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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

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✦ 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.


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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

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