883458-49-9

Upstream product

• 247089-85-6 (R)-p-toluenesulfinamide 
• 110-62-3 pentanal 
• 883458-47-7 (R)-(-)-N-pentylidene-p-toluenesulfinamide 
• 883458-48-8 (R_S,R)-(-)-methyl N-(p-toluenesulfinyl)-3-aminoheptanoate 

Downstream Products

• 883458-50-2 (R)-(+)-4-methyl-N-(1-oxoheptan-3-yl)benzenesulfonamide 

Relevant academic research and scientific papers

Asymmetric synthesis of trans-2,5-disubstituted pyrrolidines from enantiopure homoallylic amines. Synthesis of pyrrolidine (-)-197B

Iodocyclization of sulfinimine-derived enantiopure homoallylic sulfonamides affords trans-2,5-disubstituted 3-iodopyrrolidines and represents valuable methodology for the asymmetric synthesis of this important heterocyclic ring system.