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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/123456789/31112
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dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorGanusenko, D. D.-
dc.contributor.authorГанусенко, Д. Д.-
dc.contributor.authorKurlikov, A. E.-
dc.contributor.authorКурликов, А. Э.-
dc.contributor.authorBarbolin, A. P.-
dc.contributor.authorБарболин, А. П.-
dc.contributor.authorKaraseva, P. S.-
dc.contributor.authorКарасева, П. С.-
dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.date.accessioned2025-07-11T07:33:36Z-
dc.date.available2025-07-11T07:33:36Z-
dc.date.issued2025-
dc.identifier.citationAksenov 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/M2002ru
dc.identifier.urihttps://dspace.ncfu.ru/handle/123456789/31112-
dc.description.abstractA 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.ru
dc.language.isoenru
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)ru
dc.relation.ispartofseriesMolBank-
dc.subjectArbuzov reactionru
dc.subjectPhosphonatesru
dc.subjectCadogan–Sundberg reactionru
dc.subjectIndolesru
dc.subjectChalconesru
dc.subjectPhosphitesru
dc.subjectReductionru
dc.titleSynthesis of Dimethyl (Z)-((3-oxoindolin-2-ylidene) (aryl)methyl)phosphonates Through Tandem Cadogan and Arbuzov Reactionsru
dc.typeСтатьяru
vkr.instХимический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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