Synthesis and transformations of d-glucuronic and l-iduronic acid glycals
โ Scribed by Peter Schell; Hernan A Orgueira; Susanne Roehrig; Peter H Seeberger
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 92 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
D-Glucuronic acid glycals can be efficiently synthesized from diacetone glucose or tri-O-acetyl glycal and can be transformed into D-glucuronic acid donors and acceptors in high yields. Base catalyzed epimerization of D-glucuronic acid glycals provides access to the corresponding L-iduronic acid glycals. Both D-glucuronic and L-iduronic acid glycals were transformed into glycosylating agents for use in the synthesis of glycosaminoglycan oligosaccharides.
๐ SIMILAR VOLUMES
A gas chromatographic procedure has been developed for the analysis of uranic acids as aldonic acid butaneboronates. With these derivatives, aldoses frequently accompanying uranic acids in polysaccharide hydrolyzates are readily separated and measured. The method has been applied to the assay of idu
A new electrophoretic method using Titan III cellulose acetate plates has been developed for the separation and quantitation of glucuronic acid and iduronic acid. This method is quite simple, and glucuronic acid and iduronic acid can be separated within 50 min. This method was applied to the analyse
A 'gas chromatographic method for the quantitative analysis of iduronic acid and glucuronic acid in sulfated glycosaminoglycans (acid mucopolysaccharides, AMPS) of the type of dermatan sulfate has been developed. Methanolysis and deamination-methanolysis were used for the depolymerization of AMPS. B
Small proteoglycans (PGs), extracted from human keloid scar tissue with 4M guanidinium chloride and fractionated by DEAE-cellulose chromatography, were separated by ethanol precipitation into one L-iduronic acid-rich and one D-glucuronic acid-rich fraction. The size of the L-iduronic acid-rich PG wa