13255-21-5

Upstream product

• 100-39-0 benzyl bromide 
• 100-44-7 benzyl chloride 
• 2973-59-3 2-bromoisovanillin 
• 6451-86-1 5-benzyloxy-2-bromo-4-methoxybenzaldehyde 
• 13397-01-8 [5-(benzyloxy)-2-bromo-4-methoxyphenyl]methanol 

Downstream Products

• 330800-27-6 N-(5-benzyloxy-2-bromo-4-methoxybenzyl)-(4-benzyloxyphenyl)acetamide 
• 330800-28-7 4-(4-benzyloxyphenyl)-7-benzyloxy-6-methoxy-2-methyl-3-oxo-1,2,3,4-tetrahydroisoquinoline 
• 330800-26-5 5-benzyloxy-2-bromo-4-methoxybenzylamine 
• 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 
• 32293-48-4 N-(5-benzyloxy-2-bromo-4-methoxybenzyl)-N-methyl-(4-benzyloxyphenyl)acetamide 

Relevant academic research and scientific papers

Fused tricyclic compounds and application thereof in medicaments

The invention relates to fused tricyclic compounds and an application thereof in medicaments, and in particular to an application of the fused tricyclic compounds in medicaments for treating and/or preventing hepatitis B. In particular, the invention rela

FUSED TRICYCLIC COMPOUNDS AND USES THEREOF IN MEDICINE

The present invention relates to a fused tricyclic compound and application thereof in medicine, especially as a medicament for the treatment and/or prevention of hepatitis B. Specifically, the present invention relates to a compound having Formula (I) or

NOVEL 6,7-DIHYDROPYRIDO[2,1-A]PHTHALAZIN-2-ONES FOR THE TREATMENT AND PROPHYLAXIS OF HEPATITIS B VIRUS INFECTION

The invention provides novel compounds having the general formula: wherein R1 to R6 are as described herein, compositions including the compounds and methods of using the compounds.

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.