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Biomimetic Total Synthesis of Cruentaren A via Aromatization of Diketodioxinones

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posted on 2012-04-06, 00:00 authored by Marianne Fouché, Lisa Rooney, Anthony G. M. Barrett
The total synthesis of cruentaren A, a biologically active resorcylate natural product, is reported. The aromatic unit was constructed via late-stage cyclization and aromatization from a diketodioxinone intermediate and macrocyclization using Fürstner ring-closing alkyne metathesis.

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