Organic Letters · 2007 · 17 citations · 10 references
Life SciencesBiochemistryBiocatalysisCarbohydrate ChemistryEnzymologyBiocatalytic GlycosylationCarbohydrate ProtectionCarbohydrate StructureCarbohydrate SynthesisGlycan AnalysisGlycan BiosynthesisCarbohydrate-active EnzymesEnzymatic GlycosylationEnzymatic SynthesisGlycoconjugate SynthesisGlycosylation Method DevelopmentOligosaccharide SynthesisPhotochemical ManipulationPhotochemical Reactions
The reducing end of protected carbohydrates can be equipped with a series of aglycones via the photochemical installation of a 3-mercaptoethanol linker. This linker is stable during chemical and enzymatic glycosylation reactions but can be activated readily and efficiently to couple oligosaccharides with different nucleophiles. This approach provides straightforward access to a range of molecules that serve as probes for carbohydrate modifying enzymes. [reaction: see text].
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