The Journal of Organic Chemistry · 2011 · 45 citations · 33 references
Natural SciencesChemistryMedicinal ChemistryOrganic ChemistryHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsOrganic SynthesisParallel SynthesisRetrosynthetic AnalysisBromine ChemistryParallel Synthesis MethodologyParallel Synthesis Of HeterocyclesQuinoline SynthesisRing-forming Reactions
A general approach to 3-fluoro-, 3-chloro-, and 3-bromoquinolines which relies on organosilane-promoted Friedländer reaction of α-haloketones is described. The scope of the methylene component as well as influence of the organosilane component on the outcome of the reaction is studied. The method can be used under parallel synthesis conditions.
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Samson A. Jenekhe, Liangde Lu, Maksudul M. Alam · Macromolecules · 2001 · 772 citations
Natural Sciences, Chemistry, Physics +17
Synthesis and Antibacterial Evaluation of Certain Quinolone Derivatives
Yeh‐Long Chen, Kuo‐Chang Fang, Shu‐Lin Hsu et al. · Journal of Medicinal Chemistry · 2001 · 550 citations
G. ROMA, Mario Di Braccio, Giancarlo Grossi et al. · European Journal of Medicinal Chemistry · 2000 · 440 citations