
%0 Journal Article
%A Stick, Robert V. 
%A Tilbrook, D. Matthew G. 
%A Williams, Spencer J. 
%T 1,6-Epithio- and 1,6-Episeleno-<emph type="2">&#946;</emph>-D-glucopyranose: Useful Adjuncts in the Synthesis of 6-Deoxy-<emph type="2">&#946;</emph>-D-glucopyranosides
%J Australian Journal of Chemistry
%D 1999/08/19
%V 52
%N 7
%P 685-694
%K 
%R https://doi.org/10.1071/CH99009
%U https://www.publish.csiro.au/paper/CH99009 
%X Derivatives of 1,6-dideoxy-1,6-epithio- and 1,6-dideoxy-1,6-episeleno-&#946;-D-glucopyranose have been shown to be effective glycosyl donors toward carbohydrate alcohols under the agency of N- iodosuccinimide/trifluoromethanesulfonic acid. Reduction of the intermediate disulfides and diselenides affords 6-deoxy-&#946;-D-glucopyranosides. The synthesis of a range of such 6&#8242;-deoxy disaccharide derivatives is reported. 
