化学
芳基
区域选择性
组合化学
阴极保护
激进的
电子转移
光化学
有机化学
催化作用
烷基
电化学
电极
物理化学
作者
Bo Yang,Ming Hu,Chao Hu,Fu‐Jin Sun,Jin‐Heng Li
出处
期刊:Organic Letters
[American Chemical Society]
日期:2025-10-07
卷期号:27 (41): 11638-11643
被引量:2
标识
DOI:10.1021/acs.orglett.5c03768
摘要
An electroreduction method for regioselective 1,4-hydro(deutero)arylation of 1,3-enynes with aryl iodides and H2O or D2O has been developed, delivering diverse aryl-functionalized trisubstituted allenes under mild, transition-metal-free, and external reductant-free conditions. Upon the activation of terephthalonitrile as the organic electron transfer mediator, the protocol enables the formation of aryl radicals via single-electron transfer (SET) reduction with aryl iodides. The protocol shows a broad substrate scope with a good functional group compatibility and allows deuterium labeling using D2O with up to 99% D-incorporation. Mechanistic studies support a cathodic radical anion-single electron reduction-cathodic radical polar crossover relay pathway, offering a sustainable approach to access trisubstituted allenes.
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