| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1377710 | Bioorganic & Medicinal Chemistry Letters | 2006 | 6 Pages |
Abstract
A series of pyrrolopyridine-substituted oxazolidinones containing various C-5 acetamide isosteres was synthesized and the structure–antibacterial activity relationships determined against a representative panel of susceptible and resistant Gram-positive bacteria.
Graphical abstractA series of pyrrolopyridine-substituted oxazolidinones containing various C-5 acetamide isosteres was synthesized and the structure–antibacterial activity relationships determined against a representative panel of susceptible and resistant Gram-positive bacteria.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Steven D. Paget, Christine M. Boggs, Barbara D. Foleno, Raul M. Goldschmidt, Dennis J. Hlasta, Michele A. Weidner-Wells, Harvey M. Werblood, Karen Bush, Mark J. Macielag,