Tandem acceptorless dehydrogenative coupling-decyanation under nickel catalysis

TitleTandem acceptorless dehydrogenative coupling-decyanation under nickel catalysis
Publication TypeJournal Article
Year of Publication2021
AuthorsMidya, SP, Subaramanian, M, Babu, R, Yadav, V, Balaraman, E
JournalJournal of Organic Chemistry
Volume86
Issue11
Pagination7552-7562
Date PublishedJUN
Type of ArticleArticle
ISSN0022-3263
AbstractThe development of new catalytic processes based on abundantly available starting materials by cheap metals is always a fascinating task and marks an important transition in the chemical industry. Herein, a nickel-catalyzed acceptorless dehydrogenative coupling of alcohols with nitriles followed by decyanation of nitriles to access diversely substituted olefins is reported. This unprecedented C=C bond-forming methodology takes place in a tandem manner with the formation of formamide as a sole byproduct. The significant advantages of this strategy are the low-cost nickel catalyst, good functional group compatibility (ether, thioether, halo, cyano, ester, amino, N/O/S heterocycles; 43 examples), synthetic convenience, and high reaction selectivity and efficiency.
DOI10.1021/acs.joc.1c00592
Type of Journal (Indian or Foreign)Foreign
Impact Factor (IF)4.354
Divison category: 
Organic Chemistry

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