Publication | Closed Access
Synthesis of Indoles by Intermolecular Cyclization of Unfunctionalized Nitroarenes and Alkynes: One‐Step Synthesis of the Skeleton of Fluvastatin
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Citations
33
References
2009
Year
Bioorganic ChemistryEngineeringOrganic ChemistryChemistryHeterocycle ChemistryIntermolecular CyclizationMedicinal ChemistryDerivativesBiochemistryDiversity-oriented SynthesisFluorous SynthesisIndole SkeletonPharmacologyNatural Product SynthesisRu 3Biomolecular EngineeringUnfunctionalized NitroarenesNatural SciencesOne‐step SynthesisDimethyl CarbonateDerivative (Chemistry)Synthetic Chemistry
Abstract The addition of Ru 3 (CO) 12 , dimethyl carbonate, or both to the reaction mixture improves the selectivity of the palladium/phenanthroline‐catalyzed reaction of nitroarenes, arylalkynes, and CO to give 3‐arylindoles. When 4‐fluorophenylacetylene and nitrobenzene are used as substrates, the indole skeleton of Fluvastatin and other pharmaceutically active compounds is obtained in one step.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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