Nickel-catalysed aromatic Finkelstein reaction of aryl and heteroaryl bromides

Chem Commun (Camb). 2012 Apr 25;48(33):3993-5. doi: 10.1039/c2cc30956d. Epub 2012 Mar 16.

Abstract

A fast and efficient nickel-catalysed iodination reaction of aryl and heteroaryl bromides has been developed. The transformation was found to be general for a wide range of substrates and was used for the synthesis of iodo-PK11195, an imaging agent of Alzheimer's disease and iniparib, a compound used in the treatment of breast cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Benzene / chemical synthesis*
  • Benzene / chemistry*
  • Bromine / chemistry*
  • Catalysis
  • Kinetics
  • Microwaves
  • Nickel / chemistry*
  • Tomography, Emission-Computed, Single-Photon

Substances

  • Nickel
  • Benzene
  • Bromine