
TY  - JOUR
A1  - Copeland, C 
A1  - Mcadam, DP 
A1  - Stick, RV 
T1  - The reaction of N-dichloromethylene-N,N-dialkylammonium chlorides with free sugars: an efficient synthesis of glycosyl chlorides
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1983
VL  - 36
IS  - 6
SP  - 1239
EP  - 1247
KW  - 
UR  - https://doi.org/10.1071/CH9831239 
N2  - 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. 
ER  -

