82939-70-6

Upstream product

• 82939-69-3 methyl 1-(2-ethylbut-1-en-4-yl)-2,6-dimethoxycyclohexa-2,5-diene-1-carboxylate 
• 23010-02-8 2-(chloromethyl)-1-butene 
• 4435-54-5 2-Methylene-1-butanol 
• 1708-98-1 3-methylenepentan-1-ol 
• 82939-66-0 methyl 2,6-dimethoxy-2,5-cyclohexadiene-1-carboxylate 
• 98770-72-0 Toluene-4-sulfonic acid 3-methylene-pentyl ester 
• 82939-71-7 2-Ethyl-4-iodobut-1-ene 
• 92269-61-9 2-methylenebutyl 4-methylbenzenesulfonate 
• 58310-18-2 1,4-dihydro-2,6-dimethoxybenzoic acid 

Downstream Products

• 82939-73-9 1,5-Dimethoxy-6-(2-methoxy-ethoxymethoxymethyl)-6-(3-methylene-pentyl)-cyclohexa-1,4-diene 
• 82939-74-0 Acetic acid 2,6-dimethoxy-1-(3-methylene-pentyl)-cyclohexa-2,5-dienylmethyl ester 
• 80900-51-2 2-<(methoxymethoxy)methyl>-2-(3-oxopentyl)cyclohexane-1,3-dione 
• 82939-79-5 2-(2-ethylbut-1-en-4-yl)-2-methoxymethylcyclohexane-1,3-dione 
• 82939-83-1 2-methoxymethyl-2-(3-oxopentyl)cyclohexane-1,3-dione 
• 82939-77-3 2-(2-ethylbut-1-en-4-yl)-2-<<(2-methoxyethoxy)methoxy>methyl>cyclohexane-1,3-dione 
• 82939-81-9 2-<<(2-methoxyethoxy)methoxy>methyl>-2-(3-oxopentyl)cyclohexane-1,3-dione 
• 98770-73-1 2-(2-ethylbut-1-en-4-yl)-2-<(methoxymethoxy)methyl>cyclohexane-1,3-dione 
• 82939-82-0 2-acetoxymethyl-2-(3-oxopentyl)cyclohexane-1,3-dione 
• 82939-78-4 2-acetoxymethyl-2-(2-ethylbut-1-en-4-yl)cyclohexane-1,3-dione 
• 82939-75-1 3-(2-ethylbut-1-en-4-yl)-2,4-dimethoxy-3-methoxymethylcyclohexa-1,4-diene 

Relevant academic research and scientific papers

Synthesis and Absolute Stereochemistry of Optically Active Wieland-Miescher Ketone Analogues bearing an Angular Protected Hydroxymethyl Group

Four optically active Wieland-Miescher ketone analogues, bearing an angular protected hydroxymethyl group, have been synthesised through eight steps starting from 2,6-dimethoxybenzoic acid in good chemical and optical yields, and the absolute stereochemis

Synthesis of Wieland-Miescher Ketone Analogues bearing an Angular Protected Hydroxymethyl Group

Wieland-Miescher ketone analogues (1) and (2), bearing an angular protected hydroxymethyl group, have been prepared by alkylation of the lithiated methyl 2,6-dimethoxycyclohexa-2,5-diene-1-carboxylate.