A versatile strategy for difunctionalization of carbon–carbon multiple bonds by photoredox catalysis
文献信息
发布日期
2016-05-31
DOI
10.1039/C6QO00139D
影响因子
5.281
作者
Takashi Koike, Munetaka Akita
查看原文
摘要
Photoredox catalysis has emerged as a strong synthetic tool for radical reactions. In particular, a variety of regioselective difunctionalizations of carbon–carbon multiple bonds through SET photoredox processes (oxidative quenching cycle) have been accomplished by an appropriate choice of an electrophilic radical precursor and a nucleophile. The basic concept, representative results and future prospect are the topics of this article.
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来源期刊
Organic Chemistry Frontiers
CiteScore:
7.8
自引率:
8.7%
年发文量:
724
Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry
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