Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН
- A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
- E.Yu. Schmidt, B.A. Trofimov, I.A. Bidusenko, N.A. Cherimichkina, I.A. Ushakov, N.I. Protzuk, Yu.V. Gatilov
Base-Catalyzed Domino Cyclization of Acetylenes with Ketones to Functionalized Cyclopentenes
Org. Lett., 2014, 16 (15), pp 4040-4043. doi:10.1021/ol501881e, IF=6.323
- E.O. Shestakova, S.G. Il'yasov, I.A. Shchurova, V.S. Glukhacheva, D.S. Il'yasov, E.E. Zhukov, A.O. Bryzgalov, T.G. Tolstikova, Yu.V. Gatilov
Investigation of 1,4-Substituted 1,2,3-Triazole Derivatives as Antiarrhythmics: Synthesis, Structure, and Properties
Pharmaceuticals 2022, 15(12), 1443 doi:10.3390/ph15121443, IF=5.215
- I.B. Ivshina, N.A. Luchnikova, P.Yu. Maltseva, I.V. Ilyina, K.P. Volcho, Yu.V. Gatilov, D.V. Korchagina, N.A. Kostrikina, V.V. Sorokin, A.L. Mulyukin, N.F. Salakhutdinov
Biotransformation of (-)-Isopulegol by Rhodococcus rhodochrous
Pharmaceuticals 2022, 15(8), 964; doi:10.3390/ph15080964, IF=5.215
- M.B. Bushuev, V.A. Daletsky, D.P. Pishchur, Yu.V. Gatilov, I.V. Korolkov, E.B. Nikolaenkova, V.P. Krivopalov
Unprecedented bistability domain and interplay between spin crossover and polymorphism in a mononuclear iron(II) complex
Dalton Trans., 2014,43(10), 3906-3910. doi:10.1039/C3DT53440E, IF=4.97
- I. Philippov, Yu. Gatilov, A. Sonina, A. Vorob’ev
Oxidative [3+2]Cycloaddition of Alkynylphosphonates with Heterocyclic N-Imines: Synthesis of Pyrazolo[1,5-a]Pyridine-3-phosphonates
Molecules 2022, 27(22), 7913 doi:10.3390/molecules27227913, IF=4.927
- S.A. Dobrynin, M.M. Gulman, D.A. Morozov, I.F. Zhurko, A.I. Taratayko, Yu.S. Sotnikova, Yu.I. Glazachev, Yu.V. Gatilov, I.A. Kirilyuk
Synthesis of Sterically Shielded Nitroxides Using the Reaction of Nitrones with Alkynylmagnesium Bromides
Molecules 2022, 27(21), 7626 doi:10.3390/molecules27217626, IF=4.927
- V.V. Oreshko, K.S. Kovaleva, E.D. Mordvinova, O.I. Yarovaya, Yu.V. Gatilov, D.N. Shcherbakov, N.I. Bormotov, O.A. Serova, L.N. Shishkina, N.F. Salakhutdinov
Synthesis and Antiviral Properties of Camphor-Derived Iminothiazolidine-4-Ones and 2,3-Dihydrothiazoles
Molecules 2022, 27(15), 4761 doi:10.3390/molecules27154761, IF=4.927
- A.A. Munkuev, N.S. Dyrkheeva, T.E. Kornienko, E.S. Ilina, D.I. Ivankin, E.V. Suslov, D.V. Korchagina, Yu.V. Gatilov, A.L. Zakharenko, A.A. Malakhova, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
Adamantane-Monoterpenoid Conjugates Linked via Heterocyclic Linkers Enhance the Cytotoxic Effect of Topotecan
Molecules 2022, 27(11), 3374 doi:10.3390/molecules27113374, IF=4.927
- E. Benassi, T. Vaganova, E. Malykhin, Yu. Gatilov, L. Nurtay, H. Fanc
Intermolecular Interactions in the Crystalline Structure of Some Polyhalogenated Di– and Triamino Pyridines: Spectroscopical Perspectives
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, V. 281, 15 November 2022, 121632 doi:10.1016/j.saa.2022.121632, IF=4.83
- 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
- S.F. Vasilevsky, D.S. Baranov, V.I. Mamatyuk, D.S. Fadeev, Yu.V. Gatilov, A.A. Stepanov, N.V. Vasilieva, I.V. Alabugin
Conformational Flexibility of Fused Tetracenedione Propellers Obtained from One-Pot Reductive Dimerization of Acetylenic Quinones
J. Org. Chem., 2015, 80 (3), pp 1618-1631 doi:10.1021/jo502543b, IF=4.721
- A.Yu. Makarov, F. Blockhuys, I.Yu. Bagryanskaya, Yu.V. Gatilov, M.M. Shakirov, A.V. Zibarev
Experimental and Computational Study on the Structure and Properties of Herz Cations and Radicals: 1,2,3-Benzodithiazolium, 1,2,3-Benzodithiazolyl, and Their Se Congeners
Inorganic Chemistry, 2013, V. 52, N 7, P. 3699-3710. doi:10.1021/ic302203t, IF=4.592
- I.A. Kirilyuk, Yu.F. Polienko, O.A. Krumkacheva, R.K. Strizhakov, Yu.V. Gatilov, I.A. Grigor’ev, E.G. Bagryanskaya
Synthesis of 2,5-Bis(spirocyclohexane)-Substituted Nitroxides of Pyrroline and Pyrrolidine Series, Including Thiol-Specific Spin Label: An Analogue of MTSSL with Long Relaxation Time
J. Org. Chem., 2012, V. 77, N 18, 8016–8027. doi:10.1021/jo301235j, IF=4.449
- V.N. Kovtonyuk, Yu.V. Gatilov, P.V. Nikul’shin, R.A. Bredikhin
Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene
Molecules 2021, 26(3), 526 doi:10.3390/molecules26030526, IF=4.411
- A.S. Volobueva, O.I. Yarovaya, M.V. Kireeva, S.S. Borisevich, K.S. Kovaleva, I.Ya. Mainagashev, Yu.V. Gatilov, M.G. Ilyina, V.V. Zarubaev, N.F. Salakhutdinov
Discovery of New Ginsenol-like Compounds with High Antiviral Activity
Molecules, 2021, 26(22), 6794 doi:10.3390/molecules26226794, IF=4.41
- S.A. Dobrynin, M.S. Usatov, I.F. Zhurko, D.A. Morozov, Yu.F. Polienko, Yu.I. Glazachev, D.A. Parkhomenko, M.A. Tyumentsev, Yu.V. Gatilov, E.I. Chernyak, E.G. Bagryanskaya, I.A. Kirilyuk
A Simple Method of Synthesis of 3-Carboxy-2,2,5,5-Tetraethylpyrrolidine-1-oxyl and Preparation of Reduction-Resistant Spin Labels and Probes of Pyrrolidine Series
Molecules 2021, 26(19), 5761 doi:10.3390/molecules26195761, IF=4.41
- D.S. Baranov, A.A. Popov, D.A. Nevostruev, A.A. Dmitriev, Yu.V. Gatilov, E.S. Kobeleva
One-Pot Synthesis of 2-R-Naphtho[2,3-b]thiophene-4,9-diones via Cyclization of 2-(R-Ethynyl)-1,4-naphthoquinones with Na2S2O3
The Journal of Organic Chemistry, 2021, V. 86, N. 17, Pp. 11361-11369 doi:10.1021/acs.joc.1c00852, IF=4.354
- A.Yu. Makarov, V.V. Zhivonitko, A.G. Makarov, S.B. Zikirin, I.Yu. Bagryanskaya, V.A. Bagryansky, Yu.V. Gatilov, I.G. Irtegova, M.M. Shakirov, A.V. Zibarev
Interaction of 1,3,2,4-Benzodithiadiazines and Their 1-Se Congeners with Ph3P and Some Properties of the Iminophosphorane Products
Inorg. Chem., 2011, V. 50, 3017–3027. doi:10.1021/ic102565x, IF=4.324
- M.B. Bushuev, D.P. Pishchur, V.A. Logvinenko, Yu.V. Gatilov, I.V. Korolkov, I.K. Shundrina, E.B. Nikolaenkova, V.P. Krivopalov
A mononuclear iron(II) complex: cooperativity, kinetics and activation energy of the solvent-dependent spin transition
Dalton Trans., 2016,45(1), 107-120 doi:10.1039/C5DT03750F, IF=4.177