4.8 Article

Total Synthesis of Cladoniamide G

Journal

ORGANIC LETTERS
Volume 15, Issue 5, Pages 1152-1154

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol400055v

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Funding

  1. University of British Columbia
  2. Natural Science and Engineering Research Council (NSERC) of Canada
  3. Canada Foundation for Innovation (CFI)
  4. Canadian Cancer Society Research Institute

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The total synthesis of cladoniamide G, a cytotoxic compound against MCF-7 breast cancer cells (10 mu g/mL), was accomplished. Key steps in the sequence include oxidative dimerization of 3-acetoxy-5-chloroindole and a tandem process incorporating three steps: bimolecular carbonyl addition, lactam formation, and carbamate removal.

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