Issue 2, 2016

I2-promoted aerobic oxidative coupling of acetophenes with amines under metal-free conditions: facile access to α-ketoamides

Abstract

A novel and efficient I2-promoted oxidative coupling of acetophenes with amines to α-ketoamides is presented, which employs O2 as an environmentally friendly oxidant under metal-free conditions. Based on a series of control experiments and radical trapping experiments, plausible reaction mechanism was proposed and iminium ion was identified as a significant intermediate in this process. This methodology is a feasible, mild approach to α-ketoamides in good yields.

Graphical abstract: I2-promoted aerobic oxidative coupling of acetophenes with amines under metal-free conditions: facile access to α-ketoamides

Supplementary files

Article information

Article type
Paper
Submitted
14 Nov 2015
Accepted
12 Dec 2015
First published
15 Dec 2015

RSC Adv., 2016,6, 1503-1507

I2-promoted aerobic oxidative coupling of acetophenes with amines under metal-free conditions: facile access to α-ketoamides

S. Guo, Z. Fang, Z. Yang, C. Liu, Z. Dai, L. Zhao and K. Guo, RSC Adv., 2016, 6, 1503 DOI: 10.1039/C5RA24062J

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