104375-70-4

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 84812-14-6 (E)-2-((4-p-tolyl)but-3-en-1-yl)isoindoline-1,3-dione 
• 10285-80-0 N-tosyl-3-butenylamine 
• 31614-66-1 tributyl(p-tolyl)stannane 

Relevant academic research and scientific papers

Alkene Oxyamination Using Malonoyl Peroxides: Preparation of Pyrrolidines and Isoxazolidines

Treatment of homoallylic N-tosyl amines or allylic N-tosyl hydroxylamines with 1.5 equiv of a malonoyl peroxide provides a stereoselective method to access functionalized pyrrolidines and isoxazolidines. This metal free alkene oxyamination proceeds in 50-

Synthesis of Five- and Six-Membered Nitrogen Heterocycles via a Palladium(II)-Catalyzed Cyclization of Unsaturated Amides

Palladium(II)-catalyzed arylation of N-4-pentenyl-p-toluenesulfonamides 2 with ArSn(n-Bu)3 under oxidative conditions (CuCl2 in ether) provides either 2-arylpiperidines 5 or N-(chloro-5-arylpentyl)-p-toluenesulfonamides 6 depending on the kind of arylatin