Structure and conformation of tri-O-acetyl-D-glucal dimer in solid state and in solution
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.
Franz, A. H.,
Zhdankin, V. V.,
Samoshin, V. V.,
Minch, M. J.,
Young, V. G.,
Gross, P. H.
Structure and conformation of tri-O-acetyl-D-glucal dimer in solid state and in solution.
Mendeleev Communications, 9(2), 45–47.