Publication | Closed Access
Synergistic Cu/Pd‐Catalyzed Asymmetric Allenylic Alkylation of Azomethine Ylides for the Construction of α‐Allene‐Substituted Nonproteinogenic α‐Amino Acids
58
Citations
51
References
2019
Year
Available Imine EstersEngineeringAzomethine YlidesNatural SciencesDiversity-oriented SynthesisOrganic ChemistryPeptide Scienceα-Amino AcidCatalysisStereoselective SynthesisChemistrySynergistic Cu/pd CatalysisOrganometallic CatalysisNatural Product SynthesisAsymmetric CatalysisEnantioselective SynthesisBiomolecular Engineering
An unprecedented asymmetric allenylic alkylation of readily available imine esters, which was enabled by a synergistic Cu/Pd catalysis, has been developed. This dual catalytic system possesses good substrate compatibility, delivering a diverse array of nonproteinogenic α-allenylic α-mono- or α,α-disubstituted α-amino acids (α-AAs) with high yields and generally excellent enantioselectivities. Furthermore, the scalability and practicability of the current synthetic protocol were proven by performing gram-scale reactions and by the first catalytic asymmetric synthesis of naturally occurring (S)-γ-allenic α-amino acid, respectively.
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