Reactions of 4-Benzoyl-5-[(E)-2-phenyl-1-ethenyl]-2,3-dihydro-2,3-furandione with Aromatic Aminonucleophiles
Corresponding Author(s) : Behzat Altural
altural@erciyes.edu.tr
Asian Journal of Chemistry,
Vol. 18 No. 2 (2006): Vol 18 Issue 2
Abstract
4-Benzoyl-5-[(E)-2-phenyl-1-ethenyl]-2,3-dihydro-2-,3-furandione (1) reacts with various aminonucleophiles (2a–g) and gives the hexadienoic acid derivatives (6-phenyl-3-benzoylarylamino-2-oxo-3,5-hexadieonic acids) (3a–g). The structures of the synthesized compounds were determined by being interpreted by their elemental analysis and IR, 1H- and 13C-NMR spectra.
Keywords
Hexadienoic acids
Aminonucleophiles
Nucleophlic addition reactions
2,3-Dihydro-2,3-furandione
Durmaz, N., Onal, Z., & Altural, B. (2010). Reactions of 4-Benzoyl-5-[(E)-2-phenyl-1-ethenyl]-2,3-dihydro-2,3-furandione with Aromatic Aminonucleophiles. Asian Journal of Chemistry, 18(2), 1261–1266. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/21134
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