期刊
ADVANCED SYNTHESIS & CATALYSIS
卷 355, 期 17, 页码 3369-3374出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201300767
关键词
amidation; indole; N-fluorobenzenesulfonimide; transition metal-free reaction
资金
- National Natural Science Foundation of China [21202138]
- Xiangtan University Academic Leader Program [11QDZ20]
- New Teachers' Fund for Doctor Stations, Ministry of Education [20124301120007]
- University Student Innovation Program, Ministry of Education [201210530008]
- Hunan Provincial Natural Science Foundation [13JJ4047, 12JJ7002]
- Excellent Young Scientist Foundation of Hunan Provincial Education Department [13B114]
A direct transition metal-free regioselective C-3 amidation of indoles has been developed with the commercially available N-fluorobenzenesulfonimide (NFSI) as the amino source under external oxidant-free conditions. This amidation requires only a catalytic amount of base and exhibits excellent functional group tolerance and regioselectivity. The C-3 regioselectivity was proposed to realize by a free radical mechanism.
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