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Chiral phosphoric acid catalyzed enantioselective annulation of acyclic enecarbamates to in situ-generated ortho-quinone methides
33
Citations
55
References
2017
Year
Chemical EngineeringAcyclic EnecarbamatesSitu-generated Ortho-quinone MethidesEngineeringNovel OrganocatalystsTrip CatalystOrganic ChemistryAnnulation ReactionCatalysisO-quinone MethidesChemistryChiral Phosphoric AcidStereoselective SynthesisAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
The first organocatalytic asymmetric reaction of acyclic enecarbamates with o-quinone methides is disclosed. BINOL-based phosphoric acid catalysts were found to be suitable for the annulation reaction. With 10 mol% of the TRIP catalyst, high yields as well as excellent diastereo- and enantioselectivities are achieved for a variety of 2,3,4-trisubstituted chroman products.
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