Cascade fluorofunctionalisation of 2,3-unsubstituted indoles by means of electrophilic fluorination

Chem Commun (Camb). 2013 Nov 21;49(90):10602-4. doi: 10.1039/c3cc46564k.

Abstract

Cascade fluorofunctionalisation of 2,3-unsubstituted indoles featuring the formation of C-C, C-F and C-O bonds via electrophilic fluorination using N-fluorobenzenesulfonimide is described. The use of an O-nucleophile tethered to the nitrogen of indoles enables the synthesis of polycyclic fluorinated indoline derivatives from simple precursors in 40-63% yields.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbon / chemistry
  • Cyclization
  • Fluorine / chemistry
  • Halogenation
  • Indoles / chemistry*
  • Oxygen / chemistry
  • Sulfonamides / chemistry
  • Temperature

Substances

  • Indoles
  • Sulfonamides
  • Fluorine
  • N-fluorobenzenesulfonimide
  • indoline
  • Carbon
  • Oxygen