4.8 Article

Indoles Synthesized from Amines via Copper Catalysis

Journal

ORGANIC LETTERS
Volume 15, Issue 7, Pages 1666-1669

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol400444g

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Funding

  1. Welch Foundation [E-1744]
  2. ACS Organic Division (SURF fellowship)
  3. University of Houston

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N-Substituted indoles are synthesized from primary amines through a tandem reaction sequence. Initial condensation of the amine with an alpha-(o-haloaryl)ketone or aldehyde is followed by intramolecular aryl amination catalyzed by CuI. A variety of anilines and alkyl amines, including those with significant steric demands, are converted to indoles in high yields and with varying indole substitution.

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