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Synfacts 2025; 21(07): 752
DOI: 10.1055/a-2601-5212
DOI: 10.1055/a-2601-5212
Peptide Chemistry
Synthesis of Fluorinated Analogues of Amino Acids
Iannuzzi M *,
Hohmann T *,
Dyrks M,
Haoues K,
Salamon-Krokosz K,
Koksch B *.
Freie Universität Berlin, Germany
Asymmetric Synthesis of Fluorinated Derivatives of Aromatic and γ-Branched Amino Acids via a Chiral Ni(II) Complex.
Beilstein J. Org. Chem. 2025;
21: 659-669
DOI: 10.3762/bjoc.21.52
Asymmetric Synthesis of Fluorinated Derivatives of Aromatic and γ-Branched Amino Acids via a Chiral Ni(II) Complex.
Beilstein J. Org. Chem. 2025;
21: 659-669
DOI: 10.3762/bjoc.21.52

Significance
Fluorinated amino acids are crucial building blocks in organic synthesis. The authors report here the chiral Ni(II) complex mediated gram-scale synthesis of non-canonical amino acids.
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Comment
This work highlights the remarkable potential of chiral nickel complexes in synthesizing fluorinated amino acids. The ability to generate a diverse array of these compounds from a single starting material is a significant advantage in fluoropeptide chemistry.
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Publication History
Article published online:
23 June 2025
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