181780-95-0

Upstream product

• 5779-99-7 4-methoxybenzo[d][1,3]dioxole-5-carbaldehyde 
• 181780-93-8 2-Benzo[1,3]dioxol-5-yl-N-((R)-1-phenyl-ethyl)-acetamide 
• 2220-16-8 (4-methoxy-benzo[1,3]dioxol-5-yl)-acetonitrile 
• 6845-81-4 3,4-methylenedioxyphenylacetyl chloride 
• 2861-28-1 1,3-benzodioxole-5-acetic acid 
• 108261-13-8 2-methoxy-3,4-methylenedioxybenzyl alcohol 
• 2220-17-9 2-Methoxy-3,4-methylendioxy-benzylchlorid 
• 181780-92-7 (4-Methoxy-benzo[1,3]dioxol-5-yl)-acetyl chloride 
• 181780-94-9 (2-Benzo[1,3]dioxol-5-yl-ethyl)-((R)-1-phenyl-ethyl)-amine 

Downstream Products

• 181931-78-2 marshaline 
• 181780-97-2 (R)-5-(4-Methoxy-benzo[1,3]dioxol-5-ylmethyl)-6-((R)-1-phenyl-ethyl)-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinoline 

Relevant academic research and scientific papers

Asymmetric synthesis of (R)-1-(2-methoxy-3,4-methylenedioxybenzyl)-2-methyl-6,7-methylenedioxy-1,2,3,4- tetrahydroisoquinoline (so-called "fumarizine")

(R)-1-(2-Methoxy-3,4-methylenedioxybenzyl)-2-methyl-6,7-methylenedioxy-1,2, 3,4-tetrahydroisoquinoline (so-called "fumarizine") (1) was synthesized via the stereoselective reduction of the corresponding chiral iminium. ion (11), which was obtained by the