Issue 6, 2017

Nickel-catalyzed product-controllable amidation and imidation of sp3 C–H bonds in substituted toluenes with sulfonamides

Abstract

A nickel-catalyzed product-controllable imidation and amidation of sp3 C–H bonds in substituted toluenes with sulfonamides were developed. Based on the change of the reaction time and atmosphere from N2 to O2, this reaction proceeded in high yields and excellent selectivity under different conditions. Mechanistic details were also described.

Graphical abstract: Nickel-catalyzed product-controllable amidation and imidation of sp3 C–H bonds in substituted toluenes with sulfonamides

Supplementary files

Article information

Article type
Communication
Submitted
05 Jan 2017
Accepted
11 Jan 2017
First published
17 Jan 2017

Org. Biomol. Chem., 2017,15, 1317-1320

Nickel-catalyzed product-controllable amidation and imidation of sp3 C–H bonds in substituted toluenes with sulfonamides

Z. Li, L. Jin and C. Cai, Org. Biomol. Chem., 2017, 15, 1317 DOI: 10.1039/C7OB00022G

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