Efficient direct 2,2,2-trifluoroethylation of indoles via C-H functionalization

Chem Commun (Camb). 2015 Mar 14;51(21):4488-91. doi: 10.1039/c5cc00519a.

Abstract

A novel highly C3 selective metal free trifluoroethylation of indoles using 2,2,2-trifuoroethyl(mesityl)-iodonium triflate was developed. The methodology enables the introduction of a trifluoroethyl group in a fast and efficient reaction under mild conditions with high functional group tolerance. Beyond the synthetic developments, quantum chemical calculations provide a deeper understanding of the transformation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbon / chemistry
  • Catalysis
  • Hydrocarbons, Fluorinated / chemistry*
  • Hydrogen / chemistry
  • Indoles / chemistry*
  • Kinetics
  • Quantum Theory

Substances

  • 2,2,2-trifluoroethyl iodide
  • Hydrocarbons, Fluorinated
  • Indoles
  • Carbon
  • Hydrogen