Skip to main content
placeholder image

The synthesis of a novel carbazole-linked cyclic peptoid with antibacterial activity

Journal Article


Abstract


  • This paper describes the synthesis of a novel cyclic peptoid 11, structurally comprising a tripeptide moiety linked through a carbazole scaffold. In a key step, a ring-closing metathesis reaction was used giving efficient access to a new class of cyclic peptoids.

Publication Date


  • 2002

Citation


  • Bremner, J. B., Coates, J. A., Pyne, S. G., Keller, P. A., & Witchard, H. M. (2002). The synthesis of a novel carbazole-linked cyclic peptoid with antibacterial activity. Synlett, (2), 219-222. doi:10.1055/s-2002-19754

Scopus Eid


  • 2-s2.0-0036166674

Web Of Science Accession Number


Start Page


  • 219

End Page


  • 222

Issue


  • 2

Abstract


  • This paper describes the synthesis of a novel cyclic peptoid 11, structurally comprising a tripeptide moiety linked through a carbazole scaffold. In a key step, a ring-closing metathesis reaction was used giving efficient access to a new class of cyclic peptoids.

Publication Date


  • 2002

Citation


  • Bremner, J. B., Coates, J. A., Pyne, S. G., Keller, P. A., & Witchard, H. M. (2002). The synthesis of a novel carbazole-linked cyclic peptoid with antibacterial activity. Synlett, (2), 219-222. doi:10.1055/s-2002-19754

Scopus Eid


  • 2-s2.0-0036166674

Web Of Science Accession Number


Start Page


  • 219

End Page


  • 222

Issue


  • 2