Nickel-catalyzed direct alkynylation of C(sp2)-H bonds of amides: an “inverse sonogashira strategy” to ortho-alkynylbenzoic acids. just accepted
Title | Nickel-catalyzed direct alkynylation of C(sp2)-H bonds of amides: an “inverse sonogashira strategy” to ortho-alkynylbenzoic acids. just accepted |
Publication Type | Journal Article |
Year of Publication | 2016 |
Authors | Landge, VGokulkrish, Shewale, CH, Jaiswal, G, Sahoo, MKumar, Midya, SPrasad, Balaraman, E |
Journal | Catalysis Science & Technology |
Volume | 6 |
Issue | 6 |
Pagination | 1946-1951 |
Date Published | OCT |
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. |
DOI | 10.1039/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