4.8 Article

Catalytic Friedel-Crafts Reaction of Aminocyclopropanes

Journal

ORGANIC LETTERS
Volume 15, Issue 14, Pages 3738-3741

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol401616a

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Funding

  1. EPFL
  2. SNF [200021_129874]
  3. F. Hoffmann-La Roche, Ltd.
  4. Swiss National Science Foundation (SNF) [200021_129874] Funding Source: Swiss National Science Foundation (SNF)

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A Lewis acid catalyzed Friedel-Crafts reaction between donor-acceptor aminocyclopropanes and indoles and other electron-rich aromatic compounds is reported. Indole alkylation at the C3 position was generally obtained for a broad range of functional groups and substitution patterns. In the case of C3-substituted indoles, C2 alkylation was observed. The reaction gives a rapid access to gamma amino acid derivatives present in numerous bioactive molecules.

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