Issue 17, 2018

Metal-free oxidative coupling of quinoxalin-2(1H)-ones with arylaldehydes leading to 3-acylated quinoxalin-2(1H)-ones

Abstract

A facile TBHP-mediated direct oxidative coupling of quinoxalin-2(1H)-ones with arylaldehydes has been developed under metal-free conditions. This method provided a convenient and efficient approach to various 3-acylated quinoxalin-2(1H)-ones from readily available starting materials with excellent regioselectivity. This reaction proceeded efficiently under mild conditions over a broad range of substrates and with functional group tolerance.

Graphical abstract: Metal-free oxidative coupling of quinoxalin-2(1H)-ones with arylaldehydes leading to 3-acylated quinoxalin-2(1H)-ones

Supplementary files

Article information

Article type
Paper
Submitted
25 Jan 2018
Accepted
05 Apr 2018
First published
10 Apr 2018

Org. Biomol. Chem., 2018,16, 3203-3212

Metal-free oxidative coupling of quinoxalin-2(1H)-ones with arylaldehydes leading to 3-acylated quinoxalin-2(1H)-ones

J. Yuan, J. Fu, S. Liu, Y. Xiao, P. Mao and L. Qu, Org. Biomol. Chem., 2018, 16, 3203 DOI: 10.1039/C8OB00206A

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