63327-14-0

Upstream product

• 21382-82-1 (carbethoxyethylidene)triphenylphosphorane 
• 4693-91-8 4-methoxyphenyl-acetic chloride 
• 103-80-0 phenylacetyl chloride 

Downstream Products

• 1089678-73-8 4-allyl-1-(4'-methoxylphenyl)-3-methyl-1,2,6-heptatrien-4-ol 
• 1044510-86-2 C₁₈H₂₂O₅ 
• 1092696-50-8 2-fluoro-4-(4-methoxyphenyl)-2-methylbut-3-ynoic acid ethyl ester 
• 1227751-53-2 ethyl 4-(4-methoxyphenyl)-2-methyl-4-(2,4,6-trimethoxyphenyl)but-2(E)-enoate 
• 1204199-75-6 ethyl 4-(p-methoxyphenyl)-2-methyl-3-phenyl-3(E)-butenoate 
• 1204199-68-7 ethyl 2,3-dimethyl-4-(p-methoxyphenyl)-3(Z)-butenoate 
• 1337937-13-9 C₁₈H₂₂O₄ 
• 1380396-92-8 ethyl (2E)-5-benzoyl-4-(4-methoxyphenyl)-2-methyl-6-oxo-6-phenylhex-2-enoate 
• 1280135-97-8 ethyl 2-methyl-4-(4-methoxyphenyl)-4-(1-tosyl-1H-indol-3-yl)but-2(E)-enoate 
• 1280135-88-7 ethyl 2-methyl-4-(4-methoxyphenyl)-4-(1-tosyl-1H-indol-3-yl)but-2(Z)-enoate 
• 1280136-05-1 ethyl 2-methyl-4-(4-methoxyphenyl)-4-(1-acetyl-1H-indol-3-yl)but-2(E)-enoate 
• 1042097-02-8 ethyl 2-(1'-(4''-methoxyphenyl)-1'(E)-propen-2'-yl)-2-methyl-4-pentenoate 
• 1042096-85-4 ethyl 2-(1'-(4''-methoxyphenyl)-1'(Z)-propen-2'-yl)-2-methyl-4-pentenoate 

Relevant academic research and scientific papers

Ferric chloride hexahydrate-catalyzed highly regio- And stereoselective conjugate addition reaction of 2,3-allenoates with grignard reagents: An efficient synthesis of β,γ-alkenoates

Ferric chloride hexahydrate was shown to be an efficient catalyst for the conjugate addition of 2,3-allenoates with alkyl-, aryl-, or vinyl-Grignard reagents to synthesize polysubstituted β,γ-unsaturated alkenoates with high regio- and stereoselectivity.

Highly regioselective fluorination and iodination of alkynyl enolates

(Chemical Equation Presented) A simple yet efficient approach to various functionalized quaternary α-alkynyl α-fluoro esters and γ-iodoallenoates from readily available allenoates through an alkynyl enolate intermediate generated by LDA is presented. Reac

Palladium-catalyzed alkylation of vinyl oxiranes with substituted allenes. Direct access to bifunctionalized allylic alcohols

The first palladium-catalyzed alkylation of vinyl oxiranes with substituted allenes to form functionalized allylic alcohols is described. The reaction of activated allenes 5 with vinyl oxiranes 1 in the presence of catalytic amounts of Pd(PPh3)

Hypolipidemic allene carboxylic acids

The compounds are 4-aryl substituted buta-2,3-dienoic acids and esters thereof which may also be lower alkyl-substituted at any of the 2- and 4-positions, e.g., 4-(p-methoxyphenyl)-2-methyl-buta-2,3-dienoic acid. The compounds are useful as pharmaceutical