X-Ray crystallography and 1H NMR spectroscopy indicate that the conformations of both rings A and B and the relative orientation of the rings in the C-linked disaccharide 1,3,4,6-tetra-O-acetyl-2-C-(4,6-di-O-acetyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranosyl)-2-deoxy-β-D-glucopyranose in solution are virtually identical to the crystalline structure.
A. H. Franz, V. V. Zhdankin, V. V. Samoshin, M. J. Minch, V. G. Young and P. H. Gross, Mendeleev Commun., 1999, 9, 45 DOI: 10.1070/MC1999v009n02ABEH001061
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