Transition metal-catalyzed organic reactions in undivided electrochemical cells

被引:83
|
作者
Ma, Cong [1 ]
Fang, Ping [1 ]
Liu, Dong [1 ]
Jiao, Ke-Jin [1 ]
Gao, Pei-Sen [1 ]
Qiu, Hui [1 ]
Mei, Tian-Sheng [1 ]
机构
[1] Chinese Acad Sci, Univ Chinese Acad Sci, Ctr Excellence Mol Synth, Shanghai Inst Organ Chem,State Key Lab Organometa, 345 Lingling Rd, Shanghai 200032, Peoples R China
关键词
CONVERGENT PAIRED ELECTROLYSIS; C-H ALKYLATION; ASYMMETRIC HYDROCYANATION; ELECTROORGANIC CHEMISTRY; COUPLING REACTIONS; NICKEL CATALYSIS; ARYL CHLORIDES; ALPHA-PYRONES; ACTIVATION; ANNULATION;
D O I
10.1039/d1sc04011a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition metal-catalyzed organic electrochemistry is a rapidly growing research area owing in part to the ability of metal catalysts to alter the selectivity of a given transformation. This conversion mainly focuses on transition metal-catalyzed anodic oxidation and cathodic reduction and great progress has been achieved in both areas. Typically, only one of the half-cell reactions is involved in the organic reaction while a sacrificial reaction occurs at the counter electrode, which is inherently wasteful since one electrode is not being used productively. Recently, transition metal-catalyzed paired electrolysis that makes use of both anodic oxidation and cathodic reduction has attracted much attention. This perspective highlights the recent progress of each type of electrochemical reaction and relatively focuses on the transition metal-catalyzed paired electrolysis, showcasing that electrochemical reactions involving transition metal catalysis have advantages over conventional reactions in terms of controlling the reaction activity and selectivity and figuring out that transition metal-catalyzed paired electrolysis is an important direction of organic electrochemistry in the future and offers numerous opportunities for new and improved organic reaction methods.
引用
收藏
页码:12866 / 12873
页数:8
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