Electrosynthetic C-O Bond Activation in Alcohols and Alcohol Derivatives

被引:44
|
作者
Villo, Piret [1 ]
Shatskiy, Andrey [1 ]
Karkas, Markus D. [1 ]
Lundberg, Helena [1 ]
机构
[1] KTH Royal Inst Technol, Dept Chem, SE-10044 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Alcohol; C-O Bond Activation; Cathodic Reduction; Deoxygenative; Electrosynthesis; CARBON-OXYGEN BOND; INDIRECT ELECTROCHEMICAL REDUCTION; ALLYL TRANSFER-REACTION; PALLADIUM-CATALYZED CARBOXYLATION; CATHODIC CLEAVAGE; ELECTROGENERATED NICKEL; ELECTROORGANIC REACTIONS; ELECTRON-TRANSFER; ELECTROREDUCTIVE CLEAVAGE; ORGANIC ELECTROSYNTHESIS;
D O I
10.1002/anie.202211952
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Alcohols and their derivatives are ubiquitous and versatile motifs in organic synthesis. Deoxygenative transformations of these compounds are often challenging due to the thermodynamic penalty associated with the cleavage of the C-O bond. However, electrochemically driven redox events have been shown to facilitate the C-O bond cleavage in alcohols and their derivatives either through direct electron transfer or through the use of electron transfer mediators and electroactive catalysts. Herein, a comprehensive overview of preparative electrochemically mediated protocols for C-O bond activation and functionalization is detailed, including direct and indirect electrosynthetic methods, as well as photoelectrochemical strategies.
引用
收藏
页数:28
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