Issue 24, 2015

Nickel-catalyzed synthesis of diarylsulfides and sulfones via C–H bond functionalization of arylamides

Abstract

The direct sulfenylation and sulfonylation of (sp2)C–H bonds of benzamide derivatives were achieved using a Ni catalyst with the aid of an 8-aminoquinoline moiety as a bidentate directing group. These protocols represent a convenient route for the formation of valuable diaryl sulfides and sulfones in moderate to excellent yields.

Graphical abstract: Nickel-catalyzed synthesis of diarylsulfides and sulfones via C–H bond functionalization of arylamides

Supplementary files

Article information

Article type
Paper
Submitted
26 Jan 2015
Accepted
13 May 2015
First published
13 May 2015

Org. Biomol. Chem., 2015,13, 6803-6813

Author version available

Nickel-catalyzed synthesis of diarylsulfides and sulfones via C–H bond functionalization of arylamides

V. P. Reddy, R. Qiu, T. Iwasaki and N. Kambe, Org. Biomol. Chem., 2015, 13, 6803 DOI: 10.1039/C5OB00149H

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