Won, Suk-Young Kim, Seo-Eun Kwon, Yong-Ju Shin, Inji Ham, Jungyeob Kim, Won-Suk 2024-01-19T21:01:56Z 2024-01-19T21:01:56Z 2021-09-02 2019-01-23 2046-2069 https://pubs.kist.re.kr/handle/201004/120454 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. English ROYAL SOC CHEMISTRY EFFICIENT SYNTHESIS SERINE PROTEASES COPPER INHIBITORS SULFONYLUREAS DERIVATIVES SULFAMIDES DESIGN ARYL Chan-Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical N-arylsulfamides Article 10.1039/c8ra09219b 1 RSC ADVANCES, v.9, no.5, pp.2493 - 2497 RSC ADVANCES 9 5 2493 2497 scie scopus 000457379300021 2-s2.0-85060623076 Chemistry, Multidisciplinary Chemistry Article EFFICIENT SYNTHESIS SERINE PROTEASES COPPER INHIBITORS SULFONYLUREAS DERIVATIVES SULFAMIDES DESIGN ARYL Chan-Lam coupling sulfamoyl azides unsymmetrical N-arylsulfamides