247118-53-2

Upstream product

• 10313-60-7 3,4-dimethoxyphenylacetyl chloride 
• 93-40-3 (3,4-Dimethoxyphenyl)acetic acid 
• 106-95-6 allyl bromide 
• 234089-44-2 (+)-<1'S,2'S>-N-(2'-hydroxy-1'-methyl-2'-phenylethyl)-2-(3,4-dimethoxyphenyl)-N-methylacetamide 

Downstream Products

• 773835-29-3 (+)-(3S,4S)-N-benzyl-3-(3,4-dimethoxyphenyl)-6,7-dimethoxy-4-(2-propenyl)-1,2,3,4-tetrahydroisoquinoline 
• 247118-71-4 (+)-(3S,4S)-N-benzyl-3-(3,4-methylenedioxyphenyl)-6,7-dimethoxy-4-(2-propenyl)-1,2,3,4-tetrahydroisoquinoline 
• 247118-63-4 (-)-(1S,2S)-N-benzyl-1,2-bis(3,4-dimethoxyphenyl)-4-pentenylamine 
• 247118-66-7 (-)-(1S,2S)-N-benzyl-2-(3,4-dimethoxyphenyl)-1-(3,4-methylenedioxyphenyl)-4-pentenylamine 
• 247118-62-3 (+)-(S)-2-(3,4-dimethoxyphenyl)-1-(3,4-methylenedioxyphenyl)-4-penten-1-one 
• 247118-59-8 (+)-(S)-1,2-bis(3,4-dimethoxyphenyl)-4-penten-1-one 
• 247118-56-5 (+)-(S)-2-(3,4-dimethoxyphenyl)-4-pentenoic acid 

Relevant academic research and scientific papers

The first stereocontrolled synthesis of 12-methylhexahydrobenzo [c]phenanthridine alkaloids

12-Methyl B/C hexahydrobenzo[c]phenanthridines have been synthesized stereoselectively starting from chiral nonracemic 2-aryl-4-pentenoic acids prepared by asymmetric allylation of (+)-(S,S)-pseudoephedrine-based arylacetamide enolates. Subsequent transfo