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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 |
Sumario: | 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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