## 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),
An. n.m.r. study of the 1,3,4,6- and 1,2,3,6-tetra-acetates of β-d-allopyranose and the X-ray and structure of the former
✍ Scribed by Elizabeth Lee; Patricia Browne; Patrick McArdle; Desmond Cunningham
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 296 KB
- Volume
- 224
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
✦ Synopsis
Reaction of j?-D-allopyranose with acetic anhydride (7.5 mol)-sodium acetate at room temperature and chromatography of the products gave the known' crystalline /Spyranose penta-acetate (5, 36%), together with the hitherto unknown /Spyranose 1,3,4,6 (1, 21%) and 1,2,3,6-tetra-acetate
(2, 12%).
📜 SIMILAR VOLUMES
Both 'H-and 13C-n.m.r. spectroscopy have been employed in structural studies of the 4,6-O-benzylidene-D-aldohexopyranosides and derivatives, including some deoxy sugars . I4 We now report i3C-n.m.r. data (Table I) for the 4,6-O-benzylidene derivatives of methyl 2-deoxy-( 2) 2-deoxy-3-O-methyl-(3),