The Journal of Organic Chemistry · 2007 · 44 citations · 27 references
Natural SciencesChemistryMedicinal ChemistryNatural Product BiosynthesisOrganic ChemistrySolid-state ChemistryHeterocycle SynthesisHeterocyclic ChemistryMacrocycle SynthesisMarine Natural Product BiosynthesisMarine Natural ProductsOrganic SynthesisAsymmetric Heterocycle SynthesisMacrocycle Library SynthesisMacrocyclic Library SynthesisMarine Natural Product DiscoveryMarine Natural Product IsolationNatural Product SynthesisNatural Product Total SynthesisRegioselective Catalysis
A new facile approach toward natural and unnatural indanones has been developed, featuring a solid-supported [2+2+2] cyclotrimerization as the key step. This strategy has been applied to the chemo- and regioselective assembly of indanone arrays and to the total synthesis of a recently isolated indanone marine natural product.
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