33139-84-3

Upstream product

• 108-31-6 maleic anhydride 
• 618-36-0 rac-methylbenzylamine 
• 2627-86-3 (S)-1-phenyl-ethylamine 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 

Downstream Products

• 188401-87-8 C₂₆H₂₁NO₃ 
• 60925-76-0 (S)-(-)-α-Methylbenzylmaleimide 
• 89143-34-0 1-(1-Phenyl-ethyl)-3-piperidin-1-yl-pyrrolidine-2,5-dione 
• 89143-22-6 1'-(1-Phenyl-ethyl)-[1,3']bipyrrolidinyl-2',5'-dione 
• 138118-32-8 (3aR,7aS)-5-Methyl-2-(1-phenyl-ethyl)-3a,4,7,7a-tetrahydro-isoindole-1,3-dione 
• 138118-37-3 6-Methoxy-2-(1-phenyl-ethyl)-4-trimethylsilanyloxy-3a,4,7,7a-tetrahydro-isoindole-1,3-dione 
• 138118-38-4 2-(1-Phenyl-ethyl)-5-trimethylsilanyloxy-3a,4,7,7a-tetrahydro-isoindole-1,3-dione 
• 138118-34-0 2-(1-Phenyl-ethyl)-3a,4,6,7,8,9,9a,9b-octahydro-benzo[e]isoindole-1,3-dione 
• 138118-35-1 5-Phenyl-2-(1-phenyl-ethyl)-3a,4,7,7a-tetrahydro-isoindole-1,3-dione 
• 138118-39-5 4-Methoxy-2-(1-phenyl-ethyl)-3a,4,7,7a-tetrahydro-isoindole-1,3-dione 
• 138118-33-9 4-Methyl-2-(1-phenyl-ethyl)-3a,4,7,7a-tetrahydro-isoindole-1,3-dione 
• 106058-59-7 1-(1-Phenyl-ethyl)-3-(4-phenylsulfanyl-phenylamino)-pyrrolidine-2,5-dione 
• 106058-47-3 3-(4-Ethoxy-phenylamino)-1-(1-phenyl-ethyl)-pyrrolidine-2,5-dione 
• 106058-37-1 3-(4-Methoxy-phenylamino)-1-(1-phenyl-ethyl)-pyrrolidine-2,5-dione 

Relevant academic research and scientific papers

Heat-resistant poly(N-(1-phenylethyl)maleimide-co-styrene) microspheres prepared by dispersion polymerization

This article reports on a novel type of polymeric microsphere consisting of poly(N-(1-phenylethyl)maleimide-co-styrene) (poly(N-PEMI-co-St)) and showing remarkable heat resistance. Such microspheres were prepared by dispersion polymerization with 2,2′-azo

Synthesis and reactivity of (1S)-N-(1-phenylethyl)maleimide towards nucleophiles: An application to preparation of chiral pyrroloisothiochroman and pyrrolobenzo[d]thiepine based on π-cationic cyclization

Chiral pyrroloisothiochroman and pyrrolo[d]thiepine were obtained efficiently in four steps from N-alkylated maleimides via, successively, sulfurization, regioselective reduction followed by π-cationic cyclization of the N-acyliminium ion intermediates. These latter, in addition, led to conjugate enamides as a consequences of the dehydration reaction.

Asymmetric cycloaddition of anthrone with n-substituted maleimides with C2-chiral pyrrolidines

Base-catalyzed asymmetric cycloaddition of anthrone with achiral and chiral N-substituted maleimides was carried out in the presence of C2-chiral pyrrolidines in almost quantitative yields. Chiral, non-racemic [4+2] adducts up to 61% ee were produced with achiral N-methyl and N-benzylmaleimide using the chiral catalysts. De's of the adducts up to 38% were observed in the cases of chiral N-substituted maleimides and achiral pyrrolidine, in which the absolute configuration Of the major product was established by X-ray analysis. The combination of chiral maleimides and chiral catalysts afforded the adducts having up to 80% de.

Diastereoselective Diels-Alder reactions between substituted 1,3-butadienes and N-α-methylbenzylmaleimide

The TiCl4 catalyzed reaction between 2-t-butyl-1,3-butadiene and N-α-methylbenzylmaleimide at -65°C affords diastereomeric Diels-Alder adducts in a 15:1 ratio. The structure of the major adduct was determined by x-ray.

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.