Publication | Closed Access
The First Asymmetric Intramolecular <i>Stetter</i> Reaction. Preliminary Communication
295
Citations
14
References
1996
Year
EngineeringBiochemistryEnantiomeric ExcessesNatural SciencesDiversity-oriented SynthesisOrganic ChemistryPreliminary CommunicationCatalysisReaction IntermediateChemistryHeterocycle ChemistryAsymmetric CatalysisAccessible 4‐Enantioselective SynthesisBiomolecular EngineeringGood Yields
Abstract The first asymmetric intramolecular Stetter reaction is reported, using the chiral triazolium salt 1 as catalyst. Starting from the easily accessible 4‐(2‐formylphenoxy)but‐2‐enoates 2 , this protocol opens up an enantioselective pathway to the benzo‐annulated pyran‐4‐ones (chroman‐4‐ones) 3a–h with good yields and enantiomeric excesses of up to 74%.
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