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Dive into the research topics where Александр Сергеевич Филатов is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Projects
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RFBR_mol_a_2018 - 2: Реакции циклопропенов с азометинилидами как эффективный подход к стереоселективному синтезу азотсодержащих полициклических гетероциклов: 2019 г. этап 2
Борисов, Е. В., Демкив, В. О. & Филатов, А. С.
3/08/19 → 10/03/20
Project
Research output
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Construction of Spiro[3-azabicyclo[3.1.0]hexanes] via 1,3-Dipolar Cycloaddition of 1,2-Diphenylcyclopropenes to Ninhydrin-Derived Azomethine Ylides
Ван, С., Филатов, А. С., Lozovskiy, S. V., Shmakov, S. V., Хорошилова, О. В., Ларина, А. Г., Селиванов, С. И., Бойцов, В. М. & Степаков, А. В., 18 Jan 2021, (E-pub ahead of print) In: Synthesis (Germany).Research output › peer-review
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Concise Synthesis of Tryptanthrin Spiro Analogues with In Vitro Antitumor Activity Based on One-Pot, Three-Component 1, 3-Dipolar Cycloaddition of Azomethine Ylides to Сyclopropenes
Filatov, A. S., Knyazev, N. A., Shmakov, S. V., Bogdanov, A. A., Ryazantsev, M. N., Shtyrov, A. A., Starova, G. L., Molchanov, A. P., Larina, A. G., Boitsov, V. M. & Stepakov, A. V., 2019, In: Synthesis. 51, 3, p. 713-729 17 p.Research output › peer-review
8 Citations (Scopus) -
Stereo- and Regioselective 1,3-Dipolar Cycloaddition of the Stable Ninhydrin-Derived Azomethine Ylide to Cyclopropenes: Trapping of Unstable Cyclopropene Dipolarophiles
Filatov, A. S., Wang, S., Khoroshilova, O. V., Lozovskiy, S. V., Larina, A. G., Boitsov, V. M. & Stepakov, A. V., 7 Jun 2019, In: The Journal of organic chemistry. 84, 11, p. 7017-7036 20 p.Research output › peer-review
12 Citations (Scopus) -
A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones.
Филатов, А. С., Князев, Н. А., Рязанцев, М. Н., Суслонов, В. В., Ларина, А. Г., Молчанов, А. П., Костиков, Р. Р., Бойцов, В. М. & Степаков, А. В., 21 Feb 2018, In: Organic Chemistry Frontiers. 5, 4, p. 595-605 11 p.Research output › peer-review
23 Citations (Scopus) -
Synthesis of isoxazolopyrrolo[2,1-a]isoquinoline, isoxazolo[5',4': 1,2]indolizino[8,7-b]indole, and isoxazolo- [5,4-a]thieno[2,3-g]indolizine derivatives by intramolecular cyclization of hydroxylactams constituting a fragment of the pyrroloisoxazole system
Lenshmidt, L. V., Ledovskaya, M. S., Larina, A. G., Filatov, A. S., Molchanov, A. P., Kostikov, R. R. & Stepakov, A. V., 2018, In: Russian Journal of Organic Chemistry. 54, 1, p. 112-125 14 p.Research output › peer-review
3 Citations (Scopus)