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Electrochemical Nickel-Catalyzed Cross-Electrophile Coupling of Alkenyl Triflates with α-Chloroamides.
Zhang, Xi; Ye, Zenghui; Li, Yicai; Zhao, Ziqiang; Ma, Weiyuan; Zhang, Fengzhi.
Afiliação
  • Zhang X; School of Pharmacy, Hangzhou Medical College, Hangzhou, Zhejiang 310014, P. R. China.
  • Ye Z; School of Pharmacy, Hangzhou Medical College, Hangzhou, Zhejiang 310014, P. R. China.
  • Li Y; School of Pharmacy, Hangzhou Medical College, Hangzhou, Zhejiang 310014, P. R. China.
  • Zhao Z; School of Pharmacy, Hangzhou Medical College, Hangzhou, Zhejiang 310014, P. R. China.
  • Ma W; School of Pharmacy, Hangzhou Medical College, Hangzhou, Zhejiang 310014, P. R. China.
  • Zhang F; School of Pharmacy, Hangzhou Medical College, Hangzhou, Zhejiang 310014, P. R. China.
Org Lett ; 26(30): 6364-6369, 2024 Aug 02.
Article em En | MEDLINE | ID: mdl-39051850
ABSTRACT
Cross-electrophile coupling reactions of different electrophiles have been extensively studied but mainly limited to bromides and iodides. Here, we report an electrochemically induced nickel-catalyzed cross-electrophile coupling strategy between alkenyl triflates and α-chloroamides in an undivided cell under mild reaction conditions, affording the α-functionalized amide derivatives in good to excellent yields with broad substrate scopes and good functional group tolerance. The control experiments were conducted, and a plausible mechanism was proposed.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos