Publication | Closed Access
Highly diastereroselective synthesis of dihydrofurans and dihydropyrroles viapyridine catalyzed formal [4+1] annulation
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Citations
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References
2010
Year
Pyridine-catalyzed Ylide CyclizationChemical EngineeringEngineeringCatalytic AmountHigh DiastereoselectivitiesOrganic ChemistryCatalysisChemistryDiastereroselective SynthesisHeterocycle ChemistrySynthesis MethodAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
A pyridine-catalyzed ylide cyclization affording dihydrofurans and dihydropyrroles has been developed. In the presence of a catalytic amount of pyridine and Fe(Tcpp)Cl, α-ylidene-β-diketones and α,β-unsaturated imines react with diazoacetates providing dihydrofurans and dihydropyrroles respectively, in up to 96% yield with high diastereoselectivities.
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