(2S,4R)- and (2S,4S)‑Perfluoro-tert-butyl 4‑Hydroxyproline: Two Conformationally Distinct Proline Amino Acids for Sensitive Application in 19F NMR

(2S,4R)- and (2S,4S)-Perfluoro-tert-butyl 4-Hydroxyproline: Two ConformationallyDistinct ProlineAmino Acids for Sensitive Application in 19F NMR

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Synthesis of Perfluoro-tert-butyl Tyrosine, for Application in$ ^{19}$F NMR, via a Diazonium-Coupling Reaction

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Perfluoro-tert-butyl Homoserine Is a Helix-Promoting, Highly Fluorinated, NMR-Sensitive Aliphatic Amino Acid: Detection of the Estrogen Receptor·Coactivator Protein–Protein Interaction by$ ^{19}$F NMR

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Electrochemical Decarboxylation of Hydroxyproline: A Simple Three-Step Conversion of (2S,4R)-4-Hydroxyproline to (R)-γ-Amino-β-hydroxybutanoic Acid (GABOB)

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The Implications of (2S,4S)-Hydroxyproline 4-O-Glycosylation for Prolyl Amide Isomerization

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