酰化
化学
氯化物
反应条件
酰氯
有机化学
酰基
药物化学
苯甲酰氯
群(周期表)
催化作用
作者
Tatsuo Okauchi,Masaaki Itonaga,Toru Minami,Takashi Owa,Kyosuke Kitoh,Hiroshi Yoshino
出处
期刊:Organic Letters
[American Chemical Society]
日期:2000-04-27
卷期号:2 (10): 1485-1487
被引量:150
摘要
[reaction--see text] Indoles are selectively acylated at the 3-position in high yields on treatment with a wide variety of acyl chlorides in CH(2)Cl(2) in the presence of diethylaluminum chloride or dimethylaluminum chloride. The reaction proceeds under mild conditions and is applicable to indoles bearing various functional groups without NH protection.
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