New Redox Strategies in Organic Synthesis by Means of Electrochemistry and Photochemistry

被引:353
作者
Liu, Jinjian [1 ]
Lu, Lingxiang [1 ]
Wood, Devin [1 ]
Lin, Song [1 ]
机构
[1] Cornell Univ, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
基金
美国国家卫生研究院;
关键词
C-H FUNCTIONALIZATION; LIGHT PHOTOREDOX CATALYSIS; ELECTROCATALYTIC APPROACH; ANODIC-OXIDATION; ELECTROORGANIC CHEMISTRY; DECATUNGSTATE ANION; ARYL CHLORIDES; BOND FORMATION; ION BATTERY; ELECTROSYNTHESIS;
D O I
10.1021/acscentsci.0c00549
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
As the breadth of radical chemistry grows, new means to promote and regulate single-electron redox activities play increasingly important roles in driving modern synthetic innovation. In this regard, photochemistry and electrochemistry-both considered as niche fields for decades-have seen an explosive renewal of interest in recent years and gradually have become a cornerstone of organic chemistry. In this Outlook article, we examine the current state-of-the-art in the areas of electrochemistry and photochemistry, as well as the nascent area of electrophotochemistry. These techniques employ external stimuli to activate organic molecules and imbue privileged control of reaction progress and selectivity that is challenging to traditional chemical methods. Thus, they provide alternative entries to known and new reactive intermediates and enable distinct synthetic strategies that were previously unimaginable. Of the many hallmarks, electro- and photochemistry are often classified as "green" technologies, promoting organic reactions under mild conditions without the necessity for potent and wasteful oxidants and reductants. This Outlook reviews the most recent growth of these fields with special emphasis on conceptual advances that have given rise to enhanced accessibility to the tools of the modern chemical trade.
引用
收藏
页码:1317 / 1340
页数:24
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