"Structure and conformation of tri-O-acetyl-D-glucal dimer in solid state and in solution" by Andreas H. Franz

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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

Link

Document Type

Article

Department

Chemistry

DOI

10.1070/MC1999v009n02ABEH001061

Publication Date

1-1-1999

Disciplines

Chemistry

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/