Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/123456789/31112
Title: Synthesis of Dimethyl (Z)-((3-oxoindolin-2-ylidene) (aryl)methyl)phosphonates Through Tandem Cadogan and Arbuzov Reactions
Authors: Aksenov, N. A.
Аксенов, Н. А.
Aksenov, D. A.
Аксенов, Д. А.
Ganusenko, D. D.
Ганусенко, Д. Д.
Kurlikov, A. E.
Курликов, А. Э.
Barbolin, A. P.
Барболин, А. П.
Karaseva, P. S.
Карасева, П. С.
Aksenov, A. V.
Аксенов, А. В.
Keywords: Arbuzov reaction;Phosphonates;Cadogan–Sundberg reaction;Indoles;Chalcones;Phosphites;Reduction
Issue Date: 2025
Publisher: Multidisciplinary Digital Publishing Institute (MDPI)
Citation: Aksenov N.A., Aksenov D.A., Ganusenko D.D., Kurlikov A.E., Barbolin A.P., Karaseva P.S., Aksenov A.V. Synthesis of Dimethyl (Z)-((3-oxoindolin-2-ylidene) (aryl)methyl)phosphonates Through Tandem Cadogan and Arbuzov Reactions // MolBank. - 2025. - 2025 (2). - art. no. M2002. - DOI: 10.3390/M2002
Series/Report no.: MolBank
Abstract: A novel method employing a tandem Cadogan and Arbuzov reaction sequence has been developed, providing access to a series of previously unreported dimethyl (Z)-((3-oxoindolin-2-ylidene)(aryl)methyl)phosphonates. Restricted rotation of the aryl substituent, particularly in the presence of ortho substituents, gives axial chirality to these compounds.
URI: https://dspace.ncfu.ru/handle/123456789/31112
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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