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摘要
An efficient and high-yielding, one-pot, Cu-catalyzed synthesis of 2-indolyl-C-glycosides is delineated. The sequence involves a cascade Sonogashira type coupling and a hydroamination reaction between sugar-derived alkynes and N-tosyl-o-iodoaniline followed by removal of the N-tosyl group to provide a library of 2-indolyl-C-glycosides in moderate to excellent yields.
- 出版日期2013-1
