
%0 Journal Article
%A Copeland, C 
%A Mcadam, DP 
%A Stick, RV 
%T The reaction of N-dichloromethylene-N,N-dialkylammonium chlorides with free sugars: an efficient synthesis of glycosyl chlorides
%J Australian Journal of Chemistry
%D 1983/06/01
%V 36
%N 6
%P 1239-1247
%K 
%R https://doi.org/10.1071/CH9831239
%U https://www.publish.csiro.au/paper/CH9831239 
%X The treatment of aldose derivatives that are protected at all but the anomeric hydroxy groups with N-dichloromethylene-N,N-dialkylammonium chlorides (alkyl = Me, Et) provides an improved method of preparing the corresponding glycosyl chlorides. Analogous derivatives containing anunprotected C1-C2 diol give 2-O-(N,N-dialkylcarbamoyl)glycosyl chlorides. 
