A new and versatile procedure for the incorporation of α,β-diamino acids into peptides
- 1 January 1996
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- No. 5,p. 633-634
- https://doi.org/10.1039/cc9960000633
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.Keywords
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