Unexpected cyclization ortho-nitrochalcones into 2-alkylideneindolin-3-ones

Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/12154

Title:	Unexpected cyclization ortho-nitrochalcones into 2-alkylideneindolin-3-ones
Authors:	Aksenov, N. A. Аксенов, Н. А. Aksenov, D. A. Аксенов, Д. А. Arutiunov, N. A. Арутюнов, Н. А. Aksenova, D. S. Аксенова, Д. С. Aksenov, A. V. Аксенов, А. В. Rubin, M. A. Рубин, М. А.
Keywords:	Addition reaction;Cascade cyclization;Chalcones;Cyanide anions;Michael additions;Cyclization
Issue Date:	2020
Publisher:	Royal Society of Chemistry
Citation:	Aksenov, 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 18440-18450
Series/Report no.:	RSC Advances
Abstract:	An 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 reaction
URI:	http://hdl.handle.net/20.500.12258/12154
Appears in Collections:	Статьи, проиндексированные в SCOPUS, WOS

Files in This Item:

File	Description	Size	Format
scopusresults 1314 .pdf Restricted Access		1.01 MB	Adobe PDF	View/Open
WoS 840 .pdf Restricted Access		188.5 kB	Adobe PDF	View/Open

Репозиторий научных и учебно-методических публикаций