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Articles (107)

# Публикация
1 Zayakin I. , Tretyakov E. , Akyeva A. , Syroeshkin M. , Burykina J. , Dmitrenok A. , Korlyukov A. , Nasyrova D. , Bagryanskaya I. , Stass D. , Ananikov V.
Overclocking Nitronyl Nitroxide Gold Derivatives in Cross‐Coupling Reactions
Chemistry - A European Journal. 2023. V.29. N6. e202203118 . DOI: 10.1002/chem.202203118 WOS РИНЦ OpenAlex
2 Asanbaeva N.B. , Gurskaya L.Y. , Polienko Y.F. , Rybalova T.V. , Kazantsev M.S. , Dmitriev A.A. , Gritsan N.P. , Haro-Mares N. , Gutmann T. , Buntkowsky G. , Tretyakov E.V. , Bagryanskaya E.G.
Effects of Spiro-Cyclohexane Substitution of Nitroxyl Biradicals on Dynamic Nuclear Polarization
Molecules. 2022. V.27. N10. P.3252. DOI: 10.3390/molecules27103252 WOS Scopus РИНЦ OpenAlex
3 Tretyakov E.V. , Petunin P.V. , Zhivetyeva S.I. , Gorbunov D.E. , Gritsan N.P. , Fedin M.V. , Stass D.V. , Samoilova R.I. , Bagryanskaya I.Y. , Shundrina I.K. , Bogomyakov A.S. , Kazantsev M.S. , Postnikov P.S. , Trusova M.E. , Ovcharenko V.I.
Platform for High-Spin Molecules: A Verdazyl-Nitronyl Nitroxide Triradical with Quartet Ground State
Journal of the American Chemical Society. 2021. V.143. N21. P.8164–8176. DOI: 10.1021/jacs.1c02938 WOS Scopus РИНЦ OpenAlex
4 Politanskaya L. , Tretyakov E. , Xi C.
Synthesis of polyfluorinated 4-hydroxyquinolin-2(1H)-ones based on the cyclization of 2-alkynylanilines with carbon dioxide
Journal of Fluorine Chemistry. 2021. V.242. 109720 . DOI: 10.1016/j.jfluchem.2020.109720 WOS Scopus РИНЦ OpenAlex
5 Tretyakov E.V. , Maksimov A.M. , Nikul’shin P.V. , Mezhenkova T.V.
An efficient approach to the synthesis of 2,3,4,5-tetrafluorophenol
Russian Chemical Bulletin. 2021. V.70. N5. P.995-998. DOI: 10.1007/s11172-021-3178-3 WOS Scopus РИНЦ OpenAlex
6 Третьяков Е.В. , Максимов А.М. , Никульшин П.В. , Меженкова Т.В.
Эффективный подход к синтезу 2,3,4,5-тетрафторфенола
Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2021. Т.70. №5. С.995-998. РИНЦ
7 Tretyakov E.V. , Lomanovich K.A. , Bagryanskaya E.G. , Romanenko G.V. , Bogomyakov A.S. , Zueva E.M. , Petrova M.M. , Dmitriev A.A. , Gritsan N.P.
2-(8-Iodonaphthalen-1-yl)-Substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
European Journal of Organic Chemistry. 2021. V.2021. N17. P.2355-2361. DOI: 10.1002/ejoc.202100138 WOS Scopus РИНЦ OpenAlex
8 Selivanova G.A. , Tretyakov E.V.
Fluorinated benzimidazoles for medicinal chemistry and new materials
Russian Chemical Bulletin. 2020. V.69. N5. P.838-858. DOI: 10.1007/s11172-020-2842-3 WOS Scopus РИНЦ OpenAlex
9 Tretyakov E. , Tkacheva A. , Romanenko G. , Bogomyakov A. , Stass D. , Maryasov A. , Zueva E. , Trofimov B. , Ovcharenko V.
(Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
Molecules. 2020. V.25. N7. 1503 . DOI: 10.3390/molecules25071503 WOS Scopus РИНЦ OpenAlex
10 Votkina D.E. , Petunin P.V. , Zhivetyeva S.I. , Bagryanskaya I.Y. , Uvarov M.N. , Kazantsev M.S. , Trusova M.E. , Tretyakov E.V. , Postnikov P.S.
Preparation of Multi-Spin Systems: A Case Study of Tolane-Bridged Verdazyl-Based Hetero-Diradicals
European Journal of Organic Chemistry. 2020. V.2020. N13. P.1996-2004. DOI: 10.1002/ejoc.202000044 WOS Scopus РИНЦ OpenAlex
11 Селиванова Г.А. , Третьяков Е.В.
ФТОРИРОВАННЫЕ БЕНЗИМИДАЗОЛЫ ДЛЯ МЕДИЦИНСКОЙ ХИМИИ И НОВЫХ МАТЕРИАЛОВ
Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2020. №5. С.838-858. РИНЦ
12 Ten Y.A. , Troshkova N.M. , Tretyakov E.V.
From spin-labelled fused polyaromatic compounds to magnetically active graphene nanostructures
Russian Chemical Reviews. 2020. V.89. N7. P.693-712. DOI: 10.1070/RCR4923 WOS Scopus РИНЦ OpenAlex
13 Ten Y.A. , Troshkova N.M. , Tretyakov E.V.
Method of preparation of alkylated 1,3-diphenylpropan-2-ones, the components for assembly of graphene nanostructures
Russian Chemical Bulletin. 2020. V.69. N1. P.172-175. DOI: 10.1007/s11172-020-2740-8 WOS Scopus РИНЦ OpenAlex
14 Gurskaya L. , Rybalova T. , Beregovaya I. , Zaytseva E. , Kazantsev M. , Tretyakov E.
Aromatic nucleophilic substitution: A case study of the interaction of a lithiated nitronyl nitroxide with polyfluorinated quinoline-N-oxides
Journal of Fluorine Chemistry. 2020. V.237. 109613 . DOI: 10.1016/j.jfluchem.2020.109613 WOS Scopus РИНЦ OpenAlex
15 Romanov V. , Tretyakov E. , Selivanova G. , Li J.L. , Bagryanskaya I. , Makarov A. , Luneau D.
Synthesis and structure of fluorinated (Benzo[d]imidazol-2-yl)methanols: Bench compounds for diverse applications
Crystals. 2020. V.10. N9. 786 :1-16. DOI: 10.3390/cryst10090786 WOS Scopus РИНЦ OpenAlex
16 Zayakin I. , Bagryanskaya I. , Stass D. , Kazantsev M. , Tretyakov E.
Synthesis and structure of (Nitronyl nitroxide-2-ido)(tert-butyldiphenylphosphine)gold(i) and-(di(tert-butyl)phenylphosphine)gold(i) derivatives; their comparative study in the cross-coupling reaction
Crystals. 2020. V.10. N9. 770 :1-12. DOI: 10.3390/cryst10090770 WOS Scopus РИНЦ OpenAlex
17 Politanskaya L. , Bagryanskaya I. , Tretyakov E. , Xi C.
Highly efficient synthesis of novel fluorinated 3-amino-2-mercaptobenzothiazole-2(3H)-thione derivatives
Journal of Fluorine Chemistry. 2020. V.239. 109628 . DOI: 10.1016/j.jfluchem.2020.109628 WOS Scopus РИНЦ OpenAlex
18 Gromova M.A. , Kharitonov Y.V. , Politanskaya L.,.V. , Tretyakov E.,.V. , Shults E.E.
A facile approach to hybrid compounds containing a tricyclic diterpenoid and fluorine-substituted heterocycles
Journal of Fluorine Chemistry. 2020. V.236. 109554 . DOI: 10.1016/j.jfluchem.2020.109554 WOS Scopus РИНЦ OpenAlex
19 Politanskaya L. , Tretyakov E.
Directed synthesis of fluorine containing 2,3-dihydrobenzo[b][1,4]oxathiine derivatives from polyfluoroarenes
Journal of Fluorine Chemistry. 2020. V.236. 109592 . DOI: 10.1016/j.jfluchem.2020.109592 WOS Scopus РИНЦ OpenAlex
20 Fedyushin P. , Rybalova T. , Asanbaeva N. , Bagryanskaya E. , Dmitriev A. , Gritsan N. , Kazantsev M. , Tretyakov E.
Synthesis of Nitroxide Diradical Using a New Approach
Molecules. 2020. V.25. N11. 2701 . DOI: 10.3390/molecules25112701 WOS Scopus РИНЦ OpenAlex

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