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Visible-Light-Induced Defluorinative α-C(sp3)-H Alkylation for the Synthesis of gem-Difluoroallylated α-Trifluoromethylamines.
Chen, Bingran; Chen, Qinlin; Liu, Yang; Chen, Jinxiu; Zhou, Xi; Wang, Haifeng; Yan, Qiongjiao; Wang, Wei; Cai, Zeyu; Chen, Fen-Er.
Affiliation
  • Chen B; Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, P. R. China.
  • Chen Q; Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, P. R. China.
  • Liu Y; Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, P. R. China.
  • Chen J; Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, P. R. China.
  • Zhou X; Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, P. R. China.
  • Wang H; Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, P. R. China.
  • Yan Q; Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, P. R. China.
  • Wang W; Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, P. R. China.
  • Cai Z; Hubei Duorui Pharmaceutical Co., Ltd. Wuhan 430205, P. R. China.
  • Chen FE; Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, P. R. China.
Org Lett ; 25(51): 9124-9129, 2023 Dec 29.
Article de En | MEDLINE | ID: mdl-37976410
ABSTRACT
Herein, we describe a novel and efficient photoredox catalytic Cα radical addition/defluoroalkylation coupling reaction between α-trifluoromethyl alkenes and N-trifluoroethyl hydroxylamine. A series of gem-difluoroallylated α-trifluoromethylamines were synthesized by the Cα radical addition enabled by a 1,2-H shift of the in situ-generated N-trifluoroethyl radical. Notably, this protocol is distinguished by its mild conditions, easy operation, and excellent functional group tolerability.

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Org Lett Sujet du journal: BIOQUIMICA Année: 2023 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Org Lett Sujet du journal: BIOQUIMICA Année: 2023 Type de document: Article