Issue 51, 2017

Palladium-catalyzed intermolecular carbonylative cross-coupling of heteroaryl C(sp2)–H bonds with amines: an efficient strategy for oxidative aminocarbonylation of azoles

Abstract

An efficient palladium-catalyzed oxidative aminocarbonylation of azoles has been developed. This system allows for intermolecular carbonylative cross-coupling of aromatic C(sp2)–H bonds with simple amines, which has often been asked for, but has not been realized so far. It provides a straightforward approach to a variety of azol-2-amides.

Graphical abstract: Palladium-catalyzed intermolecular carbonylative cross-coupling of heteroaryl C(sp2)–H bonds with amines: an efficient strategy for oxidative aminocarbonylation of azoles

Supplementary files

Article information

Article type
Communication
Submitted
27 Apr 2017
Accepted
07 Jun 2017
First published
07 Jun 2017

Chem. Commun., 2017,53, 6914-6917

Palladium-catalyzed intermolecular carbonylative cross-coupling of heteroaryl C(sp2)–H bonds with amines: an efficient strategy for oxidative aminocarbonylation of azoles

Q. Xing, H. Lv, C. Xia and F. Li, Chem. Commun., 2017, 53, 6914 DOI: 10.1039/C7CC03274A

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