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Reliable Synthesis of Various Nucleoside Diphosphate Glycopyranoses
Authors:Saskia Wolf Dipl‐Chem  Tanja Zismann Dipl‐Chem  Nathalie Lunau Dipl‐Chem  Chris Meier Prof?Dr
Institution:Organic Chemistry, Department of Chemistry, Faculty of Science, University of Hamburg, Martin‐Luther‐King‐Platz 6, 20146 Hamburg (Germany), Fax: (+49)?40‐42838‐5592
Abstract:A reliable and high yielding synthetic pathway for the synthesis of the biologically highly important class of nucleoside diphosphate sugars (NDP‐sugars) was developed by using various cycloSal‐nucleotides 1 and 9 as active ester building blocks. The reaction with anomerically pure pyranosyl‐1‐phosphates 2 led to the target NDP‐sugars 20 – 45 in a nucleophilic displacement reaction, which cleaves the cycloSal moiety in anomerically pure forms. As nucleosides cytidine, uridine, thymidine, adenosine, 2′‐deoxy‐guanosine and 2′,3′‐dideoxy‐2′,3′‐didehydrothymidine were used while the phosphates of D ‐glucose, D ‐galactose, D ‐mannose, D ‐NAc‐glucosamine, D ‐NAc‐galactosamine, D ‐fucose, L ‐fucose as well as 6‐deoxy‐D ‐gulose were introduced.
Keywords:glycophosphotransferases  glycosylation  nucleotide sugars  sugar conjugates
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