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Peracetylated laminaribiose: preparation by specific degradation of curdlan and its chemical conversion into N-acetylhyalobiuronic acid.
Wang LX, Sakairi N, Kuzuhara H. Wang LX, et al. Carbohydr Res. 1991 Oct 14;219:133-48. doi: 10.1016/0008-6215(91)89048-k. Carbohydr Res. 1991. PMID: 1804530
The usefulness of these peracetates 2a and 2b as starting materials for organic synthesis was shown by converting 2b into N-acetylhyalobiuronic acid (23), the disaccharide repeating unit of hyaluronic acid. ...
The usefulness of these peracetates 2a and 2b as starting materials for organic synthesis was shown by converting 2b into N-acetyl …
Compositional analysis of hyaluronan, chondroitin sulfate and dermatan sulfate: HPLC of disaccharides produced from the glycosaminoglycans by solvolysis.
Qiu G, Toyoda H, Toida T, Koshiishi I, Imanari T. Qiu G, et al. Chem Pharm Bull (Tokyo). 1996 May;44(5):1017-20. doi: 10.1248/cpb.44.1017. Chem Pharm Bull (Tokyo). 1996. PMID: 8689716
An ion-exchange high-performance liquid chromatography procedure was developed for analysis of mixtures of N-acetyldermosine, N-acetylchondrosine and N-acetylhyalobiuronic acid produced quantitatively by heating dermatan sulfate, chondroitin sulfate and hyalu …
An ion-exchange high-performance liquid chromatography procedure was developed for analysis of mixtures of N-acetyldermosine, N-acetylchondr …
Chemical change involved in the oxidative reductive depolymerization of hyaluronic acid.
Uchiyama H, Dobashi Y, Ohkouchi K, Nagasawa K. Uchiyama H, et al. J Biol Chem. 1990 May 15;265(14):7753-9. J Biol Chem. 1990. PMID: 2335504 Free article.
The following structures derived from the nonreducing ends were identified: L-threo-tetro-dialdosyl-(1----3)GlcNAc (a tentative structure, 8%), N-acetylhyalobiuronic acid (20%), and N-acetyl-D-glucosamine (45%). ...
The following structures derived from the nonreducing ends were identified: L-threo-tetro-dialdosyl-(1----3)GlcNAc (a tentative structure, 8 …