Catalytic, One-Pot Synthesis of β-Amino Acids from α-Amino Acids. Preparation of α,β-Peptide Derivatives

The one-pot conversion of readily available α-amino acid into β-amino acid derivatives was carried out in good yields. The method is a sequential process initiated by a tandem radical decarboxylation−oxidation reaction; the resulting acyliminium ion was trapped by silyl ketenes. Stoichiometric and c...

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Veröffentlicht in:Journal of organic chemistry 2009-07, Vol.74 (13), p.4655-4665
Hauptverfasser: Saavedra, Carlos, Hernández, Rosendo, Boto, Alicia, Álvarez, Eleuterio
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Sprache:eng
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Zusammenfassung:The one-pot conversion of readily available α-amino acid into β-amino acid derivatives was carried out in good yields. The method is a sequential process initiated by a tandem radical decarboxylation−oxidation reaction; the resulting acyliminium ion was trapped by silyl ketenes. Stoichiometric and catalytic versions of this reaction were developed and then applied to prepare modified di- and tripeptides. Interestingly, some tripeptides formed expanded β-turns in the solid state.
ISSN:0022-3263
1520-6904
DOI:10.1021/jo9004487