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21
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Potapov K.V.
, Platonov D.N.
, Belyy A.Y.
, Novikov M.A.
, Tomilov Y.V.
, Anashkina A.A.
, Mukhina K.A.
, Kechko O.I.
, Solyev P.N.
, Novikov R.A.
, Makarov A.A.
, Mitkevich V.A.
Improved Synthesis of Effective 3-(Indolin-6-yl)-4-(N-pyrazole-sulfonamide)-1H-pyrrolo[2,3-b]pyridine-Based Inhibitors of NADPH Oxidase 2
International Journal of Molecular Sciences. 2025.
V.26. N8. 3647
. DOI: 10.3390/ijms26083647
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22
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Шулишов Е.В.
, Пантюх О.А.
, Стрельцова Е.Д.
, Менчиков Л.Г.
, Томилов Ю.В.
Каталитическое взаимодействие дициклопропилацетилена с диазометаном: синтез ивьяна[4]
Известия Академии наук. Серия химическая. 2025.
Т.74. №3. С.865-870.
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23
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Levina A.A.
, Borisov D.D.
, Novikov M.A.
, Shmelev M.A.
, Novikov R.A.
, Tomilov Y.V.
Reactions of β-styrylmalonates with aromatic aldehydes: the development of a catalytic version using gallium trichloride
Mendeleev Communications. 2025.
V.35. N3. P.261-263. DOI: 10.71267/mencom.7594
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24
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Ershova A.A.
, Ulchenko E.A.
, Borisov D.D.
, Budynina E.M.
, Novikov R.A.
, Tomilov Y.V.
1,3‐ and 1,2‐Zwitterionic Complexes of Donor‐Acceptor Cyclopropanes in Reactions with Arylallenes
Chemistry: A European Journal. 2025.
V.31. N51. e01226
. DOI: 10.1002/chem.202501226
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25
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Borisov D.D.
, Knyazev D.A.
, Novikov R.A.
, Tomilov Y.V.
Chemical transformations of 2-phenylcyclopropane-1,1-dinitrile under the action of Lewis acids
Mendeleev Communications. 2025.
V.35. N1. P.93-95. DOI: 10.71267/mencom.7574
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26
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Bobrova A.Y.
, Novikov M.A.
, Burykina J.V.
, Trainov K.P.
, Tomilov Y.V.
Fluorinated cyclopropanes for 2-heterosubstituted electron-rich indolizine synthesis
Organic & Biomolecular Chemistry. 2025.
V.23. P.6616-6624. DOI: 10.1039/d5ob00628g
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27
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Borisova I.A.
, Borisov D.D.
, Kolotyrkina N.G.
, Zhou B.
, Ye L.
, Novikov R.A.
, Tomilov Y.V.
GaCl3‐Promoted Reactions of Donor‐Acceptor Cyclopropanes with Conjugated Diacetylenes
Asian Journal of Organic Chemistry. 2025.
V.14. N9. P.e00392. DOI: 10.1002/ajoc.202500392
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28
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Borisov D.D.
, Platonov D.N.
, Sokolov N.A.
, Novikov R.A.
, Tomilov Y.V.
Formal High‐Order Cycloadditions of Donor‐Acceptor Cyclopropanes with Cycloheptatrienes
Angewandte Chemie International Edition. 2024.
V.63. N39. e202410081
. DOI: 10.1002/anie.202410081
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29
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Sergeev P.G.
, Novikov R.A.
, Tomilov Y.V.
Cyclization reactions of cyclopropane derivatives with conjugated carbo- and heterosystems
Russian Chemical Reviews. 2024.
Т.93. №3. RCR5111
. DOI: 10.59761/rcr5111
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30
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Novikov R.A.
, Borisov D.D.
, Denisov D.A.
, Novikov M.A.
, Potapov K.V.
, Tkachev Y.V.
, Tomilov Y.V.
The concept of Gallium-controlled double C–H functionalization of aliphatic CH2-groups driven by Vinyl carbocations
Nature Communications. 2024.
V.15. N1. 8073
. DOI: 10.1038/s41467-024-51237-5
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31
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Borisov D.D.
, Ershova A.A.
, Platonov D.N.
, Novikov R.A.
, Tomilov Y.V.
Pathways of reactions of 2-arylcyclopropane-1,1-dicarboxylates with monosubstituted cycloheptatrienes under the action of GaCl3
Russian Chemical Bulletin. 2024.
V.73. N5. P.1229-1236. DOI: 10.1007/s11172-024-4239-1
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32
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Egorov M.P.
, Ananikov V.P.
, Baskir E.G.
, Boganov S.E.
, Bogdan V.I.
, Vereshchagin A.N.
, Vil’ V.A.
, Dalinger I.L.
, Dilman A.D.
, Eliseev O.L.
, Zlotin S.G.
, Knyazeva E.A.
, Kogan V.M.
, Kononov L.O.
, Krayushkin M.M.
, Krylov V.B.
, Kustov L.M.
, Levin V.V.
, Lichitsky B.V.
, Medvedev M.G.
, Nifantiev N.E.
, Rakitin O.A.
, Sakharov A.M.
, Svitanko I.V.
, Smirnov G.A.
, Stakheev A.Y.
, Syroeshkin M.A.
, Terent’ev A.O.
, Tomilov Y.V.
, Tretyakov E.V.
, Trushkov I.V.
, Fershtat L.L.
, Chaliy V.A.
, Shirinian V.Z.
Current trends in organic chemistry: contribution of the N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences
Russian Chemical Bulletin. 2024.
V.73. N9. P.2423-2532. DOI: 10.1007/s11172-024-4366-8
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33
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Novikov R.A.
, Platonov D.N.
, Belyy A.Y.
, Potapov K.V.
, Novikov M.A.
, Tomilov Y.V.
, Kechko O.I.
, Seregina T.A.
, Solyev P.N.
, Mitkevich V.A.
Development of a New Inhibitor of Bacterial Cystathionine γ-Lyase Based on 6-Bromoindole and Aminothiophene
Molecular Biology. 2024.
V.58. N6. P.1082-1088. DOI: 10.1134/s0026893324700584
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34
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Sokolova A.D.
, Platonov D.N.
, Belyy A.Y.
, Salikov R.F.
, Erokhin K.S.
, Tomilov Y.V.
The Antiaromatic Nucleophilic Substitution Reaction (SNAAr) in Cycloheptatrienyl-Anion Containing Zwitterions with a Möbius-Aromatic Intermediate
Organic Letters. 2024.
V.26. N28. P.5877-5882. DOI: 10.1021/acs.orglett.4c01446
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35
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Novikov R.A.
, Borisov D.D.
, Tomilov Y.V.
Cycloaddition and Annulation Reactions of Donor–Acceptor Cyclopropanes
В сборнике
Donor Acceptor Cyclopropanes in Organic Synthesis.
– Wiley‐VCH GmbH.,
2024.
– C.37-138. – ISBN 9783527835652. DOI: 10.1002/9783527835652.ch3
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36
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Salikov R.F.
, Belyy A.Y.
, Ilyushchenko M.K.
, Platonov D.N.
, Sokolova A.D.
, Tomilov Y.V.
Antiaromaticity of Cycloheptatrienyl Anions: Structure, Acidity, and Magnetic Properties
Chemistry: A European Journal. 2024.
V.30. N41. e202401041
. DOI: 10.1002/chem.202401041
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37
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Borisov D.D.
, Novikov R.A.
, Tomilov Y.V.
Three-Component Synthesis of Substituted Perhydropyrans from β-Styrylmalonates, Aldehydes, and Alkoxyaluminum Dichlorides
Organic Letters. 2024.
V.26. N5. P.1022-1027. DOI: 10.1021/acs.orglett.3c04097
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38
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Belyy A.Y.
, Sokolova A.D.
, Salikov R.F.
, Platonov D.N.
, Tomilov Y.V.
Investigation of reactions of CH-acids with generated in situ N-[1,2-bis(methoxycarbonyl)vinyl]pyridinium in the synthesis of 1,2,3,4,5,6,7-hepta(methoxycarbonyl)cycloheptatriene
Russian Chemical Bulletin. 2024.
V.73. N5. P.1455-1459. DOI: 10.1007/s11172-024-4265-z
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39
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Novikov M.A.
, Potapov K.V.
, Novikov R.A.
, Solyev P.N.
, Tomilov Y.V.
, Kochetkov S.N.
, Makarov A.A.
, Mitkevich V.A.
A convenient synthesis of a chlorobenzothiophenyl-indole-based inhibitor of bacterial cystathionine γ-lyase
Mendeleev Communications. 2024.
V.34. N2. P.255-258. DOI: 10.1016/j.mencom.2024.02.030
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40
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Sokolova A.D.
, Belyy A.Y.
, Salikov R.F.
, Platonov D.N.
, Tomilov Y.V.
Cyсlopentadienone and Pyrone Derivatives as Precursors of Electron-Deficient Cycloheptatrienes. Quantum Chemical Investigation and Synthesis
Synthesis-Stuttgart. 2024.
V.56. N16. P.2581-2587. DOI: 10.1055/a-2317-6659
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