Ethyl 1,4-Dihydro-4-oxo-1,8-naphthyridine-3-carboxylates by a Tandem SNAr-Addition-Elimination Reaction
Author:
Affiliation:
1. Department of Chemistry; Oklahoma State University; Stillwater Oklahoma 74078-3071
Publisher
Wiley
Subject
Organic Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jhet.917/fullpdf
Reference27 articles.
1. Ethyl 1,4-dihydro-4-oxo-3-quinolinecarboxylates by a tandem addition-elimination-SNAr reaction
2. Synthesis and structure-activity relationships of new arylfluoronaphthyridine antibacterial agents
3. Pyridonecarboxylic acids as antibacterial agents. 9. Synthesis and antibacterial activity of 1-substituted 6-fluoro-1,4-dihydro-4-oxo-7-(4-pyridyl)-1,8-naphthyridine-3-carboxylic acids
4. Design, synthesis, and properties of (4S)-7-(4-amino-2-substituted-pyrrolidin-1-yl)quinolone-3-carboxylic acids
5. Preparation and in vitro and in vivo evaluation of quinolones with selective activity against Gram-positive organisms
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