Publication | Closed Access
A Stereoselective Route to Hydroxyethylamine Dipeptide Isosteres
23
Citations
7
References
2000
Year
Syn-selective Grignard AdditionEngineeringOrganic ChemistryHydroxyethylamine Dipeptide IsosteresStereodefined Hydroxyethylamine DipeptideEfficient SynthesisChemistryStereoselective SynthesisAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
An efficient synthesis of stereodefined hydroxyethylamine dipeptide isosteres has been developed, utilizing a syn-selective Grignard addition and reductive amination as the key reactions.
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