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Studies on the syntheses of heterocyclic compounds. Part DXCVII. A synthesis of dienone analogs by electrolytic oxidation
Authors:Tetsuji Kametani  Kozo Shishido  Seiichi Takano
Abstract:
Electrolytic coupling reaction of laudanosine (1) gave the O-methylflavinantine (II). N-Ethoxycarbonylated dihydrostilbene (IVa) gave a rearranged dienone (Va) and N-trifluoro-acetylated dihydrostilbene (IVb) contrastively gave an unrearranged dienone (Vb).
Keywords:
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