4.8 Article

Room-Temperature and Transition-Metal-Free Intramolecular α-Arylation of Ketones: A Mild Access to Tetracyclic Indoles and 7-Azaindoles

Journal

ORGANIC LETTERS
Volume 21, Issue 1, Pages 320-324

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.8b03831

Keywords

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Funding

  1. FONCYT
  2. CONICET
  3. SeCyT
  4. ECOS-MINCyT [A15E02]
  5. CNRS-CONICET [248434]
  6. MESR
  7. CNRS
  8. Universite Claude Bernard Lyon 1

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A novel approach for the synthesis of tetracyclic indoles and 7-azaindoles is reported. The strategy involves four steps, with a fast rt intramolecular alpha-arylation of ketones as key step. The reaction was inspected synthetically to achieve the synthesis of 11 novel tetracyclic structures with moderate to very good yields (39-85%). Theoretical combined with experimental studies led us to propose a probable polar mechanism (concerted SNAr).

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