81038-45-1

Upstream product

• 93-17-4 3,4-dimethoxyphenylacetonitrile 
• 773837-37-9 sodium cyanide 
• 222622-91-5 4-bromo-5-bromomethyl-2-methoxyphenol 
• 4468-58-0 3-hydroxy-4-methoxyphenylacetonitrile 

Downstream Products

• 81038-48-4 2-bromo-4-methoxy-5-hydroxylphenylacetic acid 
• 6451-85-0 5-benzyloxy-2-bromo-4-methoxyphenylacetonitrile 
• 892805-32-2 N-(4'-benzyloxy-3'-methoxyphenylethyl)-2-(2-bromo-5-hydroxy-4-methoxyphenyl)acetamide 
• 892804-31-8 2,10-di(benzyloxy)-3,9-dimethoxy-5,6,12,12a-tetrahydroindolo[2,1-a]isoquinoline 
• 892804-24-9 2,10-di(benzyloxy)-3,9-dimethoxy-5,6-dihydroindolo[2,1-a]isoquinoline 
• 227088-17-7 7-benzyloxy-1-(5'-benzyloxy-2'-bromo-4'-methoxybenzyl)-6-methoxy-3,4-dihydroisoquinoline 
• 13425-04-2 5-benzyloxy-4-methoxy-2-bromophenylacetic acid 
• 13232-98-9 N-(4'-benzyloxy-2-bromo-4-methoxyphenyl)-N-(4'-benzyloxy-3'-methoxyphenylethyl)acetamide 
• 1131-94-8 homoisovanillic acid 
• 58116-06-6 (+/-)-6'-Bromo-N-norreticuline 
• 56952-05-7 (2-bromo-5-hydroxy-4-methoxy-phenyl)-acetic acid methyl ester 
• 81038-51-9 2-(2-Bromo-5-hydroxy-4-methoxy-phenyl)-N-[2-(4-hydroxy-3-methoxy-phenyl)-ethyl]-acetamide 
• 1344720-62-2 2-bromo-5-(2,2-dimethylpropanoyloxy)-4-methoxy-phenyl-acetonitrile 
• 1344720-71-3 (3S)-(E)-N-Boc-N-[2-[5-(2,2-dimethyl-propanoyl-oxy)-2-(3-tert-butyl dimethylsilyloxy-but-1-enyl)-4-methoxy-phenyl]ethyl]-amine 

Relevant academic research and scientific papers

Stereoselective synthesis of tetrahydroisoquinoline alkaloids: (-)-trolline, (+)-crispin A, (+)-oleracein e

Tetrahydroisoquinoline alkaloids, (S)-(-)-trolline, (R)-(+)-crispin A, and (R)-(+)-oleracein E, have been synthesized stereoselectively from the both enantiomers of common intermediate (S)-4 and (R)-4. The key step in the synthesis include a stereoselecti

The palladium-catalyzed preparation of condensed tetracyclic heterocycles and their application to the synthesis of rac-mangochinine

Dihydroisoquinoline derivatives and their analogues, prepared by the Bischler-Napieralsky reaction, were converted to their indole-fused derivatives. Scope and limitations of the palladium-catalyzed reaction, proceeding through the tautomeric enamine forms of these compounds, were studied and the process was extended to the preparation of racemic mangochinine. Georg Thieme Verlag Stuttgart.