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Access to Sulfoxides under NHC/Photocatalysis via a Radical Pathway.
Wang, Xuefeng; Tang, Yulian; Ye, Shengqing; Zhang, Jun; Kuang, Yunyan; Wu, Jie.
Afiliação
  • Wang X; Department of Chemistry, Fudan University, 2005 Songhu Road, Shanghai 200438, China.
  • Tang Y; Department of Chemistry, Fudan University, 2005 Songhu Road, Shanghai 200438, China.
  • Ye S; School of Pharmaceutical and Materials Engineering & Institute for Advanced Studies, Taizhou University, 1139 Shifu Avenue, Taizhou 318000, China.
  • Zhang J; School of Pharmaceutical and Materials Engineering & Institute for Advanced Studies, Taizhou University, 1139 Shifu Avenue, Taizhou 318000, China.
  • Kuang Y; Department of Chemistry, Fudan University, 2005 Songhu Road, Shanghai 200438, China.
  • Wu J; School of Pharmaceutical and Materials Engineering & Institute for Advanced Studies, Taizhou University, 1139 Shifu Avenue, Taizhou 318000, China.
Org Lett ; 24(10): 2059-2063, 2022 Mar 18.
Article em En | MEDLINE | ID: mdl-35262358
ABSTRACT
A photocatalyzed transformation from sulfinic acids to sulfoxides under visible-light irradiation in the presence of N-heterocyclic carbene is established. Various alkyl groups from four-substituted Hantzsch esters or Meyer nitriles are smoothly converted to the corresponding sulfoxides through a radical coupling pathway in the presence of 1,1-carbonyldiimidazole. This method allows sulfoxide synthesis to refrain from relying on the oxidation of sulfides and provides an alternative route for the preparation of sulfoxides.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Ano de publicação: 2022 Tipo de documento: Article