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

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 sulfamid...

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Autores principales: Won, Suk-Young, Kim, Seo-Eun, Kwon, Yong-Ju, Shin, Inji, Ham, Jungyeob, Kim, Won-Suk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059883/
https://www.ncbi.nlm.nih.gov/pubmed/35520509
http://dx.doi.org/10.1039/c8ra09219b
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author Won, Suk-Young
Kim, Seo-Eun
Kwon, Yong-Ju
Shin, Inji
Ham, Jungyeob
Kim, Won-Suk
author_facet Won, Suk-Young
Kim, Seo-Eun
Kwon, Yong-Ju
Shin, Inji
Ham, Jungyeob
Kim, Won-Suk
author_sort Won, Suk-Young
collection PubMed
description 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.
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spelling pubmed-90598832022-05-04 Chan–Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical N-arylsulfamides Won, Suk-Young Kim, Seo-Eun Kwon, Yong-Ju Shin, Inji Ham, Jungyeob Kim, Won-Suk RSC Adv Chemistry 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. The Royal Society of Chemistry 2019-01-18 /pmc/articles/PMC9059883/ /pubmed/35520509 http://dx.doi.org/10.1039/c8ra09219b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Won, Suk-Young
Kim, Seo-Eun
Kwon, Yong-Ju
Shin, Inji
Ham, Jungyeob
Kim, Won-Suk
Chan–Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical N-arylsulfamides
title Chan–Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical N-arylsulfamides
title_full Chan–Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical N-arylsulfamides
title_fullStr Chan–Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical N-arylsulfamides
title_full_unstemmed Chan–Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical N-arylsulfamides
title_short Chan–Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical N-arylsulfamides
title_sort chan–lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical n-arylsulfamides
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059883/
https://www.ncbi.nlm.nih.gov/pubmed/35520509
http://dx.doi.org/10.1039/c8ra09219b
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