Publication | Closed Access
Catalytic Asymmetric Alkylation of Nucleophiles: Asymmetric Synthesis of α‐Alkylated Amino Acids
159
Citations
40
References
1997
Year
Modified PeptidesEngineeringAmino AcidsOrganic ChemistryPeptide ScienceChemistrySuch Amino AcidsBiochemistryDiversity-oriented SynthesisAsymmetric SynthesisAvailable AzlactonesCatalytic Asymmetric AlkylationCatalysisNatural Product SynthesisAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringNatural SciencesPeptide SynthesisSynthetic Chemistry
The synthesis of modified peptides depends to a large extent on α-alkylated amino acids. Such amino acids can be prepared in a novel asymmetric synthesis with readily available azlactones: the allylic alkylations of a variety of azlactones catalyzed by palladium proceeds with excellent diastereo- and enantioselectivities [Eq. (a)].
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