Assignment of Anomeric Configuration and Identification of Carbohydrate Residues by13C NMR: Arabino- and Ribopyranosides and Furancsides
- 1 January 1984
- journal article
- research article
- Published by Taylor & Francis in Journal of Carbohydrate Chemistry
- Vol. 3 (2) , 253-266
- https://doi.org/10.1080/07328308408058819
Abstract
A 13C NMR fingerprint method previously developed for galactosides and glucosides is extended to arabinosides and ribosides. This approach demonstrates the capability of 13C NMR to determine ring size and anomeric configuration in four isomeric arabinosides and ribosides.This publication has 17 references indexed in Scilit:
- Assignment of anomeric configuration and identification of carbohydrate residues by 13C nmr. 1. Galacto- and glucopyranosides and furanosidesCanadian Journal of Chemistry, 1980
- 13C-N.M.R. Spectroscopy of α- and β-anomeric series of alkyl l-arabinopyranosidesCarbohydrate Research, 1980
- Determination of the absolute configuration of a secondary hydroxy group in a chiral secondary alcohol using glycosidation shifts in carbon-13 nuclear magnetic resonance spectroscopyJournal of the American Chemical Society, 1978
- Carbon-13 NMR studies of flavonoids—IIITetrahedron, 1978
- Carbon-13 and proton nuclear magnetic resonance studies on methyl aldofuranosides and their O-alkyl derivativesCarbohydrate Research, 1976
- Carbon-13 Chemical Shifts of Furanosides and Cyclopentanols. Configurational and Conformational InfluencesCanadian Journal of Chemistry, 1975
- Further Studies on the Assignment of Signals in 13C Magnetic Resonance Spectra of Aldoses and Derived Methyl GlycosidesCanadian Journal of Chemistry, 1975
- A Study of 13CH Coupling Constants in Pentopyranoses and Some of their Derivatives.Acta Chemica Scandinavica, 1975
- Konfigurations- und konformations- untersuchungen von adenosinanalogen mit 13C-ResonanzTetrahedron, 1973
- Konfigurations‐, Konformations‐ und Substituenteneinflüsse auf dieEuropean Journal of Inorganic Chemistry, 1971