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Stereoselective synthesis of the 5'-aminofuranoside part of polyoxins via (3,3)-sigmatropic rearrangement of allylic thiocyanates

Publication at First Faculty of Medicine, Faculty of Mathematics and Physics |
2001

Abstract

A new and stereospecific route for introduction of nitrogen atom at C-5 of ribose and xylose via aza-Claisen rearrangements of thiocyanates.