Journal of Carbohydrate Chemistry · 1990 · 21 citations · 3 references
PharmacyChemistryCarbohydrate ChemistryOrganic ChemistryCarbohydrate ReactivityCarbohydrate SynthesisCarbohydrate-derived Natural ProductsGlycosidic Bond FormationHeterocyclic ChemistryC-glycoside SynthesisCarbohydrate Building Block SynthesisMild Reaction ConditionsStability Under Reaction ConditionsStereochemistry Of Sugar DerivativesStereoselective Sugar Synthesis
ABSTRACT ABSTRACT Cyclopentylidene ketals, moderately more acid-labile than their isopropylidene analogs, offer an alternative to the latter blocking groups. They have been shown to resist a large variety of reaction conditions commonly encountered in carbohydrate chemistry.
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DERIVATIVES OF MONOACETONE XYLOSE
P.A. Levene, Albert L. Raymond · Journal of Biological Chemistry · 1933 · 102 citations · Full text
Terminal Deoxy Hydroxyamino Sugars
Jean M. J. Tronchet, Guido Zosimo‐Landolfo, N. Bizzozero et al. · Journal of Carbohydrate Chemistry · 1988 · 26 citations