Synthesis 2015; 47(19): 2912-2923
DOI: 10.1055/s-0035-1560457
feature
© Georg Thieme Verlag Stuttgart · New York

Palladium-Catalyzed Heck-Type Difluoroalkylation of Alkenes with Functionalized Difluoromethyl Bromides

Feng Zhang
Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, P. R. of China   Email: xgzhang@mail.sioc.ac.cn
,
Qiao-Qiao Min
Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, P. R. of China   Email: xgzhang@mail.sioc.ac.cn
,
Xingang Zhang*
Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, P. R. of China   Email: xgzhang@mail.sioc.ac.cn
› Author Affiliations
Further Information

Publication History

Received: 02 July 2015

Accepted after revision: 27 July 2015

Publication Date:
17 August 2015 (online)


Abstract

An efficient method for the synthesis of difluoroalkylated alkenes through palladium-catalyzed Heck-type reaction with functionalized difluoromethyl bromides has been developed. The advantages of this protocol are its synthetic simplicity, excellent functional group compatibility, and efficient late-stage difluoroalkylation of biologically relevant molecules, thus paving a new way for application in drug discovery and development. Mechanistic studies revealed that the free difluoroalkyl radicals, initiated by a [Pd(0)Ln] via a single-electron-transfer (SET) pathway, were involved in the Heck-type catalytic cycle.

Supporting Information