114047-07-3

Upstream product

• 70779-49-6 4,4-ethylenedioxy-1-(3',4'-dimethoxyphenyl)cyclohexene 
• 114046-91-2 2-(3,4-Dimethoxy-phenyl)-5-oxo-hexanal 
• 5703-21-9 3,4-dimethoxyphenylacetaldehyde 
• 70779-48-5 4-(3,4-Dimethoxy-phenyl)-cyclohex-3-enone 

Downstream Products

• 114047-00-6 2-cyanoethyl-5,5-ethylenedioxy-2-(3',4'-dimethoxyphenyl)cyclohexanone 
• 70779-51-0 5,5-ethylenedioxy-2-(3',4'-dimethoxyphenyl)cyclohexanone 

Relevant academic research and scientific papers

Catalytic asymmetric hydrogenation of α-arylcyclohexanones and total synthesis of (-)-α-lycorane

An efficient catalytic asymmetric hydrogenation of racemic α-arylcyclohexanones with an ethylene ketal group at the 5-position of the cyclohexane ring via dynamic kinetic resolution has been developed, giving chiral α-arylcyclohexanols with two contiguous

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