Angewandte Chemie · 2015 · 59 citations · 44 references
PharmacyChemistryMedicinal ChemistryNatural Product BiosynthesisOrganic ChemistrySynthetic Medicinal ChemistryHeterocyclic ChemistryOxidation ReactionsPlant Natural Product BiosynthesisRetrosynthetic AnalysisSteroid StructureTerpenoid BiosynthesisBaeyer-villiger OxidationNatural Product Total SynthesisRadical CyclizationRing-forming ReactionsSecondary MetabolitesTotal Synthesis-derived AnaloguesTriterpene Biosynthesis
Abstract Limonoids are highly oxygenated C13α‐triterpenes and common secondary metabolites. Several hundred congeners have been isolated to date. The first total synthesis of (±)‐limonin, the flagship congener of the limonoids, is now reported and features 1) a tandem radical cyclization generating the BCD ring system with the C13α configuration that is essential to the limonoids and a Robinson annulation to construct the limonoid androstane framework, 2) a singlet‐oxygen cycloaddition and a Baeyer–Villiger oxidation to synthesize the highly oxidized D ring, and 3) a Suárez reaction to construct the unique AA′ ring system.
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Biological activity of limonoids from the rutales
Donald E. Champagne, Opender Koul, Murray B. Isman et al. · Phytochemistry · 1992 · 451 citations