4.5 Article

Syntheses of Substituted Furans and Pyrroles by Platinum-Catalyzed Cyclizations of Propargylic Oxiranes and Aziridines in Aqueous Media

Journal

SYNTHESIS-STUTTGART
Volume -, Issue 14, Pages 2454-2466

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0029-1216867

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Funding

  1. Japan Society for the Promotion of Science (JSPS)
  2. Program for the Promotion of Basic and Applied Research for Innovations in the Bio-oriented Industry (BRAIN)

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The reactions of propargylic oxiranes and aziridines with a platinum catalyst in aqueous media are described. Furans having a variety of substituents were conveniently synthesized by the platinum-catalyzed reaction of propargylic oxiranes. The reaction in the presence of N-iodosuccinimide afforded the 3-iodo-substituted furan, which was further functionalized to tetrasubstituted furans with high efficiency. Propargylic aziridines were also reacted with the platinum catalyst to produce the corresponding substituted pyrroles in good yields.

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