33531-75-8

Upstream product

• 32209-88-4 3a-benzo[1,3]dioxol-5-yl-1-benzyl-(3ar,7ac)-octahydro-indol-6-one 
• 32209-88-4 (3aS*,7aS*)-1-benzyl-3a,4,5,6,7,7a-hexahydro-3a-(3',4'-methylenedioxyphenyl)-6-oxoindoline 
• 114047-02-8 2-allyl-5,5-ethylenedioxy-2-(3',4'-methylenedioxyphenyl)cyclohexanol 
• 114046-99-0 8-Allyl-8-benzo[1,3]dioxol-5-yl-1,4-dioxa-spiro[4.5]decan-7-one 
• 114047-04-0 (1R*,2S*)-5,5-ethylenedioxy-2-formylmethyl-2-(3',4'-methylenedioxyphenyl)cyclohexyl acetate 
• 114047-05-1 (1R*,2S*)-2-allyl-5,5-ethylenedioxy-2-(3',4'-methylenedioxyphenyl)cyclohexyl acetate 

Downstream Products

• 10279-81-9 (+/-)-epielwesine 
• 10279-81-9 (+/-)-elwesine 

Relevant academic research and scientific papers

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