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

Authors
Won, Suk-YoungKim, Seo-EunKwon, Yong-JuShin, InjiHam, JungyeobKim, Won-Suk
Issue Date
2019-01-23
Publisher
ROYAL SOC CHEMISTRY
Citation
RSC ADVANCES, v.9, no.5, pp.2493 - 2497
Abstract
An efficient method was developed for the synthesis of unsymmetrical N-arylsulfamides using sulfamoyl azides and arylboronic acids in the presence of 10mol% 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.
Keywords
EFFICIENT SYNTHESIS; SERINE PROTEASES; COPPER; INHIBITORS; SULFONYLUREAS; DERIVATIVES; SULFAMIDES; DESIGN; ARYL; EFFICIENT SYNTHESIS; SERINE PROTEASES; COPPER; INHIBITORS; SULFONYLUREAS; DERIVATIVES; SULFAMIDES; DESIGN; ARYL; Chan-Lam coupling; sulfamoyl azides; unsymmetrical N-arylsulfamides
ISSN
2046-2069
URI
https://pubs.kist.re.kr/handle/201004/120454
DOI
10.1039/c8ra09219b
Appears in Collections:
KIST Article > 2019
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE