
TY  - JOUR
A1  - McLaren, JM 
A1  - Stick, RV 
A1  - Webb, S 
T1  - A synthesis of 2,2,2-Trichloroethyl 2-Acetamido-3,6-di-O-acetyl-2-deoxy-&#946;-D-glucopyranoside
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1977
VL  - 30
IS  - 12
SP  - 2689
EP  - 2693
KW  - 
UR  - https://doi.org/10.1071/CH9772689 
N2  - The conversion of 2-acetamido-2-deoxy-D-glucose into 2-acetamido-3,4,6- tri-O-acetyl-2-deoxy-&#945;-D-glucosyl chloride has been reinvestigated and the chloride transformed, with some modification of the literature method, into 2,2,2-trichloroethyl 2-acetamido-4,6-O-benzylidene-2- deoxy-&#946;-D-glucoside. This compound has been converted into the title compound by the sequence acetylation, acid hydrolysis and selective acetylation. An efficient synthesis of benzyl 2,3-di-O-acetyl-&#946;-D- galacto-pyranosideis reported and its unsuccessful selective acetylation contrasted with the above. 
ER  -

