RIS ID
16733
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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Publication Details
This article was originally published as: Au, VS, Bremner, JB, Coates, J, et al, Synthesis of some cyclic indolic peptoids as potential antibacterials, Tetrahedron, 2006, 62(40), 9373-9382. The original journal can be found here through Elsevier.