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      A gold-catalyzed unique cycloisomerization of 1,5-enynes: efficient formation of 1-carboxycyclohexa-1,4-dienes and carboxyarenes.

      1 ,
      Journal of the American Chemical Society
      American Chemical Society (ACS)

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          Abstract

          A novel Au-catalyzed migratory cycloisomerization strategy is advanced. Implementation of this strategy led to the development of a unique Au-catalyzed 1,5-enyne cycloisomerizatioin involving carboxy migration and Au-mediated C-C single bond formation. 1-Carboxycyclohexa-1,4-dienes and carboxyarenes can be prepared with good efficiency and with flexible substitution patterns.

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          Author and article information

          Journal
          J. Am. Chem. Soc.
          Journal of the American Chemical Society
          American Chemical Society (ACS)
          0002-7863
          0002-7863
          Nov 08 2006
          : 128
          : 44
          Affiliations
          [1 ] Department of Chemistry/216, University of Nevada, Reno, 1664 North Virginia Street, Reno, Nevada 89557, USA.
          Article
          10.1021/ja066220f
          17076498
          e0c321b5-9edc-4881-9e01-06d737cd44ed
          History

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