A nitro sugar derivative route to 2-thioepisophorose and 2-thiosophorose and their remarkable facile epimerization

The addition of 1-thio-d-glucose sodium salt to per-O-acetylated 1,2-dideoxy-1-nitro-d-arabino-hex-1-enitol, readily available from d-arabinose, afforded the corresponding 2-S-glycosylated 1-deoxy-1-nitro-d-mannitol and -d-glucitol peracetates. These, after deacetylation, were transformed by the Nef reaction to 2-thioepisophorose and 2-thiosophorose, respectively. The 2-thiodisaccharides easily epimerize in aqueous sodium bicarbonate at ambient temperature to a 1:4 equilibrium mixture. The predominant 2-thiosophorose was obtained crystalline. A 1H NMR study of the epimerization in deuterium oxide showed that the reaction involves an H-2 proton exchange mechanism.