Experiments directed towards the synthesis of (±)-flourensic acid are described, starting with readily available bicyclic structures. Eremophilone was ultimately converted into the (+)-acid in eight steps, providing corroboration of the proposed structure and configuration.
J. N. Herron and A. R. Pinder, J. Chem. Soc., Perkin Trans. 1, 1983, 161 DOI: 10.1039/P19830000161
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