Open Access2‐Acetamido‐ N ‐benzyl‐1,4‐imino‐1,2,4‐trideoxy‐ l ‐ribitol
Author(s) -
Harding Christopher C.,
Watkin David J.,
Rountree J. S. Shane,
Butters Terry D.,
Wormald Mark R.,
Dwek Raymond A.,
Fleet George W. J.
Publication year - 2005
Publication title -
acta crystallographica section e
Language(s) - English
Resource type - Journals
ISSN - 1600-5368
DOI - 10.1107/s1600536805006926
Subject(s) - ribitol , chemistry , d glucopyranose , stereochemistry , organic chemistry , enzyme
The relative configuration of the stereocentres in a potential hexosaminidase inhibitor, C 14 H 20 N 2 O 3 , prepared from d ‐lyxonolactone, has been established using X‐ray crystallographic techniques.