化学
芳基
弗里德尔-克拉夫茨反应
酰化
磷化氢
硼酸
钯
戒指(化学)
有机化学
组合化学
催化作用
烷基
作者
Abdol R. Hajipour,Raheleh Pourkaveh
出处
期刊:Synlett
[Thieme Medical Publishers (Germany)]
日期:2014-04-07
卷期号:25 (08): 1101-1105
被引量:9
标识
DOI:10.1055/s-0033-1341070
摘要
Palladium-catalyzed cross-coupling reaction of arylboronic acids with acid chlorides at room temperature under phosphine-free conditions affords the corresponding aromatic ketones in excellent yields within short times. This synthetic method overcomes common disadvantages of Friedel–Crafts acylation procedures and is compatible with both electron-donating and electron-withdrawing substituents on the aryl ring of the acyl chlorides.
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