4.7 Article

Total Synthesis of Cryptoacetalide

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 75, Issue 15, Pages 5355-5358

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo100867v

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Funding

  1. National Science Foundation [0846756]
  2. Direct For Mathematical & Physical Scien
  3. Division Of Chemistry [0846756] Funding Source: National Science Foundation

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We are reporting the first total synthesis of the tetracyclic terpene natural product cryptoacetalide. Key steps of the synthesis are a microwave-mediated [2+2+2] cyclotrimerization reaction to construct the central benzene ring, and a light-mediated radical cyclization to assemble the spiro-ketal moiety.

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