Recent advances in the electrochemical generation of 1,3-dicarbonyl radicals from C-H bonds

被引:76
|
作者
Wan, Qinhui [1 ,2 ,3 ]
Zhang, Zhongyi [1 ,2 ,3 ]
Hou, Zhong-Wei [1 ,2 ]
Wang, Lei [1 ,2 ,3 ,4 ]
机构
[1] Taizhou Univ, Adv Res Inst, Jiaojiang 318000, Zhejiang, Peoples R China
[2] Taizhou Univ, Sch Pharmaceut Sci, Jiaojiang 318000, Zhejiang, Peoples R China
[3] Huaibei Normal Univ, Dept Chem, Huaibei 235000, Anhui, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Organ Chem, 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
ENANTIOSELECTIVE FLUORINATION; CATALYSIS; FUNCTIONALIZATION; OXINDOLES; ELECTROSYNTHESIS; SUBSTITUTION; ANNULATION; OXIDATION; STRATEGY; REAGENT;
D O I
10.1039/d3qo00408b
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Electrochemistry, which employs electrons as reagents and avoids the use of traditional redox reagents, becomes a powerful tool in oxidative dehydrogenation cross-coupling reactions. 1,3-Dicarbonyl derivatives are common and easily available synthetic blocks and are widely used for the construction of active molecules in organic synthesis. 1,3-Dicarbonyl radicals can be generated by direct anodic oxidation or indirect anodic oxidation with the assistance of a redox reagent and can undergo addition to arenes, double bonds or triple bonds to build multifarious organic molecules. In this review, we succinctly summarize the recent advances in the electrochemical generation of 1,3-dicarbonyl radicals from C-H-based 1,3-dicarbonyl derivatives and focus on the mechanistic insights and synthetic applications of these methods and transformations.
引用
收藏
页码:2830 / 2848
页数:19
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