Reactions of 4-benzoyl-5-[(E)-2-phenyl-1-ethenyl]-2,3-dihydro-2,3-furandione with aromatic aminonucleophiles

Durmaz N., Onal Z., Altural B.

ASIAN JOURNAL OF CHEMISTRY, cilt.18, sa.2, ss.1261-1266, 2006 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 18 Sayı: 2
  • Basım Tarihi: 2006
  • Dergi Adı: ASIAN JOURNAL OF CHEMISTRY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1261-1266
  • Anahtar Kelimeler: 2,3-dihydro-2,3-furandione, hexadienoic acids, aminonucleophiles, nucleophlic addition reactions, CYCLIC OXALYL COMPOUNDS, FUNCTIONALIZED 1H-PYRIMIDINES, HETEROCYCLIC-COMPOUNDS, CYCLIZATION REACTIONS, SCHIFF-BASES, DERIVATIVES, ACID, 4-BENZOYL-2,3-DIOXO-5-PHENYL-2,3-DIHYDROFURAN, THERMOLYSIS
  • Erciyes Üniversitesi Adresli: Evet

Özet

4-Benzoyl-5-[(E)-2-phenyl-1-ethenyl]-2,3-dihydro-2-,3-furandi one (1) reacts with various aminonucleophiles (2a-g) and gives the hexadienoic acid derivatives (6-phenyl-3-benzoyl-arylamino-2-ogo3,5-hexadieonic acids) (3a-g). The structures of the synthesized compounds were determined by being interpreted by their elemental analysis and IR, H-1- and C-13-NMR spectra.