Organic Letters · 2004 · 33 citations · 5 references
PharmacyBiochemistryBiologyBiocatalysisBioorganic ChemistryNatural Product BiosynthesisBiomimetic SynthesisRetrosynthetic AnalysisBiomimetic Cascade ReactionsBiomimetic Diels-alder ReactionsBiomimetic RearrangementFunctional ReassignmentNatural Product Total SynthesisOxidative Biosynthetic TransformationsSinglet Oxygen ChemistrySinglet Oxygen Formation
[reaction: see text] The first total synthesis of litseaverticillols B (1), E (2), I (4), and J (5) as well as the structural reassignment of litseaverticillol E (2) have been achieved by means of a biomimetic sequence of transformations during which a [4 + 2]-initiated reaction cascade and an ene reaction, both involving singlet oxygen ((1)O(2)), formed key steps. The reassignment of the structure of litseaverticillol E (3) to include an allylic hydroperoxide provides strong support for our biogenetic hypothesis.
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