Conclusions and Future Direction
In this poster we presented results from a series of theoretical studies on the
dependence of the anomeric carbon 13C chemical shift with the glycosidic bond dihedral angles for a representative series of disaccharide and glycopeptide models. Our results are in agreement with experimental observations and earlier theoretical calculat
The mathematical functions derived from the 13C chemical shift surfaces could
be in principle used as an aid in conformational studies, particularly for large polysaccharides, glycoproteins, and glycolipids for which the measurement of NOEs and J-couplings can prove experimentally unfeasible. However, exhaustive comparisons between
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