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Visible‐Light Photoredox‐Catalyzed C−H Difluoroalkylation of Hydrazones through an Aminyl Radical/Polar Mechanism
Author(s) -
Xu Pan,
Wang Guoqiang,
Zhu Yuchen,
Li Weipeng,
Cheng Yixiang,
Li Shuhua,
Zhu Chengjian
Publication year - 2016
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201508698
Subject(s) - chemistry , hydrazone , photochemistry , aldehyde , electron transfer , substrate (aquarium) , polar , reaction mechanism , amine gas treating , radical , catalysis , stereochemistry , organic chemistry , physics , astronomy , geology , oceanography
An unprecedented visible‐light‐induced direct C−H bond difluoroalkylation of aldehyde‐derived hydrazones was developed. This reaction represents a new way to synthesize substituted hydrazones. The salient features of this reaction include difluorinated hydrazone synthesis rather than classical amine synthesis, extremely mild reaction conditions, high efficiency, wide substrate scope, ease in further transformations of the products, and one‐pot syntheses. Mechanistic analyses and theoretical calculations indicate that this reaction is enabled by a novel aminyl radical/polar crossover mechanism, with the aminyl radical being oxidized into the corresponding aminyl cation through a single electron transfer (SET) process.