Issue 31, 2018

Metal-free synthesis of imidazo[1,5-a]pyridines via elemental sulfur mediated sequential dual oxidative Csp3–H amination

Abstract

A simple and efficient approach has been developed for the synthesis of imidazo[1,5-a]pyridines using the elemental sulfur mediated sequential dual oxidative Csp3–H amination of 2-pyridyl acetates and amines under metal- and peroxide-free conditions. Broad substrate scope, operational simplicity and gram-scale ability make this chemistry very practical.

Graphical abstract: Metal-free synthesis of imidazo[1,5-a]pyridines via elemental sulfur mediated sequential dual oxidative Csp3–H amination

Supplementary files

Article information

Article type
Communication
Submitted
12 Jun 2018
Accepted
16 Jul 2018
First published
23 Jul 2018

Org. Biomol. Chem., 2018,16, 5570-5574

Metal-free synthesis of imidazo[1,5-a]pyridines via elemental sulfur mediated sequential dual oxidative Csp3–H amination

J. Sheng, J. Liu, H. Zhao, L. Zheng and X. Wei, Org. Biomol. Chem., 2018, 16, 5570 DOI: 10.1039/C8OB01391H

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