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      Diversity-Oriented Synthesis of 13- to 18-Membered Macrolactams via Ring-Closing Metathesis

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      The Journal of Organic Chemistry
      American Chemical Society (ACS)

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          Abstract

          An efficient build/couple/pair approach to diversity-oriented synthesis was employed to access several structurally complex macrolactams. In this paper, we describe the successful evaluation of ring-closing metathesis toward the systematic generation of skeletal diversity. By appropriately varying the nature and chain length of the alkenol fragment, a diverse collection of 13- to 18-membered macrolactams were obtained.

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          Author and article information

          Journal
          The Journal of Organic Chemistry
          J. Org. Chem.
          American Chemical Society (ACS)
          0022-3263
          1520-6904
          October 07 2011
          October 07 2011
          : 76
          : 19
          : 8042-8048
          Article
          10.1021/jo2011957
          4284946
          21875084
          dee101aa-d1da-43f8-a4d3-6b0291d18718
          © 2011
          History

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