α-Amino-β-hydroxy-γ-lactam for Constraining Peptide Ser and Thr Residue Conformation

α-Amino-β-hydroxy-γ-lactam 1 is a peptide mimic in which the Ser/Thr residue ω-, ψ-, and χ-dihedral angle geometry all are constrained by the 5-membered lactam ring. Lactams 1 were made by employing N-(Fmoc)oxiranylglycine 3 as a bis-electrophile in TFE with cat. BzOH to sequentially alkylate and ac...

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Veröffentlicht in:Organic letters 2010-04, Vol.12 (8), p.1652-1655
Hauptverfasser: St-Cyr, Daniel J, Jamieson, Andrew G, Lubell, William D
Format: Artikel
Sprache:eng
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Zusammenfassung:α-Amino-β-hydroxy-γ-lactam 1 is a peptide mimic in which the Ser/Thr residue ω-, ψ-, and χ-dihedral angle geometry all are constrained by the 5-membered lactam ring. Lactams 1 were made by employing N-(Fmoc)oxiranylglycine 3 as a bis-electrophile in TFE with cat. BzOH to sequentially alkylate and acylate a variety of amino acid derivatives in one pot. Solid-phase synthesis of β-hydroxy-γ-lactam 8, an analogue of the IL-1 modulator 101.10, was achieved using this method for studying Ser/Thr geometry.
ISSN:1523-7060
1523-7052
DOI:10.1021/ol1000582