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Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross‐Coupling
Azulenesulfonium salts may be readily prepared from the corresponding azulenes by an S(E)Ar reaction. These azulene sulfonium salts are bench‐stable species that may be employed as pseudohalides for cross‐coupling. Specifically, their application in Suzuki–Miyaura reactions has been demonstrated wit...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4755203/ https://www.ncbi.nlm.nih.gov/pubmed/26806850 http://dx.doi.org/10.1002/anie.201510666 |
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author | Cowper, Paul Jin, Yu Turton, Michael D. Kociok‐Köhn, Gabriele Lewis, Simon E. |
author_facet | Cowper, Paul Jin, Yu Turton, Michael D. Kociok‐Köhn, Gabriele Lewis, Simon E. |
author_sort | Cowper, Paul |
collection | PubMed |
description | Azulenesulfonium salts may be readily prepared from the corresponding azulenes by an S(E)Ar reaction. These azulene sulfonium salts are bench‐stable species that may be employed as pseudohalides for cross‐coupling. Specifically, their application in Suzuki–Miyaura reactions has been demonstrated with a diverse selection of coupling partners. These azulenesulfonium salts possess significant advantages in comparison with the corresponding azulenyl halides, which are known to be unstable and difficult to prepare in pure form. |
format | Online Article Text |
id | pubmed-4755203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47552032016-02-25 Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross‐Coupling Cowper, Paul Jin, Yu Turton, Michael D. Kociok‐Köhn, Gabriele Lewis, Simon E. Angew Chem Int Ed Engl Communications Azulenesulfonium salts may be readily prepared from the corresponding azulenes by an S(E)Ar reaction. These azulene sulfonium salts are bench‐stable species that may be employed as pseudohalides for cross‐coupling. Specifically, their application in Suzuki–Miyaura reactions has been demonstrated with a diverse selection of coupling partners. These azulenesulfonium salts possess significant advantages in comparison with the corresponding azulenyl halides, which are known to be unstable and difficult to prepare in pure form. John Wiley and Sons Inc. 2016-01-14 2016-02 /pmc/articles/PMC4755203/ /pubmed/26806850 http://dx.doi.org/10.1002/anie.201510666 Text en © 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Cowper, Paul Jin, Yu Turton, Michael D. Kociok‐Köhn, Gabriele Lewis, Simon E. Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross‐Coupling |
title | Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross‐Coupling |
title_full | Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross‐Coupling |
title_fullStr | Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross‐Coupling |
title_full_unstemmed | Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross‐Coupling |
title_short | Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross‐Coupling |
title_sort | azulenesulfonium salts: accessible, stable, and versatile reagents for cross‐coupling |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4755203/ https://www.ncbi.nlm.nih.gov/pubmed/26806850 http://dx.doi.org/10.1002/anie.201510666 |
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