Electrochemical strategies for C-H functionalization and C-N bond formation

被引:792
作者
Karkas, Markus D. [1 ]
机构
[1] KTH Royal Inst Technol, Dept Chem, Organ Chem, SE-10044 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
ELECTROLYTIC PARTIAL FLUORINATION; OLEFIN COUPLING REACTIONS; REGIOSELECTIVE ANODIC MONOFLUORINATION; NUCLEOPHILIC AROMATIC-SUBSTITUTION; BUILDING ADDRESSABLE LIBRARIES; CATION-POOL METHOD; SOLID-SUPPORTED BASES; PARALLEL LAMINAR-FLOW; ACYLIMINIUM ION POOLS; IN-SITU GENERATION;
D O I
10.1039/c7cs00619e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Conventional methods for carrying out carbon-hydrogen functionalization and carbon-nitrogen bond formation are typically conducted at elevated temperatures, and rely on expensive catalysts as well as the use of stoichiometric, and perhaps toxic, oxidants. In this regard, electrochemical synthesis has recently been recognized as a sustainable and scalable strategy for the construction of challenging carbon-carbon and carbon-heteroatom bonds. Here, electrosynthesis has proven to be an environmentally benign, highly effective and versatile platform for achieving a wide range of nonclassical bond disconnections via generation of radical intermediates under mild reaction conditions. This review provides an overview on the use of anodic electrochemical methods for expediting the development of carbon-hydrogen functionalization and carbon-nitrogen bond formation strategies. Emphasis is placed on methodology development and mechanistic insight and aims to provide inspiration for future synthetic applications in the field of electrosynthesis.
引用
收藏
页码:5786 / 5865
页数:80
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