| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5225723 | Tetrahedron | 2006 | 10 Pages |
Abstract
The synthesis of cyclic peptoids containing an indole hydrophobic scaffold has been realised through the ring-closing metathesis of diallylated precursors. The precursors and their cyclic counterparts possessed poor antibacterial activity in contrast to previously reported cyclic peptoids containing hydrophobic scaffolds.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Vicki S. Au, John B. Bremner, Jonathan Coates, Paul A. Keller, Stephen G. Pyne,