Quantum chemical studies on some potentially tautomeric thiazolidinone derivatives and their thio and azo analogs

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Tokay N., Oegretir C.

ARKIVOC, ss.88-99, 2008 (SCI-Expanded, Scopus) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası:
  • Basım Tarihi: 2008
  • Doi Numarası: 10.3998/ark.5550190.0009.e10
  • Dergi Adı: ARKIVOC
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.88-99
  • Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
  • Eskişehir Osmangazi Üniversitesi Adresli: Evet

Özet

The gas phase semi-empirically calculated relative stability and tautomeric equilibrium values revealed that 2C, 4C, and 5C hydroxy substituted thiazolidinone derivatives prefer oxo forms. The 2C, 4C, and 5C mercapto substituted derivatives also found to prefer the thione forms. On the contrary 2C, 4C, and 5C amino substituted derivatives were found to prefer amino forms.