4.7 Article

Synthesis of Heteroarylated Polyfluorobiphenyls via Palladium-Catalyzed Sequential sp2 C-H Bonds Functionalizations

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JOURNAL OF ORGANIC CHEMISTRY
卷 78, 期 8, 页码 4177-4183

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AMER CHEMICAL SOC
DOI: 10.1021/jo400221x

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  1. Chinese Scholarship Council
  2. Fondation Rennesl
  3. CNRS
  4. Rennes Metropole

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The higher reactivity of C5-H bonds of heteroarenes as compared to C-H bonds of bromopolyfluorobenzenes for palladium-catalyzed direct arylation allows the selective synthesis of the polyfluoroaryl-heteroarenes in moderate to high yields, without C-H bond functionalization of the polyfluorobenzene ring. In most cases, low loading of Pd(OAc)(2) catalyst (0.5-1 mol %) was employed. Then, from these heteroarylated polyfluorobenzenes, the palladium-catalyzed C-H bond functionalization of the polyfluorobenzene ring allows the synthesis of heteroarylated polyfluorobiphenyls.

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