155404-25-4Relevant academic research and scientific papers
Synthesis of 5-thialdopentopyranoside via dithioacetal rearrangement and glycosidation to give pseudodisaccharides
Lepine, Carole,Roy, Caroline,Delorme, Daniel
, p. 1843 - 1846 (1994)
Rearrangement of acetylated 5-O-p-toluenesulfonyl-L-arabinose dibenzyl dithioacetal 10 gave benzyl 1,5-dithio-L-arabinopyranoside 6 which upon anomeric bromination followed by glycosidation led to pseudodisaccharide 20 containing a sulfur atom in the ring of the non-reducing unit. Similarly, benzyl 1,5-dithio-D-lyxopyranoside 17 was obtained from 5-O-p-toluenesulfonyl-D-lyxose dibenzyl dithioacetal 16.
