4.7 Article

Palladium catalyzed synthesis of 2-trifluoromethylquinolines through a domino Sonogashira-alkyne carbocyclization process

Journal

CHEMICAL COMMUNICATIONS
Volume 46, Issue 12, Pages 2145-2147

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b925285a

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Funding

  1. National Science Foundation of China [20532040, 20772145]

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A new, rapid and high-yielding method to prepare 3,4-disubstituted 2-trifluoromethylquinolines by a palladium catalyzed tandem Sonogashira-alkyne carbocyclization of beta-trifluoromethyl beta-enaminoketones with arynes is described. Moderate to excellent yields have been achieved under mild conditions. This reaction can also be expanded to the non-fluorine containing substrates. The reaction mechanism is also discussed.

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