• MakaleAçık Erişim2009Scopus SJRQ3
    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.

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