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作 者:Yubei Dai Fang Wang Shengqing Zhu Lingling Chu
出 处:《Chinese Chemical Letters》2022年第8期4074-4078,共5页中国化学快报(英文版)
基 金:financial support provided by the National Natural Science Foundation of China(Nos.21991123,21971036,21901036);the Shanghai Rising-Star Program(No.20QA1400200)。
摘 要:We report a Ni-catalyzed three-component cross-electrophile coupling of alkynes with alkenyl halides and fluoroalkyl halides to generate fluoroalkyl-incorporated 1,3-dienes.This mild and operationally simple protocol is distinguished by its broad substrate scope and excellent chemo-,regio-,and stereo-selectivity,offering a new and organometallic agent-free platform for the construction of fluoroalkyl-incorporated diene motifs.Preliminary mechanistic studies have been conducted to probe the potential reaction pathway.
关 键 词:FLUOROALKYLATION Cross-electrophile coupling Nickel catalysis Difunctionalization ALKYNES
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