29879-69-4

Upstream product

• 550-44-7 N-methylphthalimide 
• 67-64-1 acetone 

Downstream Products

• 104563-07-7 3-(2-hydroxyphenyl)-2-methylisoindolin-1-one 
• 86770-02-7 3-Benzyl-2,3-dihydro-2-methyl-1H-isoindol-1-one 
• 566151-95-9 N-methyl-3-methyl-3-phenylthiophthalimidine 
• 566151-94-8 3-allyl-2-methyl-3-phenylsulfanyl-2,3-dihydro-isoindol-1-one 
• 566151-96-0 3-benzyl-2-methyl-3-phenylsulfanyl-2,3-dihydro-isoindol-1-one 
• 1373426-75-5 (E)-2-methyl-3-(2-phenylethenyl)isoindolin-1-one 
• 1373426-77-7 3-(2,2-diphenylethenyl)-2-methylisoindolin-1-one 
• 1383455-38-6 C₃₁H₂₉NO₅ 
• 1383455-48-8 1,1-di(hydroxylmethyl)-3-(N-methylisoindolin-1-onyl)-4-phenyl-1,2-dihydronaphthalene 
• 1383455-44-4 3-[(4,4-diphenyl-dihydro-furan-2-ylidene)-phenyl-methyl]-2-methyl-2,3-dihydro-isoindol-1-one 
• 1383455-43-3 2-methyl-3-(2,2,5-triphenyl-pent-4-ynyloxy)-2,3-dihydro-isoindol-1-one 
• 1383455-37-5 3-(N-benzylisoindolin-1-onyl)-4-phenyl-1-tosyl-1,2-dihydroquinoline 
• 1373426-76-6 2-methyl-3-(2-phenyl-2-propenyl)isoindolin-1-one 
• 1215067-51-8 3-hydroxy-2-methyl-7-phenylselanyl-2,3-dihydro-isoindol-1-one 

Relevant academic research and scientific papers

PROCESS FOR THE ASYMMETRIC HYDROGENATION OF IMIDES

The present disclosure provides a process for the mono-reduction of one or more imide moieties in a compound comprising contacting the compound with hydrogen gas and a catalyst comprising a transition metal hydride in the presence of a base, under conditi

The photodecarboxylative addition of carboxylates to phthalimides: Scope and limitations

Intermolecular photoinduced decarboxylative additions of a series of alkylcarboxylates to N-substituted phthalimides gave the corresponding hydroxyphthalimidines in moderate to high yields of 39-89%. The potassium salt of 1-adamantanecarboxylic acid predominately underwent simple decarboxylation when irradiated in the presence of N-methylphthalimide. In case of phthalimides carrying suitable leaving groups within the N-side chain, decarboxylation, retro-Aldol cleavage or decarbonylation preceded the intermolecular addition step.