Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН
- 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
- L.S. Konstantinova, I.V. Baranovsky, E.A. Pritchina, M.S. Mikhailov, I.Yu. Bagryanskaya, N.A. Semenov, I.G. Irtegova, G.E. Salnikov, K.A. Lyssenko, N.P. Gritsan, A.V. Zibarev, O.A. Rakitin
Fused 1,2,3-Thiaselenazoles Synthesized from 1,2,3-Dithiazoles through Selective Chalcogen Exchange
Chemistry - A European Journal, 2017, V. 23, N 67, Pp 17037-17047 doi:10.1002/chem.201703182, IF=5.316
- N.A. Pushkarevsky, P. A. Petrov, D.S. Grigoriev, A.I. Smolentsev, L.M. Lee, F. Kleemiss, G.E. Salnikov, S.N. Konchenko, I. Vargas-Baca, S. Grabowsky, J. Beckmann, A.V. Zibarev
Nature of Bonding in Donor-Acceptor Interactions Exemplified by Complexes of N-Heterocyclic Carbenes with 1,2,5-Telluradiazoles
Chemistry - A European Journal, 2017, V. 23, N 46, Pp 10987-10991 doi:10.1002/chem.201703018, IF=5.316
- 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
- N. Pushkarevsky, E. Chulanova, L. Shundrin, A. Smolentsev, G. Salnikov, E. Pritchina, A. Genaev, I. Irtegova, I. Bagryanskaya, S. Konchenko, N. Gritsan, J. Beckmann, A. Zibarev
Radical Anions, Radical-Anion Salts and Anionic Complexes of 2,1,3-Benzochalcogenadiazoles (S, Se, Te)
Chemistry - A European Journal, Chemistry - A European Journal, 2019, V. 25, N 3, Pp 806-816 doi:10.1002/chem.201803465, IF=5.16
- N.A. Semenov, D.E. Gorbunov, M.V. Shakhova, G.E. Salnikov, I.Yu. Bagryanskaya, V.V. Korolev, J. Beckmann, N.P. Gritsan, A.V. Zibarev
Donor-Acceptor Complexes between 1,2,5-Chalcogenadiazoles (Te, Se, S) and the Pseudo Halides CN- and XCN- (X = O, S, Se, Te)
Chemistry - A European Journal, 2018, V.24, N 49, Pp 12983-12991 doi:10.1002/chem.201802257, IF=5.16
- S.A. Dobrynin, Yu.I. Glazachev, Yu.V. Gatilov, E.I. Chernyak, G.E. Salnikov, I.A. Kirilyuk
Synthesis of 3,4-Bis-(hydroxymethyl)-2,2,5,5-tetraethylpyrrolidin-1-oxyl via 1,3-Dipolar Cycloaddition of Azomethine Ylide to Activated Alkene
J. Org. Chem., 2018, V. 83, N 10, Pp 5392-5397 doi:10.1021/acs.joc.8b00085, IF=4.805
- 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
- S.F. Vasilevsky, T.F. Mikhailovskaya, G.E. Salnikov, V.I. Mamatyuk, G.A. Bogdanchikov, M. Manoharan, I.V. Alabugin
Competition between 5-Exo and 6-Endo-dig Anionic Cyclizations of Hydrazides of o-Acetylenyl Benzoic Acids and Based-catalyzed Fragmentation/Recyclization of the Initial 5-Exo-Dig Products.
J. Org. Chem. 2009, V. 74, N 21, pp 8106-8117. doi:10.1021/jo901551g, IF=3.951
- 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
- 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
- A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
DFT insights into superelectrophilic activation of α,β-unsaturated nitriles and ketones in superacids
Org. Biomol. Chem., 2022,20(34), 6799-6808 doi:10.1039/D2OB01141G, IF=3.89
- A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
Unusual temperature-sensitive protonation behaviour of 4-(dimethylamino)pyridine
Org. Biomol. Chem., 2021, V. 19, N 4, Pp 866-872 doi:10.1039/D0OB01893G, IF=3.876
- O.V. Ardashov, A.V. Pavlova, A.K. Mahato, Yu. Sidorova, E.A. Morozova, D.V. Korchagina, G.E. Salnikov, A.M. Genaev, O.S. Patrusheva, N. Li-Zhulanov, T.G. Tolstikova, K.P. Volcho, N. Salakhutdinov
A novel small molecule supports the survival of cultured dopamine neurons and may restore the dopaminergic innervation of the brain in the MPTP mouse model of Parkinson's disease
ACS Chemical Neuroscience, 2019, V. 10, N 10, Pp 4337-4349 doi:10.1021/acschemneuro.9b00396, IF=3.861
- G. E. Salnikov, A. M. Genaev, V. A. Bushmelev, A. A. Nefedov, V. G. Shubin
Formation of dications bearing a S(OH)2+ group from long-lived 9,9-dimethyl-10 R-phenanthrenium cations in FSO3H–SbF5/SO2ClF/SO2: a mechanistic study
RSC Advances, 2014, V. 4, N 95, 52831-52835. doi:10.1039/C4RA11673A, IF=3.707
- G.E. Salnikov, A.M. Genaev, V.G. Vasiliev, V.G. Shubin
Interaction of acetonitrile with trifluoromethanesulfonic acid: unexpected formation of a wide variety of structures
Org. Biomol. Chem., 2012, V.10, N 11, 2282-2288. doi:10.1039/c2ob06841a, IF=3.696
- 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
- G.E. Salnikov, A.M. Genaev, V.A. Bushmelev, V.G. Shubin
Migration of methylethynyl group in a long-lived carbocation
Organic & Biomolecular Chemistry, 2013, V. 11, N 9, P. 1498-1501. doi:10.1039/c2ob27208c, IF=3.568
- Z. Zhu, A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
Mechanistic investigation of superelectrophilic activation of 1,1'-bi-2-naphthols in the presence of aluminum halides
Org. Biomol. Chem., 2019, V. 17, N 16, Pp 3971-3977 doi:10.1039/C9OB00640K, IF=3.49
- 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