Issue 5, 2019

Chan–Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical N-arylsulfamides

Abstract

An efficient method was developed for the synthesis of unsymmetrical N-arylsulfamides using sulfamoyl azides and arylboronic acids in the presence of 10 mol% of copper chloride as the catalyst. The reaction was facilitated in MeOH in an open flask at room temperature. Unlike the coupling of sulfamides and boronic acids, the use of sulfamoyl azides was found to be beneficial with respect to the yield and reaction time.

Graphical abstract: Chan–Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical N-arylsulfamides

Supplementary files

Article information

Article type
Paper
Submitted
07 Nov 2018
Accepted
14 Jan 2019
First published
18 Jan 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 2493-2497

Chan–Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical N-arylsulfamides

S. Won, S. Kim, Y. Kwon, I. Shin, J. Ham and W. Kim, RSC Adv., 2019, 9, 2493 DOI: 10.1039/C8RA09219B

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