101471-67-4

Upstream product

• 85907-71-7 3-(dimethylamino)-2-(3,4-dimethoxyphenyl)prop-2-en-1-al 
• 99706-75-9 3--2-(3,4-dimethoxyphenyl)prop-2-en-1-al 
• 121537-76-6 2-carboxymethyl-5,5-ethylenedioxy-2-(3',4'-dimethoxyphenyl)cyclohexyl acetate 
• 99706-75-9 3--2-(3,4-dimethoxyphenyl)prop-2-en-1-al 
• 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 
• 102737-69-9 4-(3,4-Dimethoxy-phenyl)-4-((E)-2-methoxy-2-phenylsulfanyl-vinyl)-cyclohex-2-enone 
• 70779-54-3 Acetic acid (7R,8S)-8-(3,4-dimethoxy-phenyl)-8-(2-oxo-ethyl)-1,4-dioxa-spiro[4.5]dec-7-yl ester 
• 70779-53-2 Acetic acid (7R,8S)-8-allyl-8-(3,4-dimethoxy-phenyl)-1,4-dioxa-spiro[4.5]dec-7-yl ester 

Downstream Products

• 121537-80-2 [1-(3,4-Dimethoxy-phenyl)-4-hydroxy-cyclohex-2-enyl]-acetic acid methyl ester 
• 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 
• 121537-82-4 4-carboxymethyl-4-(3',4'-dimethoxyphenyl)-2-cyclohexanol 
• 71357-60-3 racemic epijoubertinamine 
• 71294-61-6 (+/-)-epijoubertinamine 
• 21104-34-7 N-methyl-3a-<3,4-(dimethoxy)phenyl>-2,3,3a,4,5,6,7,7a-octahydroindole-2,6-dione 

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

A Concise Synthetic Route to Polyfunctional γ-Ketoester Derivatives via Methoxy(phenylthio)methyl-lithium

The α,β-unsaturated O,S-acetals obtained via the reaction of methoxyphenylthiomethyl-lithium with 3-alkoxyenones are readily convertible into structurally diverse γ-ketoesters by way of an efficient alkylation-hydrolysis sequence.