化学
吡咯
酰化
弗里德尔-克拉夫茨反应
氯化物
电泳剂
酰氯
药物化学
有机化学
催化作用
作者
Erin T. Pelkey,Gordon W. Gribble
摘要
A pyrrole and two pyrroloindoles that are substituted with a p-toluenesulfonyl group undergo an ipso acylation – detosylation reaction with acid chlorides and aluminum chloride to afford the corresponding acyl-substituted pyrroles and pyrroloindoles.Key words: pyrrole, pyrroloindole, ipso acylation, detosylation, Friedel–Crafts reaction.
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