209455-66-3Relevant academic research and scientific papers
Five-membered 2,3-Dioxoheterocycles. XLIV. Synthesis and Nucleophilic Reactions of 5-(β-Styryl)-2,3-dihydro-2.3-furandione
Shurov,Porvintsev,Kosvintseva,Andreichikov
, p. 1116 - 1124 (2007/10/03)
Cyclization of cinnamoylpyruvic acid results in 5-(β-styryl)-2,3-dihydro-2.3-furandione. Its reactions were studied with nucleophilic reagents: water, alcohols, acetone oxime, amines, o-aminophenol, and o-phenylenediamine. Geometric and electronic structure of cinnamoylpyruvic acid, 5-(β-styryl)-2,3-dihydro-2.3-furandione, and mechanism of formation of methyl cinnamoylpyruvate was investigated by quantum-chemical LCAO MO method in AMI approximation.
