29093-70-7

Upstream product

• 29199-18-6 3-(4-methoxyphenyl)pentenedioic anhydride 
• 100-66-3 methoxybenzene 
• 7446-70-0 aluminium trichloride 
• 98-95-3 nitrobenzene 
• 124-38-9 carbon dioxide 
• 16197-83-4 4,4'-dimethoxy-β-methylchalcone 
• 79963-53-4 δ-Hydroxy-δ-(4-hydroxyphenyl)-β-(4-methoxyphenyl)-α,γ-pentadienoic acid δ-lactone 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 109845-17-2 3,5-bis-(4-methoxy-phenyl)-5-phenylhydrazono-valeric acid 
• 65321-71-3 3,5-bis-(4-methoxy-phenyl)-5-oxo-valeric acid 
• 16197-83-4 4,4'-dimethoxy-β-methylchalcone 
• 410542-13-1 4,6-bis-(4-methoxy-phenyl)-thiopyran-2-one 
• 154667-00-2 4,6-bis(4-methoxphenyl)-2H-pyran-2-thione 

Relevant academic research and scientific papers

Carboxylative cyclization of substituted propenyl ketones using CO2: Transition-metal-free synthesis of Α-pyrones

Carbon dioxide is a green carboxylative reagent due to its non-toxic and renewable properties. Described herein is a carboxylative cyclization of substituted 1-propenyl ketones via γ-carboxylation using CO2, which provides an efficient, transit

Reactions of β-(4-Methoxyphenyl)glutaconic Anhydride with Phenolic Ethers: Synthesis of Substituted δ-Hydroxy-α,γ-pentadienoic Acid δ-Lactones and Related Compounds

Condensation of β-(4-methoxyphenyl)glutaconic anhydride (I) with phenetole under Friedel-Crafts conditions furnishes δ-(4-ethoxyphenyl)-δ-hydroxy-β-(4-methoxyphenyl)-α,γ-pentadienoic acid δ-lactone (IIa) and γ-(4-ethoxybenzoyl)-β-(4-methoxyphenyl)crotonic acid (IIIa).A similar condensation of I with diphenyl ether results in the formation of δ-hydroxy-β-(4-methoxyphenyl)-δ-(4-phenoxyphenyl)-α,γ-pentadienoic acid δ-lactone (IIb) and β-(4-methoxyphenyl)-γ-(4-phenoxybenzoyl)crotonic acid (IIIb).Some reactions of II and III have been studied.