Yazarlar

• Altundaş, Ramazan(1)
• Burmaoǧlu, Serdar(1)
• Göiksu, Süleyman(1)
• Maraş, Ahmet(1)
• Seçen, Hasan(1)
• Çelik, Hülya(1)

• MakaleAçık Erişim2009Scopus SJRQ3/r/bayburt/12609
  Synthesis of two alnustone-like natural diarylheptanoids via 4+3 strategy

  Burmaoǧlu, Serdar; Çelik, Hülya; Göiksu, Süleyman; Maraş, Ahmet; Altundaş, Ramazan; Seçen, Hasan

  The first total synthesis of (4E,6E)-1,7-bis(3,4-dihydroxyphenyl)-hepta-4, 6-dien-3-one and an alternative synthesis of (4E,6E)-1,7-bis(4-hydroxyphenyl)- hepta-4,6-dien-3-one, two natural diarylheptanoids, mainly based on Claisen-Schmidt condensation were described. The crucial steps of the syntheses were the condensation of OH-protected 4-aryl-2-butanones with OH-protected 3-aryl-acrylaldehydes by the in situ enamination and then deprotection of OH groups to give the corresponding natural diarylheptanoids.

  AtıfScopus6·WoS5·OpenAlex7

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