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The total synthesis of (±)-Cepharatine ASeipp, Charles Aaron 30 September 2014 (has links)
The hasubanan alkaloid cepharatine A, was efficiently synthesized in 8 steps from commercially available starting materials in overall 16% yield. Highlighted in this synthesis, is a tandem phenolic alkylation – annulation which formed both a quaternary center as well as an unsaturated ring. This key step allowed for rapid construction of the core of the molecule. Subsequent reductive amination and acid catalyzed cyclization afforded the title compound. / text
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