Abstract
X-ray crystallography defines the relative configuration at the three-stereogenic centres in the title compound N-benzyl-l-XYLNAc, C 14H20N2O3. The five-membered pyrrolidine ring adopts an envelope conformation with the N atom lying out of the plane of the other four atoms. In the crystal structure, intermolecular O - H⋯O, N - H⋯O and O - H⋯N hydrogen bonds link the molecules into chains along [100]. The carbonyl group O atom acts as an acceptor for a bifurcated hydrogen bond. The absolute configuration is determined by the use of l-glucuronolactone as the starting material for the synthesis. © 2010.
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CITATION STYLE
Jenkinson, S. F., Crabtree, E. V., Glawar, A. F. G., Butters, T. D., Fleet, G. W. J., & Watkin, D. J. (2010). 2-Acetamido-N-benzyl-1,4-imino-1,2,4-trideoxy-L-xylitol (N-benzyl-L-XYLNAc). Acta Crystallographica Section E: Structure Reports Online, 66(5). https://doi.org/10.1107/S1600536810014145
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