13C nmr study of α- and β-anomeric pairs of d-mannopyranosides and l-rhamnopyranosides

Tetrahedron

Volumn 35, Issue 11, 1979, Pages 1427-1432

  Kasai, R ^a   Okihara, M ^a   Asakawa, J ^a   Mizutani, K ^a   Tanaka, O ^a  

^a HIROSHIMA UNIV SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0001168053     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(79)85038-3     Document Type: Article

References (13)

1. Determination of the absolute configuration of a secondary hydroxy group in a chiral secondary alcohol using glycosidation shifts in carbon-13 nuclear magnetic resonance spectroscopy
2. Darstellung künstlicher Antigene mit determinanten Zuckergruppen, II. Mitteil.: Synthese derp-Aminophenyl-O-α-glykoside vonL-Fucose,L-Rhamnose,D-galaktose undD-Mannose
3. Further Studies on the Assignment of Signals in13C Magnetic Resonance Spectra of Aldoses and Derived Methyl Glycosides
4. Konfigurations-, Konformations- und Substituenteneinflüsse auf die
5. A Study of 13CH Coupling Constants in Pentopyranoses and Some of their Derivatives.