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

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

Digital Object Identifier (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.

UOW Authors

•   Bremner, John
•   Keller, Paul
•   Pyne, Stephen

Publication Date

• 2002

Publisher

• Georg Thieme Verlag KG 

Published In

• Synlett  Journal

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

Digital Object Identifier (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