107613-10-5

Upstream product

• 124-38-9 carbon dioxide 
• 92210-76-9 (S_S)-3-[(4-methylphenyl)sulfinyl]furan-2(5H)-one 
• 865205-69-2 (3aS,6aR,(S)S)-6a-[(4-methylphenyl)sulfinyl]-3,3a,4,6a-tetrahydro-6H-furo[3,4-c]pyrazol-6-one 
• 865205-70-5 (3aR,6aS,(S)S)-6a-[(4-methylphenyl)sulfinyl]-3,3a,4,6a-tetrahydro-6H-furo[3,4-c]pyrazol-6-one 

Downstream Products

• 865205-76-1 (3S,3aS,6aR,S_S)-3,3a-dimethyl-6a-[(4-methylphenyl)sulfinyl]-3,3a,4,6a-tetrahydro-6H-furo[3,4-c]pyrazol-6-one 
• 865205-75-0 (3R,3aS,6aR,(S)S)-3,3a-dimethyl-6a-[(4-methylphenyl)sulfinyl]-3,3a,4,6a-tetrahydro-6H-furo[3,4-c]pyrazol-6-one 
• 865205-73-8 (3aS,6aR,(S)S)-3a-methyl-6a-[(4-methylphenyl)sulfinyl]-3,3a,4,6a-tetrahydro-6H-furo[3,4-c]pyrazol-6-one 
• 865205-74-9 (3aR,6aS,(S)S)-3a-methyl-6a-[(4-methylphenyl)sulfinyl]-3,3a,4,6a-tetrahydro-6H-furo[3,4-c]pyrazol-6-one 

Relevant academic research and scientific papers

A new entry to enantiopure polysubstituted cyclopropanes: Stereoselective denitrogenation of sulfinylpyrazolines under Yb(OTf)3 catalysis

Chemoselective and completely stereoselective denitrogenation of optically pure pyrazolines, derived from 3-sulfinylfuran-2(5H)-ones, into cyclopropanes can be achieved under substoichiometric Yb(OTf)3 catalysis. Reactions evolve in almost quan

1,3-Dipolar cycloadditions of diazoalkanes to activated sulfoxides: Influence of Lewis acids

The reactions of diazomethane and diazoethane with (S)-3-p- tolylsulfinylfuran-2(5H)-one (3) and its 4-methyl derivative (4) have been studied. The sulfinyl group was able to completely control the π-facial selectivity of all these reactions, which decrea

AN EFFICIENT SYNTHESIS OF CHIRAL 2-(p-TOLYLSULFINYL)-2-BUTENOLIDES

A high yield, two-step synthesis of enantiomerically pure 2-(p-tolylsulfinyl)-2-butenolides has been developed.The method is applicable to the preparation of butenolides having a variety of substituents in the 3-position.