The Journal of Organic Chemistry · 2010 · 58 citations · 48 references
Natural SciencesChemistryCatalysisOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisReaction MechanismsRetrosynthetic AnalysisPalladium-catalyzed Cross-couplingQuinoline ChemistryQuinoline SynthesisSonogashira Coupling
A domino reaction via palladium-catalyzed Sonogashira coupling of benzimidoyl chlorides with 1,6-enynes and then cyclization to form quinoline derivatives has been developed. The reaction conditions and the scope of the process are examined, and a plausible mechanism is proposed. The procedure is simple, rapid, and general, and the substrates are readily available.
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Todd Schwier, Anna W. Sromek, Dahrika M. L. Yap et al. · Journal of the American Chemical Society · 2007 · 296 citations · Full text
Norio Sakai, Kimiyoshi Annaka, Akiko Fujita et al. · The Journal of Organic Chemistry · 2008 · 206 citations