Acta Crystallographica Section E (Aug 2009)

2,6-Dideoxy-2,6-imino-l-glycero-d-ido-heptitol

  • Sarah F. Jenkinson,
  • K. Victoria Booth,
  • Scott Newberry,
  • George W. J. Fleet,
  • Ken Izumori,
  • Kenji Morimoto,
  • Robert J. Nash,
  • Laurence Jones,
  • David J. Watkin,
  • Amber L. Thompson

DOI
https://doi.org/10.1107/S1600536809025045
Journal volume & issue
Vol. 65, no. 8
pp. o1755 – o1756

Abstract

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The title molecule, C7H15NO5, the major product from selective enzymatic oxidation followed by hydrogenolysis of the corresponding azidoheptitol, was found by X-ray crystallography to exisit in a chair conformation with three axial hydroxyl groups. One of the hydroxymethyl groups is disordered over two sets of sites in a 0.590 (3):0.410 (3) ratio. In the crystal, O—H...O, O—H...(O,O), O—H...N and N—H...O hydrogen bonding occurs.