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Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zu Chong Zhi Road, Zhangjiang Hi-Tech Park, Shanghai 201203, PR China
E-mail: zhoubing2012@hotmail.com
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; Tel: (+) 86 21 50807288
Org. Biomol. Chem., 2012,10, 8953-8955
DOI:
10.1039/C2OB26767E
Received
07 Sep 2012,
Accepted
05 Oct 2012
First published online
09 Oct 2012
Direct C-2 amidation of indoles was reported using sulfonyl azides as the amino source to release N2 as the single byproduct. This reaction exhibits high functional group tolerance and regioselectivity, providing a variety of 2-amino substituted indoles in high to excellent yield. The procedure is robust, reliable, and compatible with water and air.
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Organic & Biomolecular Chemistry
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