50845-51-7

Upstream product

• 59214-81-2 4-Benzyl-1-phenyl-1,4-dihydro-3-(2H)isoquinolinone 
• 17507-05-0 1-phenyl-1,4-dihydro-3(2H)-isoquinolinone 
• 100-52-7 benzaldehyde 
• 105950-22-9 4-Benzylidene-1-phenyl-1,4-dihydro-3(2H)-isoquinolinone 

Downstream Products

• 87748-23-0 C₂₆H₁₉NO₄ 
• 87748-23-0 C₂₆H₁₉NO₄ 
• 108276-82-0 1-benzyl-4,7-diphenyl-10-methyl-4,10-diazabenzo-<8,9>-tricyclo<2,2,0,3>-8-undecene-3,5,11-trione 
• 108304-71-8 4-benzyl-2-methyl-1-phenyl-3(2H)-isoquinolinone 

Relevant academic research and scientific papers

Mechanism of the Condensation Reaction Between 1-Aryl- and Heteroaryl-1,4-dihydro-3(2H)-isoquinolinones and Aldehydes

4-Benzylidene-1-phenyl-1,4-dihydro-3(2H)-isoquinolinone, the intermediary product of the carbonyl condensation reaction between 1-phenyl-1,4-dihydro-3(2H)-isoquinolinone and benzaldehyde, rearranges in the presence of an equivalent quantity of sodium hydr

Reactions of 1,4-Dihydro-3-(2H)benzoisoquinolinones with Aldehydes in the Presence of a Strong Base. Condensation and Aromatization as Competing Reactions

In reactions of 1-phenyl-1,4-dihydro-3-(2H)benzoisoquinolinones with benzaldehyde in the presence of a strong base, the final result can be ring substitution with aromatization or only aromatization of the starting isoquinolinone, depending on the positio