Bulletin of the Chemical Society of Japan · 1972 · 40 citations · 4 references
Natural SciencesBiochemistryBioorganic ChemistryOrganometallic ChemistryProtein BiochemistryAmino Acid ChemistryPeptide Bond ChemistryPeptide ChemistryAmino Acid AnaloguesAmino Acid DerivativesAmino Acid ReactivityAmino AcidsAmino Protecting GroupsPeptide Coupling ReactionsPeptide Coupling ReagentsReactivity
Abstract The chemical reactivity of α-aminobenzylphosphonic acid was investigated in order to survey the methods for incorporating aminophosphonic acids into a peptide chain. The investigation revealed that i) a dipeptide analog linked with a phosphonamide bond could be produced by the reaction of C-protected amino acid with the N-protected aminophosphonomonochloridate, and that ii) amino groups of the aminophosphonic acid possessed a reactivity similar to those of amino acids, and were capable of coupling with N-protected amino acids by means of dicyclohexylcarbodiimide.
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