Organic Letters · 2004 · 87 citations · 7 references
Life SciencesBiochemistryCarbohydrate ChemistryCarbohydrate SynthesisGlycosidic Bond FormationGlycosylation PathwaysMonosaccharide ChemistryN-linked GlycosylationProtein GlycosylationChemoselective Glycosidic Bond FormationOligosaccharide SynthesisOne-pot GlycosylationOne-pot Oligosaccharide SynthesisRoom-temperature Synthesis
N-(phenylthio)-epsilon-caprolactam (1) has been applied as a new promoter for the activation of thioglycosides. This proceeds by the reaction of 1 with trifluoromethansulfonic anhydride, which subsequently activates the thioglycoside for glycosidic bond formation. Notably, the reaction proceeds efficiently at room temperature and is adaptable to our reactivity-based one-pot oligosaccharide synthesis. [reaction: see text]
7