Publication | Open Access
Enantioselective Conjugate Addition of Dialkylzinc Reagents to Cyclic and Acyclic Enones Catalyzed by Chiral Copper Complexes of New Phosphorus Amidites
332
Citations
22
References
1996
Year
Chemical EngineeringEngineeringZinc ReagentOrganic ChemistryOrganometallic CatalysisCatalysisMonodentate Phosphorus AmiditesChemistrySynthetic ChemistryNew Phosphorus AmiditesAsymmetric CatalysisChiral Copper ComplexesOrganozinc ReagentsEnantioselective SynthesisBiomolecular EngineeringDialkylzinc Reagents
Monodentate phosphorus amidites like 1 and Cu(OTf)2 provide access to the first chiral complexes that catalyze the enantioselective conjugate addition of organozinc reagents to cyclic as well as acyclic enones. The ligand-accelerated process affords β-substituted ketones in excellent yields and with high ee values. Functional groups in the zinc reagent are tolerated.
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