4796-05-8

Upstream product

• 108-31-6 maleic anhydride 
• 60-15-1 2-amino-1-phenylpropane 

Downstream Products

• 89143-23-7 1'-(1-Methyl-2-phenyl-ethyl)-[1,3']bipyrrolidinyl-2',5'-dione 
• 89143-35-1 1-(1-Methyl-2-phenyl-ethyl)-3-piperidin-1-yl-pyrrolidine-2,5-dione 
• 89143-11-3 N-(α-Methyl-β-phenylethyl)maleimide 
• 106058-60-0 1-(1-Methyl-2-phenyl-ethyl)-3-(4-phenylsulfanyl-phenylamino)-pyrrolidine-2,5-dione 
• 106058-48-4 3-(4-Ethoxy-phenylamino)-1-(1-methyl-2-phenyl-ethyl)-pyrrolidine-2,5-dione 
• 106058-38-2 3-(4-Methoxy-phenylamino)-1-(1-methyl-2-phenyl-ethyl)-pyrrolidine-2,5-dione 

Relevant academic research and scientific papers

An efficient synthesis of substituted isoxazolopyrroloisoquinolines via diastereoselective N-acyliminium ion cyclization

A simple and efficient strategy was developed for the synthesis of fused pyrrolo[2,1-a]isoquinoline ring systems. The 5- and 6-substituted isoxazolopyrroloisoquinolines were readily prepared via diastereoselective N-acyliminium ion cyclization of 5-(1-R(or 2-R)-substituted-2-phenylethyl)-6-hydroxytetrahydro-4H-pyrrolo[3,4-d]isoxazol-4-ones derived from the corresponding bicyclic dihydroisoxazoles.

Synthesis of N-Aryl/heteroaryl/-substituted-methyl-&α-(p-substituted anilino)succinimides as Antituberculosis Agents

A series of N-Aryl/heteroaryl/substituted-methyl-α-(p-substituted anilino)succinimides (II) have been prepared and screened in vitro against H37Rv strain of Mycobacterium tuberculosis.Some of these compounds exhibit activity upto 0.39 μg/ml concentration.

Synthesis of N-Aryl/substituted-methyl/heteroaryl-&α-pyrrolidino/piperidino Succinimides as Antituberculosis Agents

A series of N-Aryl/substituted-methyl/heteroaryl-α-pyrrolidino- and piperidino-succinimides (II) have been prepared and screened in vitro against H37Rv strain of Mycobacterium tuberculosis.Some of these compounds exhibit activity upto 1.56 μg/ml concentration.