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

DOI: 10.1039/CC9960000633

Source and publish data:

Chemical Communications p. 633 - 634 (1996)

Update date:2022-08-04

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Authors:

Palomo, Claudio

Aizpurua, Jesus M.

Galarza, Regina

Mielgo, Antonia

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Article abstract of DOI:10.1039/CC9960000633

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.

Full text of DOI:10.1039/CC9960000633

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