Show simple item record Best, Daniel Jenkinson, Sarah F. Thompson, Amber L. Watkin, David J. Wilson, Francis X. Nash, Robert J. Fleet, George W. J. 2012-10-23T10:05:30Z 2012-10-23T10:05:30Z 2009-09-09
dc.identifier.citation Best , D , Jenkinson , S F , Thompson , A L , Watkin , D J , Wilson , F X , Nash , R J & Fleet , G W J 2009 , ' (2S,3R,4R,5R)-3,4-Dihydroxy-5-hydroxymethyl)pyrrolidine-2-carboxylic acid [(2S,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)proline] ' Acta Crystallographics Section E-Structure Reports Online , vol 65 , no. 10 , pp. o2418-o2419 . , 10.1107/S1600536809035636 en
dc.identifier.issn 1600-5368
dc.identifier.other PURE: 176872
dc.identifier.other dspace: 2160/7891
dc.description Best, D., Jenkinson, S. F., Thompson, A. L., Watkin, D. J., Wilson, F. X., Nash, R. J., Fleet, G. W. J. (2009). (2S,3R,4R,5R)-3,4-Dihydroxy-5-hydroxymethyl)pyrrolidine-2-carboxylic acid [(2S,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)proline]. Acta Crystallographics Section E-Structure Reports Online, 65, O2418. en
dc.description.abstract The crystal structure of the title compound, C(6)H(11)NO(5), establishes the relative configuration at the four stereogenic centres; the absolute configuration is determined by the use of D-glucuronolactone as the starting material for the synthesis. Molecules are linked by intermolecular O-H center dot center dot center dot O and N-H center dot center dot center dot O hydrogen bonds into a three-dimensional network, with each molecule acting as a donor and acceptor for five hydrogen bonds. en
dc.language.iso eng
dc.relation.ispartof Acta Crystallographics Section E-Structure Reports Online en
dc.title (2S,3R,4R,5R)-3,4-Dihydroxy-5-hydroxymethyl)pyrrolidine-2-carboxylic acid [(2S,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)proline] en
dc.type Text en
dc.type.publicationtype Article (Journal) en
dc.contributor.institution Institute of Biological, Environmental and Rural Sciences en
dc.description.status Peer reviewed en

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