188447-84-9

Upstream product

• 123-72-8 butyraldehyde 
• 153277-56-6 C₁₃H₂₅NOSSi₂ 
• 188447-91-8 (S)-p-toluenesulfinimide 
• 1517-82-4 (-)-menthyl p-toluenesulfinate 

Downstream Products

• 6600-40-4 L-Norvaline 
• 401789-15-9 (3S,4R)-3-(phenylsulfonyl)-4-[(S)-(p-tolylsulfinyl)amino]hept-1-ene 
• 497237-98-6 tert-butyl (2S,3S)-1-[(S)-4-methylbenzenesulfinyl]-3-propylaziridine-2-carboxylate 
• 497237-96-4 methyl (2S,3S)-1-[(S)-4-methylbenzenesulfinyl]-3-propylaziridine-2-carboxylate 
• 170956-17-9 (S)-1-[(4-methylphenyl)sulfonyl]-2-propylaziridin 

Relevant academic research and scientific papers

Asymmetric thio-Michael/nucleophilic addition domino reaction with chiral N-sulfinimines

(Chemical Equation Presented) Optically active N-sulfinimines underwent stereoselective Michael/nucleophilic addition domino reaction triggered by magnesium thiolate to give α-phenylthiomethyl-β-(N-sulfinylamino) esters in high diastereomeric excess. The

Synthesis of enantiopure sulfinimines (Thiooxime S-oxides) catalyzed by Yb(OTf)3 from p-toluenesulfinamide and aldehydes in mild reaction conditions

(Chemical Equation Presented) Enantiomerically pure sulfinimines as important building blocks in the asymmetric synthesis of amine derivatives are prepared in good to excellent yields from chiral p-toluene-sulfinamide with aromatic, heteroaromatic, and al

Asymmetric synthesis of sulfinimines: Chiral ammonia imine synthons

Two Andersen-type procedures for the preparation of enantiopure sulfinimines 1 (R=H) in better than 95% ee from nitriles and aldehydes are described.