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Chiral phosphine-catalyzed asymmetric allylic alkylation of 3-substituted benzofuran-2(3H)-ones or oxindoles with Morita–Baylis–Hillman carbonates
42
Citations
48
References
2012
Year
Asymmetric Catalysis3-Substituted Benzofuran-2Cross-coupling ReactionEngineeringMorita–baylis–hillman CarbonatesOrganic ChemistryCatalysisStereoselective SynthesisChemistryMbh Carbonates3-Substituted OxindolesSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
An efficient chiral phosphine-catalyzed asymmetric substitution reaction of MBH carbonates with 3-substituted benzofuran-2(3H)-ones or 3-substituted oxindoles has been described in this context, giving the corresponding allylic alkylation products bearing adjacent quaternary and tertiary stereogenic centers in high yields, moderate diastereoselectivities and high enantioselectivities under mild conditions.
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