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Synthesis of Fmoc-protected aza-β-amino acids via reductive amination of glyoxylic acid
Authors:Olivier Busnel
Affiliation:Groupe ‘Ciblage et Auto-Assemblages Fonctionnels’, UMR 6510 CNRS, Institut de Chimie, Université de Rennes I, 263 Av. du Général Leclerc, F-35042 Rennes Cedex, France
Abstract:The reductive amination of glyoxylic acid, with a protected Fmoc hydrazine, has been developed as a simple and efficient method for the preparation of Fmoc-aza-β3-amino acid residues (aza-β3-aa). Anchoring on resin of these residues will be described as well as the synthesis of hybrid peptide.
Keywords:Aza-β3-amino acid   Fmoc protecting group   Peptidomimetics   Loading resin   Reductive amination
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