Nickel-catalyzed direct alkynylation of C(sp2)-H bonds of amides: an “inverse sonogashira strategy” to ortho-alkynylbenzoic acids. just accepted

TitleNickel-catalyzed direct alkynylation of C(sp2)-H bonds of amides: an “inverse sonogashira strategy” to ortho-alkynylbenzoic acids. just accepted
Publication TypeJournal Article
Year of Publication2016
AuthorsLandge, VGokulkrish, Shewale, CH, Jaiswal, G, Sahoo, MKumar, Midya, SPrasad, Balaraman, E
JournalCatalysis Science & Technology
Volume6
Issue6
Pagination1946-1951
Date PublishedOCT
Abstract

Nickel-catalyzed direct alkynylation of C(sp2)–H bonds of amides using commercially available, inexpensive 8-aminoquinoline as a removable bidentate directing group is described. The present ortho-alkynylation has a broad substrate scope, functional group tolerance and high regiocontrol, and can be scaled up. The efficiency and selectivity of this strategy provide sustainable routes to a diverse array of ortho-alkynylbenzoic acids under Ni(II)-catalyzed conditions.

DOI10.1039/C5CY01299F
Funding Agency

Council of Scientific & Industrial Research (CSIR) - India

Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)5.287
Divison category: 
Catalysis and Inorganic Chemistry