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作 者:Yuan-Qiong Huang Zhi-Jie Wu Li Zhu Qing Gu Xiaojie Lu Shu-Li You Tian-Sheng Mei
机构地区:[1]State Key Laboratory of Organometallic Chemistry,Center for Excellence in Molecular Synthesis,Shanghai Institute of Organic Chemistry,University of Chinese Academy of Sciences,Chinese Academy of Sciences,Shanghai 200032 [2]State Key Laboratory of Drug Research,Shanghai Institute of Materia Medica,Chinese Academy of Sciences,Pudong,Shanghai 201203
出 处:《CCS Chemistry》2022年第9期3181-3189,共9页中国化学会会刊(英文)
基 金:grant fromNSFC(nos.21821002,21772222,and 91956112),CAS(no.XDB20000000);Science and Technology Commission of Shanghai Municipality(nos.18JC1415600 and 20JC1417100).
摘 要:The synergistic use of transition metal catalysis and electrochemistry is an attractive strategy for oxidative site-selective C–H functionalization since the use of stoichiometric chemical oxidants can be avoided and novel reactivity can be achieved.However,metalcatalyzed electrochemical C–H functionalization is mainly limited to arene C(sp^(2))–Hfunctionalization,and enantioselective C–H functionalization is uncommon and remains challenging.
关 键 词:organic electrochemistry enantioselective C–H annulation rhodium catalysis chiral spiropyrazolones C–H functionalization
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