725744-01-4

Upstream product

• 1896-62-4 (E)-benzalacetone 
• 791799-82-1 (E)-N-allyl-1-(4-fluorophenyl)methanimine 
• 65300-29-0 (E)-4-(4-fluorophenyl)but-3-en-2-one 

Downstream Products

• 910561-99-8 meso-2,6-bis(4-fluorophenyl)piperidin-4-one 

Relevant academic research and scientific papers

Stereoselective synthesis of meso- and cis-2,6-diarylpiperidin-4-ones catalyzed by L-proline

A convenient stereoselective preparation of meso- and cis-2,6- diarylpiperidin-4-ones has been developed by aza-Diels-Alder reaction catalyzed by L-proline from simple and commercially available starting materials. Georg Thieme Verlag Stuttgart.

Proline-catalyzed imino-Diels-Alder reactions: Synthesis of meso-2,6-diaryl-4-piperidones

Amine-catalyzed imino-Diels-Alder reactions of acyclic α,β- unsaturated ketones with imines have been developed. L-Proline catalyzed the in situ generation of 2-amino-1,3-butadienes to provide a stereoselective synthesis of meso-2,6-diaryl-4-piperidones i

An imino-Diels-Alder route to meso-2,6-disubstituted-4-piperidones

A convenient stereoselective preparation of meso-2,6-disubstituted-4- piperidones has been developed by imino-Diels-Alder reaction of 2-amino-1,3-butadienes with imines in the presence of catalytic amount of Cu(TfO)2.