氰化
化学
芳基
钯
位阻效应
催化作用
组合化学
硫黄
基质(水族馆)
有机化学
药物化学
海洋学
地质学
烷基
作者
Adam F. Littke,Maxime Soumeillant,Robert F. Kaltenbach,Robert J. Cherney,Christine M. Tarby,Susanne Kiau
出处
期刊:Organic Letters
[American Chemical Society]
日期:2007-03-27
卷期号:9 (9): 1711-1714
被引量:137
摘要
[reaction: see text] New methods for the palladium-catalyzed cyanation of aryl and heteroaryl chlorides have been developed, featuring sterically demanding, electron-rich phosphines. Highly challenging electron-rich aryl chlorides, in addition to electron-neutral and electron-deficient substrates, as well as nitrogen- and sulfur-containing heteroaryl chlorides can all undergo efficient cyanation under relatively mild conditions using readily available materials. In terms of substrate scope and temperature, these methods compare very favorably with the state-of-the-art cyanations of aryl chlorides.
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