Abstract
Nitrofuranyl benzimidazoles can be made in one synthetic step from commercially available starting materials. The compounds displayed unexpected antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci with MICs as low as 1 g ml 1. © 2011 Japan Antibiotics Research Association All rights reserved.
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Moraski, G. C., Thanassi, J. A., Podos, S. D., Pucci, M. J., & Miller, M. J. (2011). One-step syntheses of nitrofuranyl benzimidazoles that are active against multidrug-resistant bacteria. Journal of Antibiotics, 64(10), 667–671. https://doi.org/10.1038/ja.2011.67
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