Synthesis of the Core Structure of Acutumine

The tricyclic core of the bioactive natural product acutumine has been synthesized. Key steps include an oxidative phenolic coupling to form
a masked o-benzoquinone, an anionic oxy-Cope rearrangement to construct an all-carbon quaternary center, and a Michael-type cyclization
to form an amine-bearing quaternary carbon. The target compound exists in solution as an enol, in contrast to related compounds that are
ketones. A model explaining these observations is presented.