Issue 7, 2016

Nickel(ii)-catalyzed direct arylation of aryl C–H bonds with aryl-boron reagents directed by a removable bidentate auxiliary

Abstract

Ni(II)-catalyzed C–H arylation using Ar2I+X or ArX as the arylating reagent via oxidative addition has been well investigated. However, the analogous cross-coupling of C–H bonds with organoboron reagents via transmetallation remains a great challenge. Here we report the first Ni(II)-catalyzed direct C–H arylation with arylboronic acid esters assisted by a removable bidentate auxiliary. This procedure is scalable and compatible with a wide range of functional groups, providing a complementary protocol for the synthesis of biaryl compounds.

Graphical abstract: Nickel(ii)-catalyzed direct arylation of aryl C–H bonds with aryl-boron reagents directed by a removable bidentate auxiliary

Supplementary files

Article information

Article type
Research Article
Submitted
09 Apr 2016
Accepted
20 May 2016
First published
23 May 2016

Org. Chem. Front., 2016,3, 897-900

Nickel(II)-catalyzed direct arylation of aryl C–H bonds with aryl-boron reagents directed by a removable bidentate auxiliary

B. Liu, Z. Zhang, X. Li and B. Shi, Org. Chem. Front., 2016, 3, 897 DOI: 10.1039/C6QO00149A

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