67089-89-8

Upstream product

• 95095-15-1 2,2-dimethyl-3-benzoyl-4-methoxycarbonylthiazolidine 
• 94-36-0 dibenzoyl peroxide 
• 67089-83-2 3-benzoyl-2,2-dimethyl-4(R)-methoxycarbonylthiazolidine 
• 67089-92-3 L-(-)-2,2-dimethylthiazolidine-4-carboxylic acid hydrochloride salt 
• 98-88-4 benzoyl chloride 
• 95542-74-8 3-benzoyl-2,2-dimethyl-thiazolidine-4-carboxylic acid 
• 57704-00-4 3-benzoyl-2,2-dimethylthiazolidine-4R-carboxylic acid 
• 100429-04-7 3-benzoyl-2,2-dimethyl-5-hydroxy-4-methoxycarbonylthiazolidine 
• 19907-58-5 4(R)-(methoxycarbonyl)-2,2-dimethylthiazolidine hydrochloride 

Downstream Products

• 104654-64-0 3-Benzoyl-2,2-dimethyl-2,3-dihydro-thiazole-4-carboxylic acid methyl ester 
• 67324-85-0 (4R)-3-benzoyl-5t-(6-benzoylamino-purin-9-yl)-2,2-dimethyl-thiazolidine-4r-carboxylic acid methyl ester 

Relevant academic research and scientific papers

SYNTHESIS AND REACTIONS OF CYCLIC α-HYDROXY SULFIDES

Stable, optically active α-hydroxy sulfides are prepared in high yields by reduction of corresponding α-hydroperoxy sulfides obtained by stereospecific photohydroperoxidation of optically active thiazolidine derivatives.A few reactions as well as spectros

NEW SYNTHETIC UTILITY OF SINGLET OXYGEN IN SULPHIDE PHOTO-OXIDATION. SELECTIVE AND STEREOSPECIFIC HYDROXYLATION α TO SULPHUR OF 4-SUBSTITUTED 3-BENZOYL-2,2-DIMETHYLTHIAZOLIDINES

Direct hydroxylation α to sulphur was accomplished in singlet oxygenation of thiazolidine derivatives.Photo-oxidation of 4-substituted 3-benzoyl-2,2-dimethylthiazolidines in aprotic solvents below 0 deg C gave the corresponding 5-hydroxy derivatives quant