
TY  - JOUR
A1  - Conway, RJ 
A1  - Nagel, JP 
A1  - Stick, RV 
A1  - Tilbrook, DMG 
T1  - Further Aspects of the Reduction of Dithiocarbonates with Tributyltin Hydride and Deuteride
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1985
VL  - 38
IS  - 6
SP  - 939
EP  - 945
KW  - 
UR  - https://doi.org/10.1071/CH9850939 
N2  - The reduction of 1,2:5,6-di-O-isopropylidene-3-O-(methylthio) thiocarbonyl-&#946;-D-idose ,- talose, and -(3-2H) talose with tributyltin hydride and deuteride leads to the deoxy sugar and some deuterium-containing deoxy sugars. A modification of the normal procedure allows for reduction with tributyltin hydride generated in situ. As well, the reduction of some dithiocarbonates derived from glycosides of N-acetyl-D- glucosamine allows access to a variety of dideoxy and trideoxy sugars. 
ER  -

