Further justification for the <i>exo</i>-anomeric effect. Conformational analysis based on nuclear magnetic resonance spectroscopy of oligosaccharides

Henning Thøgersen(University of Alberta), Raymond U. Lemieux(University of Alberta), Klaus Bock(University of Alberta), Bernd Meyer(University of Alberta)
Canadian Journal of Chemistry
January 1, 1982
Cited by 341Open Access
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Abstract

Hard-sphere (HS) calculations predict three conformers for the branched B human blood group antigenic determinant (α LFuc(1 → 2)[α DGal(1 → 3)]βDGal) and two conformers for the linear tetrasaccharide (αLRha(1 → 2)αLRha(1 → 3)αLRha(1 → 3)βDGlcNAc), which constitutes a part of the repeating unit of the Shigellaflexneri O-antigen, which differ in conformational energy by less than 0.7 and 0.2 kcal/mol, respectively. However, a detailed 1 H nmr study of specific interunit deshielding effects, quantitative treatment of spin-lattice relaxation times, and nuclear Overhauser enhancements requires that only one of the conformers thus predicted be, in fact, conformationally preferred in solution. These conformers are those predicted by hard-sphere exo-anomeric (HSEA) calculations.


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