4.8 Article

Total Synthesis of Benzofuran-Based Aspergillusene B via Halogenative Aromatization of Enones

Journal

ORGANIC LETTERS
Volume 22, Issue 11, Pages 4196-4200

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.0c01259

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Funding

  1. UIC Department of Chemistry
  2. National Science Foundation (CAREER Award) [1654490]
  3. UIC Chancellors Undergraduate Research Award
  4. Division Of Chemistry
  5. Direct For Mathematical & Physical Scien [1654490] Funding Source: National Science Foundation

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A novel non-aromatic pool synthetic strategy for the synthesis of benzofuran-based natural products via oxidative haloaromatization of enones is reported. This approach is successfully applied in the first total synthesis of the natural product aspergillusene B. In comparison with a separately executed aromatic pool synthesis, the non-aromatic pool protocol demonstrates equivalent efficiency but offers a much higher degree of modularity.

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