Solid-phase peptide synthesis of analogues of the N-terminus A-ring fragment of the lantibiotic nisin: Replacements for the dehydroalanine (Dha) residue at position 5 and the first incorporation of a thioamide residue

Kim Manzor, Keith Proinsias, Fintan Kelleher

Research output: Contribution to journalArticlepeer-review

4 Citations (Scopus)

Abstract

A number of A-ring analogues of the lantibiotic nisin, containing replacements for the Dha residue at position 5, have been successfully prepared by solid-phase peptide synthesis. The Dha replacements include glycine, alanine, phenylalanine, serine and 1-aminocyclopropyl carboxylic acid (ACCa). The incorporation of a thioamide-isoleucine residue at position 4 is also described and represents the first reported preparation of a lantibiotic ring fragment containing a thioamide link.

Original languageEnglish
Pages (from-to)2959-2963
Number of pages5
JournalTetrahedron Letters
Volume58
Issue number30
DOIs
Publication statusPublished - 2017

Keywords

  • Dehydroalanine
  • Lantibiotics
  • Microwave-enhanced solid-phase peptide synthesis
  • Nisin
  • Thioamide

Fingerprint

Dive into the research topics of 'Solid-phase peptide synthesis of analogues of the N-terminus A-ring fragment of the lantibiotic nisin: Replacements for the dehydroalanine (Dha) residue at position 5 and the first incorporation of a thioamide residue'. Together they form a unique fingerprint.

Cite this