69979-69-7

Upstream product

• 67-56-1 methanol 
• 672-78-6 methyl p-toluene sulfinate 

Downstream Products

• 116471-84-2 4-Methyl-benzenesulfinic acid (S)-allyl-methyl-amide 
• 116471-85-3 N,N-diallyltoluene-p-sulphinamide 
• 116471-85-3 (R)-N,N-diallyl-p-toluenesulfinamide 
• 111289-39-5 [Isopropyl-((S)-toluene-4-sulfinyl)-amino]-acetic acid tert-butyl ester 
• 116471-84-2 4-Methyl-benzenesulfinic acid (R)-allyl-methyl-amide 
• 103808-56-6 (+)-octadecyl p-tolyl sulphoxide 
• 6873-54-7 N-phenyltoluene-p-sulphinamide 
• 40723-30-6 (+)-(S)-allyl-p-toluenesulphinamide 
• 6873-86-5 (+)-(S)-isopropyl-p-toluenesulphinamide 

Relevant academic research and scientific papers

Optical Resolution of Methyl Phenyl and Benzyl Methyl Sulfoxides and Alkyl Phenylsulfinates by Complexation with Chiral Host Compounds Derived from Tartaric Acid

The title sulfoxides and sulfinates are resolved by complexation with chiral host compounds derived from tartaric acid.

NUCLEOPHILIC SUBSTITUTION AT SULFINYL AND SULFONYL CENTRES: STEREOCHEMICAL AND KINETIC STUDIES

The mechanism and stereochemistry of nucleophilic substitution reactions at sulfur (SN-S) are discussed in the light of experimental results obtained in the author's laboratory.The first part of this short review article is devoted to the acid-catalyzed alcoholysis of chiral sulfinates and sulfinamides.In the second part, the results of kinetic studies of the isotopic chloride-chloride exchange reaction in sulfonyl chlorides are presented.