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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...

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Detalles Bibliográficos
Autores principales: Cowper, Paul, Jin, Yu, Turton, Michael D., Kociok‐Köhn, Gabriele, Lewis, Simon E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
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.
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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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