108391-29-3

Upstream product

• 2216-51-5 (-)-menthol 
• 2901-92-0 p-chlorophenylsulfinyl chloride 
• 98-60-2 4-chlorobenzenesulfonyl chloride 
• 100-03-8 4-chlorobenzenesulfinic acid 

Downstream Products

• 308810-23-3 (+)-(R)-p-Chlorophenyl-2-phenylethyl-sulfoxide 
• 121794-59-0 t-Butyl (R_S)-p-chlorophenylsulphinylacetate 
• 125416-26-4 10-dicyclohexylsulfamoyl-D-isobornyl (R)(+)-4-chlorophenylsulfinylacetate 
• 125416-27-5 10-dicyclohexylsulfamoyl-D-isobornyl (S)(-)-4-chlorophenylsulfinylacetate 
• 934-73-6 (S)-4-chlorophenyl methyl sulfoxide 
• 28227-63-6 (R)-1-chloro-4-(methylsulfinyl)benzene 
• 308810-24-4 (-)-(R,R)-p-Chlorophenyl-1-bromo-2-phenylethyl sulfoxide 
• 222016-68-4 (R,R)-p-Chlorophenyl-1-chloro-2-phenylethyl sulfoxide 
• 109574-73-4 ((R)-4-Chloro-benzenesulfinyl)-acetonitrile 

Relevant academic research and scientific papers

An efficient and novel method for the synthesis of sulfinate esters under solvent-free conditions

The present letter describes a reliable one-stage process for the preparation of sulfinate esters from the corresponding sulfinic acid and alcohols in the presence of N,N′-dicyclohexylcarbodiimide (DCC) under solvent-free conditions.

An improved and efficient procedure for the preparation of chiral sulfinates from sulfonyl chloride using triphenylphosphine

An improved procedure of the Sharpless method for the preparation of chiral sulfinates by triphenylphosphine is described. A mixture of sulfonyl chlorides and diacetone-D-glucose or l-menthol in the presence of triethylamine was treated with triphenylphos

A convenient and highly diastereoselective synthesis of optically active sulfinate esters from sulfonyl chlorides under solid state conditions

A manipulatively simple and rapid method for synthesis of chiral sulfinate esters 1 and 2 from sulfonyl chloride and trimethyl phosphite in solid phase conditions supported on silica gel is described. The chemical yields are good to excellent and diastereoselectivity is high.