Publication | Closed Access
A General Amino Acid Synthesis Enabled by Innate Radical Cross‐Coupling
135
Citations
58
References
2018
Year
Molecular BiologyOrganic ChemistryPeptide ScienceProtein SynthesisMedicinal ChemistryDirect UnionPure α‐Amino AcidsStereoselective SynthesisBiochemistryInnate Radical Cross‐couplingRadical (Chemistry)Diversity-oriented SynthesisExotic α‐Amino AcidsPharmacologyAsymmetric CatalysisEnantioselective SynthesisNatural SciencesMedicineDrug Discovery
Abstract The direct union of primary, secondary, and tertiary carboxylic acids with a chiral glyoxylate‐derived sulfinimine provides rapid access into a variety of enantiomerically pure α‐amino acids (>85 examples). Characterized by operational simplicity, this radical‐based reaction enables the modular assembly of exotic α‐amino acids, including both unprecedented structures and those of established industrial value. The described method performs well in high‐throughput library synthesis, and has already been implemented in three distinct medicinal chemistry campaigns.
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