Electrochemical Oxidation Induced Selective C-C Bond Cleavage

被引:327
|
作者
Shi, Shi-Hui [1 ,2 ]
Liang, Yujie [1 ]
Jiao, Ning [1 ,3 ]
机构
[1] Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
[2] Yanan Univ, Coll Chem & Chem Engn, Shaanxi Key Lab Chem React Engn, Yanan 716000, Shaanxi, Peoples R China
[3] Chinese Acad Sci, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
NON-KOLBE ELECTROLYSIS; ANODIC-OXIDATION; ELECTROORGANIC CHEMISTRY; SYNTHETIC APPLICATIONS; CARBOXYLIC-ACIDS; CINNAMIC-ACIDS; METHYL KETONES; CARBON BOND; ELECTROSYNTHESIS; DECARBOXYLATION;
D O I
10.1021/acs.chemrev.0c00335
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Selective C-C bond cleavage under mild conditions can serve as a valuable tool for organic syntheses and macromolecular degradation. However, the conventional chemical methods have largely involved the use of noble transition-metal catalysts as well as the stoichiometric and perhaps environmentally unfriendly oxidants, compromising the overall sustainable nature of C-C transformation chemistry. In this regard, electrochemical C-C bond cleavage has been identified as a sustainable and scalable strategy that employs electricity to replace byproduct-generating chemical reagents. To date, the progress made in this area has mainly relied on Kolbe electrolysis and related processes. Encouragingly, more and more examples of the cleavage of C-C bonds via other maneuvers have recently been developed. This review provides an overview on the most recent and significant developments in electrochemically oxidative selective C-C bond cleavage, with an emphasis on both synthetic outcomes and reaction mechanisms, and it showcases the innate advantages and exciting potentials of electrochemical synthesis.
引用
收藏
页码:485 / 505
页数:21
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