4.8 Article

Total Synthesis of (±)-Exotine B

Journal

ORGANIC LETTERS
Volume 20, Issue 14, Pages 4358-4361

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.8b01817

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Funding

  1. New York University
  2. National Institutes of Health [OD016343]
  3. German Academic Scholarship Foundation

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The heterodimeric indole/coumarin natural product exotine B was synthesized for the first time. The carbon skeleton of the natural product was formed rapidly by a palladium-catalyzed Suzuki cross-coupling reaction and a gallium-catalyzed three-component [4 + 3] cycloaddition reaction. An alternative biosynthesis of exotine B is proposed based on the total synthesis. Improved syntheses of coumarin natural products gleinadiene and coumurrayin are also reported.

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