10381-69-8

Upstream product

• 10381-69-8 (-)-p-tolyl mesityl sulfoxide 
• 1517-82-4 (1R,2S,5R,SS)-(-)-menthyl p-toluenesulfinate 
• 2633-66-1 2-mesitylmagnesium bromide 
• 106-45-6 para-thiocresol 
• 108-67-8 1,3,5-trimethyl-benzene 
• 911820-09-2 3-[(4-methylphenyl)sulfinyl]propanoic acid tert-butyl ester 
• 139139-80-3 bis(2,4,6-trimethylphenyl)iodonium triflate 
• 77333-17-6 (+)-(R)-mesityl p-tolyl sulphoxide 
• 4294-57-9 para-methylphenylmagnesium bromide 

Downstream Products

• 20268-15-9 (-)-(S)-mesityl p-tolyl sulphoxide 
• 77333-17-6 (+)-(R)-mesityl p-tolyl sulphoxide 

Relevant academic research and scientific papers

Direct C-H Thiolation for Selective Cross-Coupling of Arenes with Thiophenols via Aerobic Visible-Light Catalysis

An aerobic metal-free, visible-light-induced regioselective thiolation of phenols with thiophenols is reported. The cross-coupling protocol exhibits great functional group tolerance and high regioselectivity. Mechanistic studies reveal that the disulfide

Transition-Metal-Free Arylations of In-Situ Generated Sulfenates with Diaryliodonium Salts

A transition-metal-free arylation of sulfenate anions generated from β-sulfinyl esters with diaryliodonium salts was developed. In this process, a new C-S bond is formed under mild reaction conditions providing a wide range of S,S-diaryl and S-alkyl S-aryl sulfoxides.

Optically Active Selenoxides: Chromatographic Separation and Absolute Configuration

Asymmetric diaryl selenoxides were optically resolved by medium pressure column chromatography on an optically active column.The absolute configuration of the optically active selenoxides was estimated by comparison of their circular dichroism spectra wit

Use of Carbohydrates in the Preparation of Optically Active Sulphoxides

The diastereomeric sulphinate esters formed from arenesulphinyl chlorides and 1,2:5,6-di-O-cyclohexylidene-D-glucofuranose afford optically active sulphoxides on treatment with Grignard reagents.