Publication | Closed Access
Synthesis of Unnatural α-Amino Acids via Photoinduced Decatungstate-Catalyzed Giese Reactions of Aldehydes
61
Citations
35
References
2021
Year
Robust MethodBiosynthesisBioorganic ChemistryEngineeringBiochemistryPhotochemistryNatural SciencesDiversity-oriented SynthesisUnnatural Amino AcidsOrganic ChemistryCatalysisChemistryNatural Product SynthesisSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringSeveral Amino AcidUnnatural α-Amino Acids
Synthesis of unnatural amino acids has long been a focus of chemistry research. Here, we present an efficient, general method that furnishes γ-carbonyl α-amino acids via photoinduced decatungstate-catalyzed Giese reactions of readily available aldehydes as radical precursors. This mild, robust method is compatible with a wide array of functional groups and has a broad substrate scope. We demonstrated the utility of the method by modifying several amino acid bearing drugs and natural products.
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