Abstract
The oxazolidinone class of antimicrobials represents a promising advance in the fight against resistant Gram-positive bacterial infections. Four novel oxazolidinone antimicrobial compounds, each containing a benzodioxin ring system, have been prepared. The general synthesis of each compound begins with the construction of a benzodioxin ring system containing a nitro substituent that ultimately becomes the nitrogen of the oxazolidinone ring. Three of the compounds utilize high yielding 'click chemistry' in their final step. The antimicrobial activities of the new oxazolidinones have been measured and the MIC against Staphylococcus aureus for one of the antimicrobials was determined to be 2-3 μg/mL, which is comparable to the well-known oxazolidinone, linezolid. © 2007 Elsevier Ltd. All rights reserved.
Author supplied keywords
Cite
CITATION STYLE
Ebner, D. C., Culhane, J. C., Winkelman, T. N., Haustein, M. D., Ditty, J. L., & Ippoliti, J. T. (2008). Synthesis of novel oxazolidinone antimicrobial agents. Bioorganic and Medicinal Chemistry, 16(5), 2651–2656. https://doi.org/10.1016/j.bmc.2007.11.040
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.