38849-39-7

Upstream product

• 100-39-0 benzyl bromide 
• 621-59-0 isovanillin 
• 38849-38-6 3-(benzyloxy)-2-bromo-4-methoxybenzaldehyde 

Downstream Products

• 229017-38-3 (3-Benzyloxy-2-bromo-4-methoxyphenyl)methyl 4-benzyloxybenzoate 
• 38849-40-0 3-benzyloxy-2-bromo-4-methoxybenzyl chloride 
• 38849-41-1 3-benzyloxy-2-bromo-4-methoxybenzyl cyanide 
• 229017-35-0 N-Diphenylphosphinoylmethyl-N-methyl-2-(4-benzyloxybenzoyl)-4-methoxy-3-benzyloxybenzamide 
• 229017-42-9 2-(4-Benzyloxybenzoyl)-4-methoxy-3-benzyloxybenzoic acid 
• 1027841-47-9 5-benzyloxy-4-(4-benzyloxy-phenyl)-6-methoxy-2-methyl-1,2-dihydro-isoquinoline 
• 229017-33-8 4-(4-Benzyloxyphenyl)-6-methoxy-5-benzyloxy-1(2H)-isoquinolone 
• 229017-40-7 3-Benzyloxy-2-(4-benzyloxybenzoyl)-4-methoxybenzaldehyde 
• 97549-48-9 (+/-)-latifine 
• 330800-30-1 N-(3-benzyloxy2-bromo-4-methoxybenzyl)-(4-benzyloxyphenyl)acetamide 
• 330800-31-2 N-(3-benzyloxy-2-bromo-4-methoxybenzyl)-N-methyl-(4-benzyloxyphenyl)acetamide 
• 330800-29-8 3-benzyloxy-2-bromo-4-methoxybenzylamine 

Relevant academic research and scientific papers

Asymmetric total synthesis of (S)-isocorydine

The asymmetric total synthesis of (S)-isocorydine, a potential drug for the cure of hepatocellular carcinoma, is described. Asymmetric transfer hydrogenation of 3,4-dihydroisoquinoline using a chiral Ru(II) catalyst was applied to the synthesis of isocory

First total synthesis of the pavine alkaloid (±)-neocaryachine and its optical resolution

The first total synthesis of (±)-neocaryachine (1) was achieved using a radical cyclization to produce the dibenzo-9-azabicyclo[3.3.1]nonane pavine skeleton, following a Bischler-Napieralski reaction to construct an intermediate benzylisoquinoline. The resulting racemic mixture was separated by chiral column chromatography to provide pure (+)- and (?)-1.