2082-28-2

Upstream product

• 2398-37-0 3-methoxyphenyl bromide 
• 502-42-1 cycloheptanone 

Downstream Products

• 75209-54-0 (E)-1-(3-methoxyphenyl)cyclohept-1-en 
• 2082-29-3 {3-[1-(3-Methoxy-phenyl)-cycloheptyloxy]-propyl}-dimethyl-amine 
• 107620-60-0 cyclohex-1-en-1-yl(3-methoxyphenyl)methanone 
• 2914-77-4 (±)-(1R,2S)-2-(dimethylaminomethyl)-1-(3-methoxyphenyl)cyclohexanol 
• 27203-92-5 cis-tramadol 
• 75210-20-7 3-((1R,6S,10S)-10-Methylamino-bicyclo[4.3.1]dec-1-yl)-phenol; hydrobromide 
• 75209-78-8 (1S,6R,7R,10R)-6-(3-Methoxy-phenyl)-10-methylamino-bicyclo[4.3.1]decan-7-ol 
• 75209-78-8 9-endo-hydroxy-1-(m-methoxyphenyl)-10-endo-methylaminobicyclo<4.3.1>decane 
• 75209-63-1 10-endo-amino-9-endo-hydroxy-1-(m-methoxyphenyl)bicyclo<4.3.1>decane 
• 75210-00-3 10-endo-amino-9-endo-hydroxy-1-(m-hydroxyphenyl)bicyclo<4.3.1>decane 
• 75209-85-7 [(1R,6S,10R)-1-(3-Methoxy-phenyl)-bicyclo[4.3.1]dec-10-yl]-methyl-amine 
• 75209-85-7 [(1R,6S,10S)-1-(3-Methoxy-phenyl)-bicyclo[4.3.1]dec-10-yl]-methyl-amine 
• 75209-71-1 10-endo-amino-1-(m-methoxyphenyl)bicyclo<4.3.1>decane 
• 75209-65-3 5-aminomethyl-1-(m-methoxyphenyl)-1-cyclononene 

Relevant academic research and scientific papers

Biomimetic synthesis of Tramadol

Tramadol has recently been isolated from the roots and bark of Nauclea latifolia. A plausible biosynthetic pathway has been proposed and the product-precursor relationship has been probed by 13C position-specific isotope analysis. By further exploring this pathway, we demonstrate that a key step of the proposed pathway can be achieved using mild conditions that mimic in vivo catalysis.