59532-35-3

Upstream product

• 17241-04-2 bis(p-tolylthio)methane 
• 1517-82-4 (-)-menthyl p-toluenesulfinate 
• 10486-08-5 sodium p-thiocresolate 
• 31350-96-6 (S)-1-(bromomethylsulfinyl)-4-methylbenzene 
• 34125-84-3 chloromethyl p-tolyl sulfide 
• 1519-39-7 (R)-methyl p-tolyl sulfoxide 

Downstream Products

• 67252-11-3 4-Methylphenyl 4-methylphenylthio-(3-oxocyclopentyl)-methyl sulfoxide 
• 83408-17-7 1-Phenyl-2-((S)-toluene-4-sulfinyl)-2-p-tolylsulfanyl-ethanone 
• 77852-93-8 7-{5-Hydroxy-5-[((S)-toluene-4-sulfinyl)-p-tolylsulfanyl-methyl]-cyclopent-1-enyl}-heptanoic acid methyl ester 
• 77852-90-5 7-{(1S,5R)-2-Oxo-5-[((S)-toluene-4-sulfinyl)-p-tolylsulfanyl-methyl]-cyclopentyl}-heptanoic acid methyl ester 
• 78517-52-9 3-Phenyl-1-((S)-toluene-4-sulfinyl)-1-p-tolylsulfanyl-propan-2-ol 
• 78549-08-3 (1S,2S,3S)-1-phenyl-2-p-tolylthio-2-p-tolylsulphinylethanol 
• 78549-07-2 (1R,2R,3S)-1-phenyl-2-p-tolylthio-2-p-tolylsuphinylethanol 
• 78549-06-1 (1R,2S,3S)-1-phenyl-2-p-tolylthio-2-p-tolylsulphinylethanol 
• 89921-65-3 (1S,2R,3S)-1-phenyl-2-p-tolylthio-2-p-tolylsulphinylethanol 
• 78517-51-8 (E)-(+)-(S)-1-p-tolylsulphinyl-1-p-tolylthio-2-phenylethylene 
• 78549-06-1 1-Phenyl-2-((S)-toluene-4-sulfinyl)-2-p-tolylsulfanyl-ethanol 
• 86448-57-9 (S)-1-Phenyl-2-((S)-toluene-4-sulfinyl)-2-p-tolylsulfanyl-ethanone 
• 86448-58-0 (R)-1-Phenyl-2-((S)-toluene-4-sulfinyl)-2-p-tolylsulfanyl-ethanone 
• 119496-34-3 5-[1-(tert-Butyl-dimethyl-silanyloxy)-2-((S)-toluene-4-sulfinyl)-2-p-tolylsulfanyl-ethyl]-3-phenyl-4,5-dihydro-isoxazole 

Relevant academic research and scientific papers

AN IMPROVED PROCEDURE FOR EFFICIENT GENERATION OF METHYL(OR p-TOLYL)THIOMETHYL GRIGNARD REAGENT AND ITS USE IN ORGANIC SYNTHESES

The optimal condition for transformation of a chloromethyl sulfide into the corresponding Grignard reagent (2) in a high yield are established and 2 is shown to react with various functional groups such as an alkyl halide, an aldehyde, and a sulfinic este

Stereoselective Enzyme-catalysed Oxidation-Reduction Reactions of Thioacetals-Thioacetal Sulphoxides by Fungy

Enzymes present in the fungus Mortierella isabellina catalyse the transfer of an oxygen atom to the cyclic thioacetal 1,3-dithian and from 1,3-dithian 1-oxide, 1,3,5-trithian 1-oxide, and cis-1,3-dithian 1,3-dioxide.The oxidation of 1,3-dithian and the acyclic thioacetal bis-(p-tolylthio)methane to form the corresponding monosulphoxides occurred in the presence of growing cultures of Aspergillus foetidus and a Helminthosporium species.The degree and the preferred direction of stereoselectivity occurring during the asymmetric oxidation and reduction steps was deduced from the enantiomeric excess (e.e.) and absolute stereochemistry of the isolated 1,3-dithian 1-oxide and p-tolylthio-(p-tolylsulphinyl)metane.

A TWO-PHASE REACTION CATALYZED BY A PROTEIN - ASYMETRIC OXIDATION OF FORMALDEHYDE DITHIOACETALS WITH AQUEOUS SODIUM METAPERIODATE

We examined whether a protein could catalyze two-phase oxidation of formaldehyde dithioacetals with aqueous sodium metaperiodate and bovine serum albumin was found to be effective and give the corresponding S-oxides in optically active forms.