70779-54-3

Upstream product

• 70779-52-1 2-allyl-5,5-ethylenedioxy-2-(3',4'-dimethoxyphenyl)cyclohexanone 
• 70779-53-2 Acetic acid (7R,8S)-8-allyl-8-(3,4-dimethoxy-phenyl)-1,4-dioxa-spiro[4.5]dec-7-yl ester 
• 114047-03-9 2-allyl-5,5-ethylenedioxy-2-(3',4'-dimethoxyphenyl)cyclohexanol 
• 70779-53-2 (1R*,2S*)-2-allyl-5,5-ethylenedioxy-2-(3',4'-dimethoxyphenyl)cyclohexyl acetate 

Downstream Products

• 114047-08-4 C₄₈H₅₇NO₉ 
• 71610-13-4 (+/-)-N,O-diacetyljoubertinamine 
• 71610-13-4 (+/-)-N,O-diacetyljoubertinamine 
• 74045-71-9 (1RS,4SR)-4-(3',4'-dimethoxyphenyl)-4-(N-methylcarbamoylmethyl)-2-cyclohexenol 
• 74045-71-9 (1SR,4SR)-4-(3',4'-dimethoxyphenyl)-4-(N-methylcarbamoylmethyl)-2-cyclohexenol 
• 121537-77-7 (1RS,2SR)-5,5-ethylenedioxy-2-(N-methylamidomethyl)-2-(3',4'-dimethoxyphenyl)cyclohexyl acetate 
• 121537-78-8 [(7R,8S)-7-Acetoxy-8-(3,4-dimethoxy-phenyl)-1,4-dioxa-spiro[4.5]dec-8-yl]-acetic acid methyl ester 
• 121537-80-2 [1-(3,4-Dimethoxy-phenyl)-4-hydroxy-cyclohex-2-enyl]-acetic acid methyl ester 
• 121537-82-4 4-carboxymethyl-4-(3',4'-dimethoxyphenyl)-2-cyclohexanol 
• 21104-33-6 cis-3a-(3',4'-dimethoxyphenyl)-1-methyloctahydroindole-2,6-dione 
• 87014-19-5 3a-(3,4-Dimethoxy-phenyl)-hexahydro-benzofuran-2,6-dione 
• 101471-67-4 4-(carbomethoxymethyl)-4-(3,4-dimethoxyphenyl)cyclohex-2-en-1-one 
• 71357-60-3 racemic epijoubertinamine 
• 71294-61-6 (+/-)-epijoubertinamine 

Relevant academic research and scientific papers

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

Synthesis of Sceletium and Amaryllidaceae Alkaloids, (+/-)-Mesembrine and (+/-)-Dihydromaritidine, (+/-)-Epidihydromaritidine, (+/-)-Elwesine, and (+/-)-Epielwesine

The alkylation of 2-arylcyclohexanones (12b and 6) with alkyl halides or acrylonitrile and 50percent aq. sodium hydroxide in the presence of a phase-transfer catalyst (18-crown-6) was found to give readily 2-alkyl-2-arylcyclohexanones (14 and 16) in fair