Ligand-Enabled Stereoselective β-C(sp3)—H Fluorination: Synthesis of Unnatural Enantiopure anti-β-Fluoro-α-amino Acids.
2015
The fluorination is performed on α-amino acid derivatives carrying a broad range of β-substituents such as aryl, hetaryl, alkyl, and alkynyl groups endowed with various functional groups.
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