Natural Product Communications · 2013 · 13 citations · 18 references
PharmacyMedicinal ChemistryDrug DiscoveryNatural Product BiosynthesisSynthetic Medicinal ChemistryFlavonoid BiosynthesisNatural Product Drug DiscoveryPhenylpropanoid BiosynthesisPlant Natural Product BiosynthesisTerpenoid BiosynthesisClaisen CondensationClaisen RearrangementFruit FlavonoidsLignan BiosynthesisNatural Product Total SynthesisPlant-derived Natural ProductsSaponin BiosynthesisWittig Reaction
The concise, efficient synthesis of alpha-mangostin is described in eight simple steps with 8.3% overall yield. Highlights include a practical approach to construct the isopentene groups and other diverse groups at C-2 and C-8 of the xanthene skeleton through Claisen rearrangement and Wittig reaction. Meanwhile the first total synthesis of beta-mangostin is presented with a similar approach.
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Yoshihito Nakagawa, Munekazu Iinuma, Tomoki Naoe et al. · Bioorganic & Medicinal Chemistry · 2007 · 165 citations
José Pedraza‐Chaverrí, Laura María Reyes-Fermín, Eva Guadalupe Nolasco-Amaya et al. · Experimental and Toxicologic Pathology · 2008 · 126 citations
Pandima Devi Sampath, Vijayaraghavan Kannan · Journal of Biochemical and Molecular Toxicology · 2007 · 125 citations
Medicine, Cardiology, Pharmacology +16