Bulletin of the Chemical Society of Japan · 1980 · 23 citations · 7 references
Life SciencesBiochemistryChemistryCarbohydrate BiochemistryCarbohydrate ChemistryOrganic ChemistryCarbohydrate StructureGlycan AnalysisGlycan StructureMonosaccharide StereochemistryPolysaccharide StructureSugar AnalysisCarbohydrate Stereochemistry DeterminationConfigurational AnalysisConfigurational AssignmentGlycopyranose StereochemistryOligosaccharide CharacterizationPolysaccharide Structure ElucidationStereochemistry Of GlycosidesStereochemistry Of Sugar Derivatives
Abstract It was found that 13C NMR spectroscopy is applicable to the unequivocal configurational assignment at the quarternary carbon in seven pairs of 3-C-substituted-hexopyranose derivatives. The configuration of methyl 4,6-O-benzylidene-3-C-nitromethyl-2-O-p-tolylsulfonyl-α-d-glucopyranoside reported by Jordaan et al. is revised to d-allo by a chemical method.
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Satoshi Ōmura, Akira Nakagawa, András Neszmélyi et al. · Journal of the American Chemical Society · 1975 · 88 citations
The synthesis of evernitrose and 3-epi-evernitrose
Juji Yoshimura, Masafumi Matsuzawa, Kenichi Sato et al. · Carbohydrate Research · 1979 · 42 citations
Ken‐ichi Sato, Juji Yoshimura · Bulletin of the Chemical Society of Japan · 1978 · 32 citations
Momčilo Miljković, Miodrag Gligorijevic, Toshio Satoh et al. · The Journal of Organic Chemistry · 1974 · 30 citations