770686-91-4

Upstream product

• 913985-88-3 4-bromo-2,3-dimethoxy-1-benzyloxybenzene 
• 69471-04-1 4-benzyloxy-2,3-dimethoxybenzaldehyde 
• 52800-47-2 3-(benzyloxy)benzene-1,2-diol 
• 52249-83-9 1-(benzyloxy)-2,3-dimethoxybenzene 
• 173789-50-9 4-benzyloxy-2,3-dimethoxy-β-nitrostyrene 

Downstream Products

• 913985-89-4 N-[2-(4-benzyloxy-2,3-dimethoxy-phenyl)-ethyl]-acetamide 
• 1173352-60-7 2-(5-benzyloxy-2-bromophenyl)-N-(4-benzyloxy-2,3-dimethoxyphenethyl)acetamide 
• 1173352-64-1 2-(2-bromo-4,5-methylenedioxyphenyl)-N-(4-benzyloxy-2,3-dimethoxyphenethyl)acetamide 
• 1173352-33-4 2-(2-bromophenyl)-N-(4-benzyloxy-2,3-dimethoxyphenethyl)acetamide 
• 1173352-56-1 2-(2-bromo-4,5-dimethoxyphenyl)-N-(4-benzyloxy-2,3-dimethoxyphenethyl)acetamide 
• 913985-93-0 (7-allyloxy-5,6-dimethoxy-1-methylene-3,4-dihydro-1H-isoquinolin-2-yl)-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-methanone 
• 913985-91-8 N-[2-(4-allyloxy-2,3-dimethoxy-phenyl)-ethyl]-acetamide 
• 913985-90-7 N-[2-(4-hydroxy-2,3-dimethoxy-phenyl)-ethyl]-acetamide 

Relevant academic research and scientific papers

First total syntheses of (±)-isopiline, (±)-preocoteine, (±)-oureguattidine and (±)-3-methoxynordomesticine and the biological activities of (±)-3-methoxynordomesticine

A convenient and economical synthesis of 4-hydroxy-2,3- dimethoxybenzaldehyde has been developed. This was used as the starting material for the first total syntheses of (±)-isopiline, (±)-preocoteine, (±)-oureguattidine and (±)-3-methoxynordomesticine in

The first total synthesis of (±)-annosqualine by means of oxidative enamide-phenol coupling: pronounced effect of phenoxide formation on the phenol oxidation mechanism

The first total synthesis of a spiro-isoquinoline alkaloid, (±)-annosqualine, was established by employing an enamide-phenol coupling of a 1-methylene-1,2,3,4-tetrahydroisoquinoline derivative with a hypervalent iodine reagent, where the formation of the