z-logo
Premium
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
Author(s) -
Hirano Shigehiro
Publication year - 1970
Publication title -
organic magnetic resonance
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0030-4921
DOI - 10.1002/mrc.1270020608
Subject(s) - moiety , chemistry , stereochemistry , nuclear magnetic resonance spectroscopy , polysaccharide , digestion (alchemy) , hyaluronic acid , biochemistry , chromatography , biology , genetics
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.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom