4.7 Article

Transition Metal-Free Regioselective C-3 Amidation of Indoles with N-Fluorobenzenesulfonimide

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

  1. National Natural Science Foundation of China [21202138]
  2. Xiangtan University Academic Leader Program [11QDZ20]
  3. New Teachers' Fund for Doctor Stations, Ministry of Education [20124301120007]
  4. University Student Innovation Program, Ministry of Education [201210530008]
  5. Hunan Provincial Natural Science Foundation [13JJ4047, 12JJ7002]
  6. Excellent Young Scientist Foundation of Hunan Provincial Education Department [13B114]

向作者/读者索取更多资源

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.

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