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      Pd(OAc)(2)-catalyzed Domino reactions of 1-chloro-2-haloarenes and 2-haloaryl tosylates with hindered Grignard reagents via palladium-associated arynes.

      Organic Letters
      Benzene Derivatives, chemistry, Catalysis, Combinatorial Chemistry Techniques, Hydrocarbons, Halogenated, Indicators and Reagents, Molecular Structure, Palladium, Tosyl Compounds

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          Abstract

          The palladium-associated aryne generation strategy and Pd(OAc)(2)-catalyzed annulative Domino reactions of 1-chloro-2-halobenzenes and 2-haloaryl tosylates with hindered Grignard reagents via palladium-associated arynes are described. The palladium-associated aryne generation strategy described here not only allows the high yield, one-step access to potentially useful substituted fluorenes from readily available 1-chloro-2-halobenzenes and 2-haloaryl tosylates, but may also lead to the development of other tandem reactions based on these readily available ortho leaving group bearing haloarenes. [reaction: see text]

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          Author and article information

          Journal
          17048842
          2517585
          10.1021/ol061989i

          Chemistry
          Benzene Derivatives,chemistry,Catalysis,Combinatorial Chemistry Techniques,Hydrocarbons, Halogenated,Indicators and Reagents,Molecular Structure,Palladium,Tosyl Compounds

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