korchagina, Yu.V. Gatilov, N.F. Salakhutdinov, G.A. Tolstikov
   Preparation and nitration of allobetulin seco-derivatives
   Chem. Nat. Compd., 2012, V. 48, N 5, pp. 821-826. doi:10.1007/s10600-012-0392-0, IF=1.29
2. O.A. Luzina, D.N. Sokolov, A.V. Shernyukov, N.F. Salakhutdinov
   Synthesis of aurones based on usninic acid
   Chem. Nat. Compd., 2012, V. 48, N 3, pp. 385-391. doi:10.1007/s10600-012-0258-5, IF=1.29

Reviews, articles

1. A.V. Shernyukov, I.Y. Mainagashev, D.V. Korchagina, Y.V. Gatilov, N.F. Salakhutdinov, G.A. Tolstikov
   Reduction of 2,3-seco-28-oxo-19β,28-epoxy-18α-olean-2,3- dicarboxylic acid and its cyclic anhydride
   Chem. Nat. Compd., 2011, V. 47, N 2, pp 237-242. doi:10.1007/s10600-011-9891-7, IF=0.693

Reviews, articles

1. А.В. Шернюков, А.Я. Майганашев, Д.В. Корчагина, Ю.В. Гатилов, Н.Ф. Салахутдинов, Г.А. Толстиков
   Спироциклизация 2,3-секо-28-оксо-19b,28-эпокси-18a-олеан-2,3-ангидрида с бензиламинами
   Доклады Академии наук (Химия), 2009, т.429, №3, C.339-342. (Spirocyclization of 2,3-seco-19 beta,28-epoxy-28-oxo-18 alpha-olean-2,3-dicarboxylic anhydride with benzylamines/ A.V. Shernyukov, I.Ya. Mainagashev, D.V. Korchagina, Yu.V. Gatilov, N.F. Salakhutdinov, G.A. Tolstikov// Doklady Chemistry, 2009, V.429,N 1, pp 286-289 doi:10.1134/S0012500809110081), IF=0.231