Collect. Czech. Chem. Commun.
1980, 45, 2779-2783
https://doi.org/10.1135/cccc19802779
13C NMR study of tetrosides and their derivatives
Jiří Urbana, Miroslav Marekb, Jiří Jarýb and Petr Sedmeraa
a Institute of Microbiology, Czechoslovak Academy of Sciences, 142 20 Prague 4
b Laboratory of Monosaccharides, Prague Institute of Chemical Technology, 166 28 Prague 6
Abstract
13C NMR spectra of 23 tetrose derivatives were assigned. The C(1) resonates below 103 ppm with compounds having cis-arranged substituents at C(1) and C(2) and above 106 ppm with compounds having trans-arrangement. The carbon-13 chemical shifts are mainly influenced by the 1,2-interaction. The magnitudes of direct coupling constants 1J(C(1), H) cannot be used for the determination of the anomeric configuration.
