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Asymmetric Synthesis via Heterocyclic Intermediates; XXX<sup>1</sup>. Asymmetric Synthesis of Glutamic Acids and Derivatives thereof by the Bislactim-Ether Method. Michael-Addition of Methyl 2-Alkenoates to the Lithiated Bislactim-Ether of Cyclo-(L-Val- Gly)
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1986
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DerivativesLithiated Bislactim-ether-Glutamic AcidsGlutamic AcidsNatural SciencesEngineeringDiversity-oriented SynthesisAsymmetric SynthesisBis-lactim EtherOrganic ChemistryStereoselective SynthesisChemistryPharmacologyAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringNatural Product Synthesis
An asymmetric synthesis of (virtually configurationally pure) (R)-glutamic acids and/or the corresponding (R)-2-amino-5-pyrrolidinones starting with the bis-lactim ether of cyclo-(L-Val-Gly) and methyl 2-alkenoates is described.