Rhodaelectro-Catalyzed C–H and C–C Activation  被引量:2

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作  者:Youai Qiu Cuiju Zhu Maximilian Stangier Julia Struwe Lutz Ackermann 

机构地区:[1]Institut für Organische und Biomolekulare Chemie,Georg-August-Universität Göttingen,Göttingen 37077

出  处:《CCS Chemistry》2021年第2期1529-1552,共24页中国化学会会刊(英文)

基  金:support by the Deutsche Forschungsgemeinschaft(German Research Foundation)(Gottfried-Wilhelm-Leibniz award to L.A.)and the China Scholarship Council(fellowship to C.Z.)is gratefully acknowledged.

摘  要:Rhodium(III)catalysis has set the stage for a plethora of oxidative C–H functionalizations over the last decade,which have predominantly employed stoichiometric amounts of toxic and expensive metal oxidants,such as silver(I)salts.In the meantime,electrosynthesis has emerged as an increasingly viable alternative for expensive and toxic oxidants.Recently,significant momentum has been achieved with the merger of electrocatalysis with organometallic C–H activation.However,user-friendly and robust rhodaelectro-catalysis has until very recently proven elusive for oxidative C–H activations.This minireview highlights the current knowledge and recent advances of electrooxidation in rhodium-catalyzed C–H or C–C activations,with a topical focus on contributions from the Ackermann group through July 2020.

关 键 词:ELECTROSYNTHESIS rhodium catalysis C–H activation C–C activation mechanistic in-sights rhodaelectro-catalysis 

分 类 号:O64[理学—物理化学]

 

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