
TY  - JOUR
A1  - Roush, W. R. 
A1  - James, R. A. 
T1  - 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
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 2002
VL  - 55
IS  - 2
SP  - 141
EP  - 146
KW  - 
UR  - https://doi.org/10.1071/CH01199 
N2  - 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). 
ER  -

