
%0 Journal Article
%A Roush, W. R. 
%A James, R. A. 
%T Towards the Synthesis of Aureolic Acid Analogue Conjugates: Synthesis and Glycosidation Reactions of 3-<emph type="2">O</emph>-Acetyl-4-azido-2,4,6-trideoxy-<font size="-2">L</font>-glucopyranose Derivatives
%J Australian Journal of Chemistry
%D 2002/06/04
%V 55
%N 2
%P 141-146
%K 
%R https://doi.org/10.1071/CH01199
%U https://www.publish.csiro.au/paper/CH01199 
%X A stereoselective synthesis of 3-O-acetyl-4-azido-glucopyranose (6) is described. The derived anomeric acetate (13), and especially the thioglycoside (14), are demonstrated to be good donors for synthesis of &#945;-glycosides of (6). Donor (14) was used in the synthesis of trisaccharide (21), which is targeted for use in the synthesis of the aureolic acid trisaccharide conjugate analogue (5). 
