107095-03-4

Upstream product

• 67089-90-1 (R)-3-benzoyl-4-hydroxymethyl-2,2-dimethyl-thiazolidine 
• 67089-83-2 3-benzoyl-2,2-dimethyl-4(R)-methoxycarbonylthiazolidine 
• 19907-58-5 4(R)-(methoxycarbonyl)-2,2-dimethylthiazolidine hydrochloride 
• 98-88-4 benzoyl chloride 
• 95095-15-1 2,2-dimethyl-3-benzoyl-4-methoxycarbonylthiazolidine 

Relevant academic research and scientific papers

ASYMMETRIC INDUCTION TO SULFUR ATOM: STEREOCONTROLLED S-OXIDATION OF THIAZOLIDINES

Oxidation of (2R,4R)-2,4-disubstituted thiazolidines with m-CPBA affords the trans sulfoxide exclusively.Oxidation of (2R,4R)-4-hydroxymethyl thiazolidines with Ti(OiPr)4/TBHP, however, favors to give the cis sulfoxide.

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