ChemInform Abstract: Direct Glycosylations with 1-Hydroxy Glycosyl Donors Using Trifluoromethanesulfonic Anhydride and Diphenyl Sulfoxide.
Abstract
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ChemInform Abstract
A new method for glycosidic bond construction is described involving in situ activation of the anomeric hydroxyl. This one-step procedure is applicable directly to the glycosylation of a wide range of acceptors. The C-2 neighboring group effects the glycosylation stereochemistry. In the case of (XII) β-selectivity is observed exclusively.