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Arylation and Heteroarylation of Thienylsulfonamides with Organotrifluoroborates
[Image: see text] A mild, practical protocol has been developed for the Suzuki cross-coupling of unprotected thienylsulfonamides from air- and bench-stable organotrifluoroborates in the absence of a protecting group on the sulfonamide nitrogen. The developed synthetic method can be applied to the pr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4120984/ https://www.ncbi.nlm.nih.gov/pubmed/25019222 http://dx.doi.org/10.1021/jo501323z |
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author | Noreen, Mnaza Rasool, Nasir El Khatib, Mirna Molander, Gary A. |
author_facet | Noreen, Mnaza Rasool, Nasir El Khatib, Mirna Molander, Gary A. |
author_sort | Noreen, Mnaza |
collection | PubMed |
description | [Image: see text] A mild, practical protocol has been developed for the Suzuki cross-coupling of unprotected thienylsulfonamides from air- and bench-stable organotrifluoroborates in the absence of a protecting group on the sulfonamide nitrogen. The developed synthetic method can be applied to the preparation of various arylated and heteroarylated thienylsulfonamides under conditions that are tolerant of a broad range of functional groups. |
format | Online Article Text |
id | pubmed-4120984 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-41209842015-07-14 Arylation and Heteroarylation of Thienylsulfonamides with Organotrifluoroborates Noreen, Mnaza Rasool, Nasir El Khatib, Mirna Molander, Gary A. J Org Chem [Image: see text] A mild, practical protocol has been developed for the Suzuki cross-coupling of unprotected thienylsulfonamides from air- and bench-stable organotrifluoroborates in the absence of a protecting group on the sulfonamide nitrogen. The developed synthetic method can be applied to the preparation of various arylated and heteroarylated thienylsulfonamides under conditions that are tolerant of a broad range of functional groups. American Chemical Society 2014-07-14 2014-08-01 /pmc/articles/PMC4120984/ /pubmed/25019222 http://dx.doi.org/10.1021/jo501323z Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Noreen, Mnaza Rasool, Nasir El Khatib, Mirna Molander, Gary A. Arylation and Heteroarylation of Thienylsulfonamides with Organotrifluoroborates |
title | Arylation and Heteroarylation
of Thienylsulfonamides
with Organotrifluoroborates |
title_full | Arylation and Heteroarylation
of Thienylsulfonamides
with Organotrifluoroborates |
title_fullStr | Arylation and Heteroarylation
of Thienylsulfonamides
with Organotrifluoroborates |
title_full_unstemmed | Arylation and Heteroarylation
of Thienylsulfonamides
with Organotrifluoroborates |
title_short | Arylation and Heteroarylation
of Thienylsulfonamides
with Organotrifluoroborates |
title_sort | arylation and heteroarylation
of thienylsulfonamides
with organotrifluoroborates |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4120984/ https://www.ncbi.nlm.nih.gov/pubmed/25019222 http://dx.doi.org/10.1021/jo501323z |
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