The solid-state conformation of the title compound, C 14 H 20 N 2 O 3 Á0.33H 2 O, a potent hexosaminidase inhibitor, prepared from d-lyxonolactone, has been established by X-ray crystallography. The asymmetric unit contains three molecules, which have very similar conformations, together with a mole
2-Acetamido-N-benzyl-1,4-imino-1,2,4-trideoxy-l-ribitol
✍ Scribed by Harding, Christopher C. ;Watkin, David J. ;Rountree, J. S. Shane ;Butters, Terry D. ;Wormald, Mark R. ;Dwek, Raymond A. ;Fleet, George W. J.
- Book ID
- 104483700
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 276 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
No coin nor oath required. For personal study only.
✦ Synopsis
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.
📜 SIMILAR VOLUMES
The N-containing ring of the tetrahydroisoquinolinium ion of the title compound, C~19~H~24~NO~3~ ^+^·SCN^−^, has a half-chair conformation. There is a network of hydrogen bonds between the phenolic groups and thiocyanate anions.
Qivhm of Bio&emisby and Metahrdi~~~, lnrtihde of Child H~ltb (U oiwmily of