Synthesis and antibacterial activity of some binaphthyl-supported macrocycles containing a cationic amino acid
RIS ID
42786
Abstract
As part of a programme investigating antibacterial cyclic macrocycles containing a cationic amino acid with an internal aromatic hydrophobic scaffold, we previously reported a macrocycle anchored at the 3,3-positions of a 1,1-binaphthyl unit. This was prepared via key intermediates containing an internal allylglycine and an allyl-substituted binaphthyl unit for a subsequent ring-closing metathesis reaction. This paper presents some structure-activity relationship studies with additional macrocycles based on this lead compound against Staphylococcus aureus together with the antibacterial activity of two related acyclic compounds. C 2011 Elsevier Ltd. All rights reserved.
Publication Details
Coghlan, D. R., Bremner, J. B., Keller, P. A., Pyne, S. G., David, D. M., Somphol, K., Baylis, D., Coates, J., Deadman, J., Rhodes, D. I. & Robertson, A. D. (2011). Synthesis and antibacterial activity of some binaphthyl-supported macrocycles containing a cationic amino acid. Bioorganic and Medicinal Chemistry, 19 (11), 3549-3557.