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Highly enantioselective dynamic kinetic resolution and desymmetrization processes by cyclocondensation of chiral aminoalcohols with racemic or prochiral δ-oxoacid derivatives
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Citations
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References
2005
Year
High EnantioselectivityProchiral Delta-oxoacid DerivativesBioorganic ChemistryEngineeringBiochemistryChiral AminoalcoholsNatural SciencesOrganic ChemistryProchiral δ-Oxoacid DerivativesCyclocondensation ReactionsStereoselective SynthesisChemistryDesymmetrization ProcessesAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringNatural Product Synthesis
Cyclocondensation reactions of aminoalcohols and with racemic or prochiral delta-oxoacid derivatives provide polysubstituted lactams with high enantioselectivity in a process that involves dynamic kinetic resolution and/or desymmetrization of enantiotopic or diastereotopic ester groups.
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