## Abstract Peracetyl derivatives of oligo‐ and polysaccharides showed their own characteristic acetate‐methyl signals in the NMR spectra measured in chloroform‐__d__, which are useful for the identification and conformational analysis of oligo‐ and polysaccharides in solutions. An acetate‐methyl s
Acetate-methyl signals in the NMR spectra of peracetylated derivatives of chondroitin sulfates and their desulfated derivatives
✍ Scribed by Shigehiro Hirano
- Publisher
- John Wiley and Sons
- Year
- 1970
- Tongue
- English
- Weight
- 370 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Chondroitin 4‐sulfate (Ch4S), chondroitin 6‐sulfate (Ch6S), dermatan sulfate, chondroitin and desulfated dermatan sulfate were peracetylated and the derivatives isolated in yields of 45 to 88%. Acetate‐methyl signals in the NMR spectra of these derivatives in D~2~O were analyzed using a correlation of the chemical shifts to the orientations. The lC conformation of hexopyranosiduronic acid moieties was estimated in these derivatives. No significant change of the chemical shifts was observed with the NMR spectra measured in D~2~O, in 7 M urea solution, in the various diluted solutions, and in the temperature range of 2 to 95° in D~2~O.
📜 SIMILAR VOLUMES
## Abstract Acylation of allyl alcohols induces strong carbon shifts, shielding γ and deshielding δ effects. These shifts are a consequence of through‐bond polarization of the olefinic carbons. Allyl ethers show similar, but milder perturbations. The olefinic carbon shifts reveal a strong concentra
## Abstract The 1,4‐dioxane‐2,3‐diols and a number of their methyl‐substituted derivatives were synthesized and their ^13^C NMR spectra measured. The configurational properties were studied on the basis of the spectral data and chemical equilibration. For the parent compound the __trans__ configura
## Abstract For Abstract see ChemInform Abstract in Full Text.