
%0 Journal Article
%A Copeland, C 
%A Stick, RV 
%T The reaction of N-dichloromethylene-N,N-dimethylammonium chloride (Viehe's salt) with methyl 4,6-O-benzylidene-&#945;-D-glucoside. An alternative synthesis of methyl 4,6-O-benzylidene-&#945;-D-alloside
%J Australian Journal of Chemistry
%D 1982/05/01
%V 35
%N 5
%P 1031-1036
%K 
%R https://doi.org/10.1071/CH9821031
%U https://www.publish.csiro.au/paper/CH9821031 
%X The reaction of methyl 4,6-O-benzylidene-&#945;-D-glucoside with N-dichloromethylene-N,N-dimethyl-ammonium chloride (Viehe's salt) in the presence of a base gives a mixture of carbamates (with triethylamine) or the 2,3-carbonate mainly (with pyridine). The treatment of this carbonate with various primary and secondary amines, again to give mixtures of carbamates, and an efficient synthesis of methyl 4,6-O-benzylidene-&#945;-D-alloside from one of the gluco carbamates, are reported. 
