Chan-Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical N-arylsulfamides
- Authors
- Won, Suk-Young; Kim, Seo-Eun; Kwon, Yong-Ju; Shin, Inji; Ham, Jungyeob; Kim, 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
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.