Ionic Liquid Acceleration of Solid-Phase Suzuki−Miyaura Cross-Coupling Reactions

Jefferson D. Revell and A. Ganesan*
Combinatorial Centre of Excellence, Department of Chemistry, University of Southampton, Southampton SO17 1BJ, United Kingdom
Org. Lett., 2002, 4 (18), pp 3071–3073
DOI: 10.1021/ol0263292
Publication Date (Web): August 9, 2002
Copyright © 2002 American Chemical Society
*

In papers with more than one author, the asterisk indicates the name of the author to whom inquiries about the paper should be addressed.

, ganesan@soton.ac.uk

Abstract

Abstract Image

Room-temperature ionic liquids promote various transition metal-catalyzed reactions in the solution phase. Here, for the first time, we show that these effects are translatable to solid-phase reactions. The Suzuki−Miyaura cross-coupling of 4-iodophenol immobilized on polystyrene−Wang resin with various arylboronic acids was significantly accelerated by the ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim][BF4-]).

Tools

History

  • Published In Issue September 05, 2002
  • Received June 8, 2002

Recommend & Share

Related Content

Other ACS content by these authors: