New "ofloxacin" type antibacterial agents. Incorporation of the spiro cyclopropyl group at N-1
✍ Scribed by Kiely, John S.; Schroeder, Mel C.; Sesnie, Josephine C.
- Book ID
- 127284031
- Publisher
- American Chemical Society
- Year
- 1988
- Tongue
- English
- Weight
- 647 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0022-2623
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## Abstract The 1‐(5‐fluoro‐2‐pyridyl) or 1‐(3‐fluoro‐4‐pyridyl) group was introduced in the syntheses of new pyridonecarboxylic acid antibacterial agents. 1‐(5‐Fluoro‐2‐pyridyl)‐6‐fluoro‐1,4‐dihydro‐7‐(4‐methyl‐1‐piperazinyl)‐4‐oxoquinolone‐3‐carboxylic acid 7b (DW‐116) showed a moderate __in vitr
Synthesis, Pharmacokinetics, and Biological Activity of a Series of New Pyridonecarboxylic Acid Antibacterial Agents Bearing a 5-Fluoro-2-pyridyl Group or a 3-Fluoro-4-pyridyl Group at N-1. -A variety of new quinolones bearing fluorinated pyridyl groups at N1 ( cf. (VIII), (IX); 18 examples) are syn