Synthesis of Three Hetero Disaccharides, 4-O-β-Glucopyranosyl-6-deoxy-D-glucose, 4-O-β-D-Glucopyranosyl-D-mannosamine, and 4-O-β-D-Glucopyranosyl-D-mannose, and Confirmation of Their Structures by C-13 NMR and MS
✍ Scribed by M.A. Tariq; K. Hayashi
- Book ID
- 115577245
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 365 KB
- Volume
- 214
- Category
- Article
- ISSN
- 0006-291X
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📜 SIMILAR VOLUMES
The disaccharides 4-O-/3-D-glucopyranosyl-D-glucosamine (GIc-GIcN) and 4-O-fl-D-glucopyranosyl-2-deoxy-o-glucose (Glc-2-deoxy-Glc) were synthesized from equimolar amounts of D-glucosamine and a-D-glucose-l-phosphate (G-l-P), and 2-deoxy-o-glucose and at-D-glucose-Iphosphate (G-l-P) respectively, in
Recent years have seen a remarkable surge of interest in the study of U-Lfucosyltransferases. Of these L-fucosyltransferases, the enzyme (143)~a+fucosyltransferase has attracted a great deal of clinical interest as a potential tumor marker. This enzyme catalyzes the transfer of an L-fucosyl group f
## Crystals of the tetrasaccharide, (2,3,4,6-tetra-0acetyl-fi-D-ghxopyranosyl~-(1 + 3)-[2,3,4,6-tetra-O-acetyI+LD-gIucopyranosyI-(1 --t 6)]-(2,4-di-0-acetyl-g\_D-glucopyranosyl)-1 --) 3)-1,2,4,6-tetrad-acetyl$?-n-ghicopyranose, belong to tge monoclinic system, space group P2,, with a = 12.709(4),