期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 77, 期 22, 页码 10382-10392出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo302112a
关键词
-
资金
- Department of Science and Technology, New Delhi, India
- University of Delhi
- Council of Scientific and Industrial Research, New Delhi, India
An operationally simple approach for the regioselective tandem synthesis of indolo[1,2-a]quinolines 4a-v and pyrrolo[1,2-a]quinolines 5a-k from 1-(2-bromophenyl)-1H-indole/pyrrole/imidazole 1a-c, 2a,b by the palladium-catalyzed sequential C-C bond formation is described. The developed approach involves the palladium-catalyzed Sonogashira coupling followed by the intramolecular C-C bond formation via C-H activation, which leads to the formation of 6-endo-dig cyclized product. This synthetic methodology accommodates wide functional group variation on alkyne, which proves to be advantageous for the structural and biological activity assessments.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据