Structure and conformation of tri-O-acetyl-D-glucal dimer in solid state and in solution

Authors

Andreas H. Franz, University of the PacificFollow
Viktor V. Zhdankin, The University of Minnesota, Duluth
Vyacheslav V. Samoshin, University of the PacificFollow
Michael J. Minch, University of the PacificFollow
Victor G. Young Jr., X-Ray Crystallographic Laboratory
Paul H. Gross, University of the PacificFollow

Document Type

Article

Publication Title

Mendeleev Communications

Department

Chemistry

ISSN

0959-9436

Volume

9

Issue

2

DOI

10.1070/MC1999v009n02ABEH001061

First Page

45

Last Page

47

Publication Date

1-1-1999

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.

Recommended Citation

Franz, A. H., Zhdankin, V. V., Samoshin, V. V., Minch, M. J., Young, V. G., & Gross, P. H. (1999). Structure and conformation of tri-O-acetyl-D-glucal dimer in solid state and in solution. Mendeleev Communications, 9(2), 45–47. DOI: 10.1070/MC1999v009n02ABEH001061
https://scholarlycommons.pacific.edu/cop-facarticles/122