90832-96-5

Upstream product

• 10539-50-1 diethyl 2-benzoylsuccinate 
• 90833-15-1 3-benzoyl-3-ethoxycarbonylpropionic acid 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 261957-14-6 3-benzoyl-3-(ethoxycarbonyl)propionic acid tert-butyl ester 

Downstream Products

• 901764-32-7 1-benzyl-2-oxo-5-phenyl-2,3-dihydro-1H-pyrrole-4-carboxylic acid ethyl ester 
• 128318-56-9 3,5,6-Triphenyl-1H-furo<3,4-c>pyrrole-1,4(5H)-dione 
• 871667-88-8 ethyl 1,2-diphenyl-4-[1-phenyl-1-(phenylamino)methylidene]-4,5-dihydro-5-oxopyrrole-3-carboxylate 
• 871667-87-7 4-[1-Hydroxy-1-phenyl-meth-(Z)-ylidene]-5-oxo-1,2-diphenyl-4,5-dihydro-1H-pyrrole-3-carboxylic acid ethyl ester 
• 827606-92-8 ethyl 4,5-dihydro-5-oxo-1,2-diphenylpyrrole-3-carboxylate 

Relevant academic research and scientific papers

Synthesis of substituted butenolides by the ring closing metathesis of two electron deficient olefins: a general route to the natural products of paraconic acids class

A variety of allyl acrylates possessing electron-withdrawing groups undergo RCM using the second generation Grubbs' catalyst in the presence of a Lewis acid resulting in diverse butenolides in high isolated yields. This methodology provides a general rout

"On water" catalytic enantioselective sulfenylation of deconjugated butyrolactams

The first catalytic enantioselective α-sulfenylation of deconjugated butyrolactams has been developed using dimeric cinchona alkaloids as catalysts in a water-enriched reaction medium. Highly substituted and densely functionalized γ-lactams, bearing a qua

Unsaturated lactones: Synthesis and applications

An easy approach to the synthesis of substituted unsaturated lactones is described, and the reactions of these compounds with nucleophiles leading to the formation of useful intermediates are reported.

Synthesis of 3-Ethoxycarbonyl-3-buten-4-olides and 3-Ethoxycarbonyl-4-butanolides

This paper describes a synthesis of 3-acyl-2-alkyl-3-ethoxycarbonylpropanoic acids from ethyl 2-oxoalkanoates and 2-bromoalkanoic acids.These acids are cyclised via intramolecular dehydratation to give 2,4-dialkyl-3-ethoxycarbonyl-3-buten-4-olides or are

SYNTHESE DE β-ETHOXYCARBONYL γ-LACTONES

β-ethoxycarbonyl β, γ-insaturated γ-lactones 2 are easily prepared by dehydration of β-acyl β-ethoxycarbonyl α-alkyl propionic acids.Otherwise the condensation of these acids with allylzinc reagents produces β-ethoxycarbonyl γ-lactones 3 with a β-ethyleni