
%0 Journal Article
%A Conway, RJ 
%A Nagel, JP 
%A Stick, RV 
%A Tilbrook, DMG 
%T Further Aspects of the Reduction of Dithiocarbonates with Tributyltin Hydride and Deuteride
%J Australian Journal of Chemistry
%D 1985/06/01
%V 38
%N 6
%P 939-945
%K 
%R https://doi.org/10.1071/CH9850939
%U https://www.publish.csiro.au/paper/CH9850939 
%X 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. 
