330800-28-7

Upstream product

• 32293-48-4 N-(5-benzyloxy-2-bromo-4-methoxybenzyl)-N-methyl-(4-benzyloxyphenyl)acetamide 
• 330800-27-6 N-(5-benzyloxy-2-bromo-4-methoxybenzyl)-(4-benzyloxyphenyl)acetamide 
• 330800-26-5 5-benzyloxy-2-bromo-4-methoxybenzylamine 
• 6547-53-1 2-[4-(benzyloxy)benzyl]acetic acid 
• 39188-62-0 2-(4-(benzyloxy)phenyl)acetyl chloride 
• 13255-21-5 1-(benzyloxy)-4-bromo-5-(chloromethyl)-2-methoxybenzene 
• 13397-01-8 [5-(benzyloxy)-2-bromo-4-methoxyphenyl]methanol 

Downstream Products

• 55708-63-9 4-(4-benzyloxyphenyl)-7-benzyloxy-6-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline 
• 26996-80-5 4-(4-hydroxyphenyl)-7-hydroxy-6-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline 

Relevant academic research and scientific papers

Palladium-catalyzed intramolecular δ-lactam formation of aryl halides and amide-enolates: Syntheses of cherylline and latifine

(Matrix presented) Palladium-catalyzed intramolecular carbon-carbon bond formation of aryl halides and amide-enolates gave 4-arylisoquinoline derivatives in good yields, which were further converted into the isoquinoline alkaloids cheryllme and latifine.