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A synthetic guide to alkynyl sulfides.
Santandrea, Jeffrey; Godin, Eric; Collins, Shawn K.
Afiliação
  • Santandrea J; Department of Chemistry and Centre in Green Chemistry and Catalysis, Université de Montréal, CP 6128 Station Downtown, Montréal, Québec, CanadaH3C 3J7. shawn.collins@umontreal.ca.
  • Godin E; Department of Chemistry and Centre in Green Chemistry and Catalysis, Université de Montréal, CP 6128 Station Downtown, Montréal, Québec, CanadaH3C 3J7. shawn.collins@umontreal.ca.
  • Collins SK; Department of Chemistry and Centre in Green Chemistry and Catalysis, Université de Montréal, CP 6128 Station Downtown, Montréal, Québec, CanadaH3C 3J7. shawn.collins@umontreal.ca.
Org Biomol Chem ; 18(26): 4885-4893, 2020 07 08.
Article em En | MEDLINE | ID: mdl-32538415
ABSTRACT
The relative stability and predictable reactivity of alkynyl sulfides make them ideal synthons for the development of new transformations. Classic methods for forming alkynyl sulfides relied on dehydrohalogenation approaches. However more recent methods have focused on employing umpolung strategies, as well as nucleophilic and electrophilic thiol alkynylation. In addition, the recent syntheses of Csp-S bonds have trended towards exploiting catalysis and expanding the reaction scope of the methods. A survey of existing methods to form alkynyl sulfides is presented as well as an evaluation with regards to the scope of each method, to provide the reader with an overview of advantages and limitations of current technology.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article