Pd-Catalyzed Direct ortho-C-H Arylation of Aromatic Ketones Enabled by a Transient Directing Group

Org Lett. 2017 Apr 7;19(7):1562-1565. doi: 10.1021/acs.orglett.7b00363. Epub 2017 Mar 24.

Abstract

The Pd-catalyzed direct C(sp2)-H arylation of aromatic ketones using a transient directing group is described. The ketimine/carboxylate bidentate directing group in situ generated from aromatic ketone and glycine enabled a palladium-catalyzed ortho-C-H arylation, which shows extensive substrate compatibility.

Publication types

  • Research Support, Non-U.S. Gov't