88741-41-7

Upstream product

• 2011-06-5 2-benzyloxy-3-methoxybenzaldehyde 
• 593-51-1 methylamine hydrochloride 
• 100-39-0 benzyl bromide 
• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 

Downstream Products

• 88741-44-0 2-[(2-Benzyloxy-3-methoxy-benzyl)-methyl-amino]-1-phenyl-ethanol 
• 1453172-78-5 4-(benzyloxy)-5-methoxy-2-methylisoindolin-1-one 
• 344864-13-7 2-{[(2-Hydroxy-2-phenyl-ethyl)-methyl-amino]-methyl}-6-methoxy-phenol 
• 88776-68-5 7-Methoxy-2-methyl-4-phenyl-1,2,3,4-tetrahydro-isoquinolin-8-ol 

Relevant academic research and scientific papers

Synthesis and structure–activity relationships of aristoyagonine derivatives as brd4 bromodomain inhibitors with x-ray co-crystal research

Epigenetic regulation is known to play a key role in progression of anti-cancer therapeutics. Lysine acetylation is an important mechanism in controlling gene expression. There has been increasing interest in bromodomain owing to its ability to modulate t

Synthesis of dibenzoxepine lactams via a Cu-catalyzed one-pot etherification/aldol condensation cascade reaction: Application toward the total synthesis of aristoyagonine

A general synthesis of dibenzoxepine lactams has been developed using a one-pot Cu-catalyzed etherification/aldol condensation cascade reaction. The reaction of 4-hydroxyisoindolin-1-one with a wide range of 2-bromobenzaldehydes in the presence of a copper catalyst provided various aristoyagonine derivatives in good yields.