113756-46-0

Upstream product

• 113756-45-9 8-benzyloxy-1-(3',4'-dibenzyloxybenzyl)-1,2,3,4-tetrahydro-7-methoxy-N-methylisoquinoline 
• 50-00-0 formaldehyd 
• 1699-60-1 (3,4-bis-benzyloxyphenyl)acetonitrile 
• 56522-51-1 2-bromo-5-hydroxy-4-methoxyphenethylamine 

Relevant academic research and scientific papers

The Biosynthesis of the Cularine Alkaloids

In order to study the cularine biosynthesis, L-tyrosine (L-18), tyramine (20), L-DOPA (L-19) and dopamine (21) were synthesized and fed to Corydalis claviculata and Sarcocapnos crassifolia plants, which are rich source

Sythetic Approaches to Cularines. III. Nucleophilic Addition and Substitution

Attempts to induce the formation of the dibenzoxepine ring of cularine compounds by generating an electron-deficient system in ring C of an 8-hydroxybenzylisoquinoline met with failure.Attack by C-8 phenol on a "p-quinone methide" intermediate afforded be