
TY  - JOUR
A1  - Dalton, LK 
T1  - The preparation of Thiazolidine-2-thiones from N-alkylglucosylamines
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1966
VL  - 19
IS  - 3
SP  - 445
EP  - 450
KW  - 
UR  - https://doi.org/10.1071/CH9660445 
N2  - N-Alkylglucosylamines and carbon disulphide react to give 3-alkyl-5-hydroxy- 5-(D-arabino-tetrahydroxybutyl)thiazolidine-2-thiones (I), which dehydrate to the corresponding &#916;4-thiazolines, isolated only as tetraacetates. A thiazolidine-2-thione forms also from the action of carbon disulphide on 1-N-methylamino-1-deoxy-D-fructose.   l-Bromo-l-deoxy-2,3:4,5-di-O-isopropylidene-D-fructose is obtained by the action of dibromotriphenoxyphosphorane on 2,3:4,5-di-O-isopropylidene-D-fructose. 
ER  -

