Bulletin of the Chemical Society of Japan · 1986 · 21 citations · 3 references
PharmacyBiochemistryCarbohydrate ChemistryCarbohydrate SynthesisGlycan BiosynthesisGlycopyranose StereochemistryGlycoside SynthesisStereochemistry Of Sugar DerivativesStereoselective GlycosylationStereoselective Sugar Synthesis
Abstract Optically active pseudo-α-glucopyranoses have been synthesized from enantiomeric (1,3,5/2,4)-2,3-diacetoxy-4,5-dibromo-1-cyclohexanecarboxylic acids, obtained by optical resolution of the racemic modification using (+)-and (−)-α-methylbenzylamines.
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