1373869-66-9

Upstream product

• 70-55-3 toluene-4-sulfonamide 
• 1373869-69-2 C₁₁H₁₅IO₆ 
• 1357181-64-6 (Z)-ethyl 2-iodo-4-(4-methylphenylsulfonamido)-4-oxobut-2-enoate 
• 1357181-45-3 (2E,4E)-3-ethoxycarbonyl-5-(3-thienyl)-N-(p-toluenesulfonyl)-2,4-pentadienamide 
• 1357181-62-4 (Z)-4-ethoxy-3-iodo-4-oxobut-2-enoic acid 

Relevant academic research and scientific papers

Palladium-catalyzed asymmetric 6-endo cyclization of dienamides with substituent-driven activation

Chiral 2-piperidinone compounds with various C-6 substituents were successfully synthesized via a Pd-catalyzed asymmetric 6-endo cyclization of dienamides, which were evidently activated by both N-p-toluenesulfonyl and C-3 ester substituents.