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Metal-Free Chemoselective S-Arylation of Sulfenamides To Access Sulfilimines.
Wu, Xianda; Li, Yuqing; Chen, Minghong; He, Fu-Sheng; Wu, Jie.
Afiliação
  • Wu X; Jiangxi Key Laboratory of Organic Chemistry, Jiangxi Science and Technology Normal University, Nanchang 330013, China.
  • Li Y; School of Pharmaceutical and Chemical Engineering and Institute for Advanced Studies, Taizhou University, Taizhou, Zhejiang 3180000, China.
  • Chen M; School of Pharmaceutical and Chemical Engineering and Institute for Advanced Studies, Taizhou University, Taizhou, Zhejiang 3180000, China.
  • He FS; School of Pharmaceutical and Chemical Engineering and Institute for Advanced Studies, Taizhou University, Taizhou, Zhejiang 3180000, China.
  • Wu J; School of Pharmaceutical and Chemical Engineering and Institute for Advanced Studies, Taizhou University, Taizhou, Zhejiang 3180000, China.
J Org Chem ; 88(13): 9352-9359, 2023 Jul 07.
Article em En | MEDLINE | ID: mdl-37327035
ABSTRACT
A novel and efficient S-arylation of sulfenamides with diaryliodonium salts for the synthesis of sulfilimines is developed. The reaction proceeds smoothly under transition-metal-free and air conditions, giving rapid access to sulfilimines in good to excellent yields via selective S-C bond formation. This protocol is scalable and exhibits a broad substrate scope, good functional group tolerance, and excellent chemoselectivity.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Elementos de Transição / Metais Idioma: En Revista: J Org Chem Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Elementos de Transição / Metais Idioma: En Revista: J Org Chem Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China