118149-35-2

Upstream product

• 118149-34-1 (S)-1-((3aS,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-2-phenylsulfanyl-ethanol 
• 22529-61-9 (1R)-1-((3aR,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro(2,3-d)(1,3)dioxol-5-yl)ethane-1,2-diol 
• 23313-03-3 (R)-2-[(3aR,5R,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]-2-hydroxyethyl 4-methylbenzenesulfonate 
• 118149-34-1 (S)-1-((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-2-phenylsulfanyl-ethanol 

Relevant academic research and scientific papers

TELLURIUM DIOXIDE CATALYZED SELECTIVE OXIDATION OF SULFIDES TO SULFOXIDES WITH HYDROGEN PEROXIDE

TeO2-H2O2 system was found to be an efficient selective reagent for the oxidation of sulfides to sulfoxides in the presence of other common functional groups.Over-oxidation of sulfoxides to sulfones was not observed.

SYNTHESIS OF HIGHER-CARBON SUGARS: PREPARATION AND REACTION OF β-HYDROXYSULFONYL SUGARS

β-Hydroxysulfonyl sugars 4 and 5 were prepared by addition of phenylsulfonylmethide to a dialdose 3 and by oxidation of a sulfide sugar 8 with H2O2-H2SeO3.The dianion of 4 was stable at low temperature and reacted with carbon electrophiles to provide vari