37605-77-9

Upstream product

• 28118-53-8 1,3-bis(phenylthio)propane 
• 30134-12-4 phenyl 3-phenylpropyl sulfide 

Downstream Products

• 94404-34-9 C₁₅H₁₅FS 
• 150312-10-0 C₁₅H₁₄Cl₂S 
• 214207-19-9 4-phenyl-1-(2-phenylethyl)-1-phenylsulfinyl-2-butanol 
• 303143-99-9 1-(3-phenyl-1-phenylsulfinylpropyl)cyclohexanol 
• 94404-40-7 C₁₅H₁₅FOS 
• 155725-28-3 1-(1-naphthyl)-4-phenyl-2-(phenylsulfinyl)-1-butanone 
• 155725-27-2 1-(2-naphthyl)-4-phenyl-2-(phenylsulfinyl)-1-butanone 
• 155725-31-8 1-(4-phenylbut-1-yn-1-yl)naphthalene 
• 95607-27-5 1,4-diphenyl-2-(phenylsulfinyl)-1-butanone 
• 40164-53-2 1,4-diphenyl-1-butyne 
• 214207-29-1 3-mesyloxy-1,6-diphenyl-4-phenylsulfonylhexane 
• 303144-02-7 1-(1-acetoxycyclohexyl)-3-phenyl-1-phenylsulfinylpropane 
• 85185-32-6 (E)-1-(3,4-methylenedioxyphenyl)-4-phenyl-1-butene 
• 52376-48-4 1-cyclohexylidene-3-phenylpropane 

Relevant academic research and scientific papers

Rapid dehydrosulfenylation of sulfoxides under microwave irradiation

Pyrolytic β-elimination of sulfoxides has been promoted by microwave irradiation. The reaction is very fast and yields are almost quantitative.

Facile oxidation of sulfides to sulfoxides using sodium hypochlorite and oxoammonium salt as a catalyst: Chemo- and diastereoselective transformation of bis(phenylthio)alkanes into sulfoxides

A facile and selective method for the title transformation is described. The two-phase oxidation of disulfides with one or two equivalents of sodium hypochlorite mediated by TEMPO and cocatalyzed by potassium bromide and PTC leads to the corresponding mon