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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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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. |
format | Online Article Text |
id | pubmed-9059883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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