Journal of Heterocyclic Chemistry · 2008 · 12 citations · 46 references
Natural SciencesChemistryMedicinal ChemistryBioorganic ChemistryOrganic ChemistrySynthetic Medicinal ChemistryCarbonyl ChemistryHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisIndole ChemistryIndole SynthesisPyrrolidine SynthesisReactivitySynthetic Analogues
Abstract magnified image This review presents a survey of the synthetic methods and reactions of 3‐pyrrolidinones I (R = H, alkyl, acyl, ester; R 1 = H, alkyl, cyano, ester, etc). 3‐Pyrrolidinones are synthetically versatiles substrate, as they can be used for synthesis of a large variety of heterocyclic compounds, such as indoles and 5‐deazapteroic acid analogues and as a raw material for drug synthesis. The high reactivity of an active methylene group next to the carbonyl of the pyrrolidine ring is useful for various syntheses.
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