20 research outputs found

    Synthesis in the group of nuphar alkaloids. VII. An easy access to (-)-nupharamine

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    A simple and effective approach to the total synthesis of (-)-nupharamine (I) is presented, which allows to control the stereochemistry at C-3 by epimerization of the ethoxycarbonyl function. The key steps are reductive amination of the respective substituted 1,5-diketone V and enantiomer resolution of piperidine VI using (1S)-(-)-camphanic acid.</jats:p

    The total synthesis of (±)-Nα-methyl-Nβ-acetylphlegmarine

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