Issue 5, 1996

A new and versatile procedure for the incorporation of α,β-diamino acids into peptides

Abstract

A new route to peptide segments incorporating α,β-diamino acids either at the α- or β-positions is provided by enzymeimimetic ring opening of 3-amino β-lactams with α-amino acid esters promoted by sodium azide or potassium cyanide.

Article information

Article type
Paper

Chem. Commun., 1996, 633-634

A new and versatile procedure for the incorporation of α,β-diamino acids into peptides

C. Palomo, J. M. Aizpurua, R. Galarza and A. Mielgo, Chem. Commun., 1996, 633 DOI: 10.1039/CC9960000633

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