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Azulenesulfonium Salts: Accessible, Stable, and Versatile Reagents for Cross-Coupling.
Cowper, Paul; Jin, Yu; Turton, Michael D; Kociok-Köhn, Gabriele; Lewis, Simon E.
Afiliação
  • Cowper P; Department of Chemistry, University of Bath, Bath, BA2 7AY, UK. p.cowper@bath.ac.uk.
  • Jin Y; Department of Chemistry, University of Bath, Bath, BA2 7AY, UK.
  • Turton MD; Department of Chemistry, University of Bath, Bath, BA2 7AY, UK.
  • Kociok-Köhn G; Chemical Characterisation and Analysis Facility, University of Bath, Bath, BA2 7AY, UK.
  • Lewis SE; Department of Chemistry, University of Bath, Bath, BA2 7AY, UK. s.e.lewis@bath.ac.uk.
Angew Chem Int Ed Engl ; 55(7): 2564-8, 2016 Feb 12.
Article em En | MEDLINE | ID: mdl-26806850
ABSTRACT
Azulenesulfonium salts may be readily prepared from the corresponding azulenes by an SE 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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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article