192190-40-2

Upstream product

• 105170-18-1 [5-(benzyloxy)-2-methoxyphenyl]acetonitrile 
• 52329-05-2 5-benzyloxy-2-methoxyphenyl methanol 
• 192190-39-9 5-benzyloxy-2-methoxyphenylacetic acid 

Downstream Products

• 192190-41-3 N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-N-((S)-1-phenylethyl)-2-(5-benzyloxy-2-methoxyphenyl)acetamide 
• 192190-42-4 7-Benzyloxy-1-(5-benzyloxy-2-methoxy-benzyl)-6-methoxy-2-((S)-1-phenyl-ethyl)-3,4-dihydro-isoquinolinium 
• 192190-43-5 (S)-1-(5-benzyloxy-2-methoxybenzyl)-N-((S)-phenylethyl)-7-benzyloxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline 
• 192190-44-6 (S)-1-(5-hydroxy-2-methoxybenzyl)-7-hydroxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline 

Relevant academic research and scientific papers

Asymmetric synthesis of ( S)-l-(5-hydroxy-2-methoxybenzyl)-7-hydroxy-6-methoxy-2-methyl-1,2,3,4- tetrahydroisoquinoline (so-called "dehassiline")

Optically active, (S)-l-(5-hydroxy-2methoxybenzyl )-7-h.ydroxy-6-methoxy-2-meth.yl-l ,2,3,4tetrahydroisoquinoline (so-called "dehassiline") (1) was synthesized via highly stereoselective reduction of the 3,4-dihydroisoquinolinium ion possessing a chiral a