氮杂环丁烷
氮丙啶
化学
钯
催化作用
芳基
偶联反应
有机化学
戒指(化学)
组合化学
劈理(地质)
药物化学
断裂(地质)
工程类
岩土工程
烷基
作者
B. Witulski,Stefan Senft,Jordi Bonet,Jan Oliver Jost
出处
期刊:Synthesis
[Georg Thieme Verlag KG]
日期:2007-01-01
卷期号:2007 (2): 243-250
被引量:13
标识
DOI:10.1055/s-2006-958947
摘要
Studies on the viability of palladium-catalyzed cross-coupling reactions of aryl- or hetaryl bromides with the parent aziridine or azetidine showed that a wide range of N-arylaziridines and N-arylazetidines are accessible by this method. Ring cleavage of the N-arylaziridines or -azetidines thus produced does not occur under the applied reaction conditions. The synthetic utility of the method is illustrated by examples of double N-arylations with either aziridine or azetidine.
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