Skip to main content
Article
Structure and conformation of tri-O-acetyl-D-glucal dimer in solid state and in solution
Mendeleev Communications
  • Andreas H. Franz, University of the Pacific
  • Viktor V. Zhdankin, The University of Minnesota, Duluth
  • Vyacheslav V. Samoshin, University of the Pacific
  • Michael J. Minch, University of the Pacific
  • Victor G. Young, Jr., X-Ray Crystallographic Laboratory
  • Paul H. Gross, University of the Pacific
Document Type
Article
Department
Chemistry
DOI
10.1070/MC1999v009n02ABEH001061
Publication Date
1-1-1999
Disciplines
Abstract
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.
Citation Information
Andreas H. Franz, Viktor V. Zhdankin, Vyacheslav V. Samoshin, Michael J. Minch, et al.. "Structure and conformation of tri-O-acetyl-D-glucal dimer in solid state and in solution" Mendeleev Communications Vol. 9 Iss. 2 (1999) p. 45 - 47 ISSN: 0959-9436
Available at: http://works.bepress.com/andreas-franz/59/