Issue 20, 2015

Copper-catalyzed aerobic oxidative amination of C(sp3)–H bonds: synthesis of imidazo[1,5-a]pyridines

Abstract

Copper-catalyzed synthesis of imidazo[1,5-a]pyridine-1-carboxylates through oxidative amination of C(sp3)–H bonds under mild aerobic conditions with broad substrate scope is described. Use of naturally abundant air as the sole oxidant was found to be efficient and selective. The present protocol is also applicable for direct synthesis of functionalized imidazo[1,5-a]pyridines from amino acid derivatives.

Graphical abstract: Copper-catalyzed aerobic oxidative amination of C(sp3)–H bonds: synthesis of imidazo[1,5-a]pyridines

Supplementary files

Article information

Article type
Communication
Submitted
25 Feb 2015
Accepted
14 Apr 2015
First published
14 Apr 2015

Org. Biomol. Chem., 2015,13, 5602-5607

Author version available

Copper-catalyzed aerobic oxidative amination of C(sp3)–H bonds: synthesis of imidazo[1,5-a]pyridines

D. Chandra Mohan, S. Nageswara Rao, C. Ravi and S. Adimurthy, Org. Biomol. Chem., 2015, 13, 5602 DOI: 10.1039/C5OB00381D

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