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Photo-induced C(sp2)-H difluoroalkylation of anilines.
Zhu, Xing-Li; Wang, Hua; Zhai, Chen-Kai; He, Wei.
Afiliación
  • Zhu XL; Department of Chemistry, School of Pharmacy, Air Force Medical University, Xi'an 710032, P.R.China. weihechem@fmmu.edu.cn.
  • Wang H; Department of Chemistry, School of Pharmacy, Air Force Medical University, Xi'an 710032, P.R.China. weihechem@fmmu.edu.cn.
  • Zhai CK; Department of Chemistry, School of Pharmacy, Air Force Medical University, Xi'an 710032, P.R.China. weihechem@fmmu.edu.cn.
  • He W; Department of Chemistry, School of Pharmacy, Air Force Medical University, Xi'an 710032, P.R.China. weihechem@fmmu.edu.cn.
Org Biomol Chem ; 22(4): 720-724, 2024 Jan 24.
Article en En | MEDLINE | ID: mdl-38165818
ABSTRACT
A photoinduced protocol for the direct difluoroalkylation of C(sp2)-H bonds in anilines under catalyst-free reaction conditions is presented. This transformation is characterized by a wide substrate scope, mild reaction conditions, and operational simplicity, and could serve as an alternative tool to established methods for the synthesis of difluoroalkylated anilines. Mechanistic studies suggest the formation of an electron-donor-acceptor (EDA) complex between anilines and difluoroalkyl bromides in this reaction.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2024 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2024 Tipo del documento: Article