Literature DB >> 19057077

The absolute configuration of 1-epialexine hemihydrate.

Amber L Thompson1, David J Watkin, Zoltan A Gal, Laurence Jones, Jackie Hollinshead, Sarah F Jenkinson, George W J Fleet, Robert J Nash.   

Abstract

The absolute and relative configurations of 1-epialexine are established by X-ray crystallographic analysis, giving (1S,2R,3R,7S,7aS)-1,2,7-trihydroxy-3-(hydroxymethyl)pyrrolizidine. The compound crystallizes as the hemihydrate C(8)H(15)NO(4) x 0.5H(2)O, with hydrogen bonds holding the water molecule in a hydrophilic pocket between epialexine bilayers. In addition, a comparison was made between results obtained from examination of the Bijvoet pairs from data sets collected using molybdenum and copper radiation.

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Year:  2008        PMID: 19057077     DOI: 10.1107/S0108270108037086

Source DB:  PubMed          Journal:  Acta Crystallogr C        ISSN: 0108-2701            Impact factor:   1.172


  2 in total

1.  (S)-(Z)-Methyl 2-[2,3-bis-(benzyl-oxy-carbon-yl)guanidino]-4-methyl-penta-no-ate.

Authors:  Chris F Fronczek; Hyunjoo Kil; Mark L McLaughlin; Frank R Fronczek
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-12-04

2.  (2S,3R,4R,5R)-3,4-Dihydr-oxy-5-(hydroxy-meth-yl)pyrrolidine-2-carboxylic acid [(2S,3R,4R,5R)-3,4-dihydr-oxy-5-(hydroxy-meth-yl)proline].

Authors:  Daniel Best; Sarah F Jenkinson; Amber L Thompson; David J Watkin; Francis X Wilson; Robert J Nash; George W J Fleet
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-09-09
  2 in total

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