✦ LIBER ✦
NMR study of 4-deoxy-α-L-threo-4-enohexopyranosyluronic acid (1 → 3)2-acetamido-2-deoxy-D-hexoses produced in the enzymic digestion of hyaluronate, chondroitin and chondroitin sulfates
✍ Scribed by Shigehiro Hirano
- Publisher
- John Wiley and Sons
- Year
- 1970
- Tongue
- English
- Weight
- 201 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The conformation of 4‐deoxy‐α‐L‐threo‐4‐enohexopyranosyluronic acid (1 → 3)2‐acetamido‐2‐deoxy‐d‐hexoses was analyzed by NMR spectroscopy. The half‐chair (H~1~^2^) conformation was found in the unsaturated uronide moiety and the chair (Cl) conformation in the hexosamine moiety.