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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/12154
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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.authorArutiunov, N. A.-
dc.contributor.authorАрутюнов, Н. А.-
dc.contributor.authorAksenova, D. S.-
dc.contributor.authorАксенова, Д. С.-
dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2020-06-30T10:10:02Z-
dc.date.available2020-06-30T10:10:02Z-
dc.date.issued2020-
dc.identifier.citationAksenov, N.A., Aksenov, D.A., Arutiunov, N.A., Aksenova, D.S., Aksenov, A.V., Rubin, M. Unexpected cyclization ortho-nitrochalcones into 2-alkylideneindolin-3-ones // RSC Advances. - 2020. - Volume 10. - Issue 31. -Pages 18440-18450ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/12154-
dc.description.abstractAn original, facile, and highly efficient method for the preparation of 2-(3-oxoindolin-2-ylidene)acetonitriles fromortho-nitrochalcones is described. The featured transformation is a triggered Michael addition of the cyanide anion to the chalcone followed by a cascade cyclization mechanistically related to the Baeyer-Drewson reactionru
dc.language.isoenru
dc.publisherRoyal Society of Chemistryru
dc.relation.ispartofseriesRSC Advances-
dc.subjectAddition reactionru
dc.subjectCascade cyclizationru
dc.subjectChalconesru
dc.subjectCyanide anionsru
dc.subjectMichael additionsru
dc.subjectCyclizationru
dc.titleUnexpected cyclization ortho-nitrochalcones into 2-alkylideneindolin-3-onesru
dc.typeСтатьяru
vkr.instИнститут математики и естественных наукru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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