34603-53-7

Upstream product

• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 67019-56-1 4'-methoxy-3,4,5,6-tetrahydro-[1,1'-biphenyl]-3-ol 
• 17159-98-7 3-(4-methoxyphenyl)-2-cyclohexen-1-one 
• 117360-96-0 3-<(1-methylpropyl)oxy>-2-cyclohexen-1-one 
• 34603-52-6 1-[2-(dimethylamino)ethyl]-4'-methoxy-2,3-dihydro-[1,1′-biphenyl]-4(1H)-one 
• 67019-53-8 1-(2-(dimethylamino)ethyl)-4′-methoxy-1,2,3,4-tetrahydro-[1,1′-biphenyl]-4-ol 
• 67019-52-7 2-(4′-methoxy-4-oxo-1,2,3,4-tetrahydro-[1,1′-biphenyl]-1-yl)-N,N-dimethylacetamide 
• 67019-55-0 2-(4'-methoxy-1,2,3,4-tetrahydro-[1,1'-biphenyl]-1-yl)-N,N-dimethylacetamide 
• 81254-94-6 5,5-ethylenedioxy-2-(4'-phenylmethoxyphenyl)cyclohexanone 
• 121537-70-0 5,5-ethylenedioxy-2-(4'-phenylmethoxyphenyl)cyclohexanol 
• 121537-69-7 4,4-ethylenedioxy-1-(4'-phenylmethoxyphenyl)cyclohexene 
• 40167-10-0 2-[4-(benzyloxy)phenyl]acetaldehyde 
• 121537-68-6 2-dimethylaminomethylcyclohexyl acetate 
• 81254-96-8 (1RS,2SR)-5,5-ethylenedioxy-2-formylmethyl-2-(4'-phenylmethoxyphenyl)cyclohexyl acetate 

Relevant academic research and scientific papers

Concise Total Syntheses of (±)-Joubertiamine, (±)- O -Methyljoubertiamine, (±)-3′-Methoxy-4′- O -methyljoubertiamine, (±)-Mesembrane, and (±)-Crinane

A method to access cis-3a-aryloctahydroindole alkaloids has been developed through a key strategy involving Eschenmoser-Claisen rearrangement of allylalcohol. This approach gives us an opportunity to access the all-carbon quaternary center required for ci

A Synthesis of Seco-mesembrane Alkaloids, (+/-)-Joubertiamine, (+/-)-Joubertinamine, and (+/-)-Epijoubertinamine

A synthesis of seco-mesembrane alkaloids, (+/-)-joubertiamine (4), (+/-)-joubertinamine (5), and (+/-)-epijoubertinamine (6), was accomplished starting with 2-allyl-2-aryl-5,5-ethylenedioxycyclohexanones (10 and 3), which are readily available by allylati