Journal of Carbohydrate Chemistry · 2006 · 12 citations · 20 references
PharmacyBiochemistryCarbohydrate BiochemistryCarbohydrate ChemistryGlycobiologyCarbohydrate DeprotectionCarbohydrate ProtectionCarbohydrate StructureCarbohydrate SynthesisProtecting-group StrategySafer Chemical SynthesisAmino Acid Protection ChemistryAmino Protecting GroupsCarbohydrate Building Block SynthesisOligosaccharide SynthesisProtecting Group ChemistrySelective Deprotection
Oligosaccharide synthesis using aminosugars requires the presence of a suitable amino protecting group. A number of protecting groups are currently used, and while many display favorable properties, most agents available still suffer from certain disadvantages. This report details the use of a hydrazine labile aminosugar protecting group, N‐[1‐(4,4‐dimethyl‐2,6‐dioxocyclohex‐1‐ylidene)ethyl] (Dde), which can be introduced and removed in a facile and cost‐effective manner.
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