A simple, efficient, and recyclable phosphine-free catalytic system for carbonylative suzuki coupling reaction of aryl and heteroaryl iodides

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47 Scopus citations

Abstract

The carbonylative Suzuki cross-coupling reaction of arylboronic acid with aryl and heteroaryl iodides using polymer supported palladium-N-heterocyclic carbene complex (PS-Pd-NHC) as an efficient heterogeneous, recyclable catalyst is described. The developed catalytic system is found to be effective for the carbonylative coupling reaction of aryl, heteroaryl, and bicyclic heteroaryl iodides (5-iodoindole and 3-iodoquinoline) with various arylboronic acid derivatives providing good to excellent yields of the desired products. The protocol is advantageous due to the ease in handling of the catalyst and simple workup procedure, and environmentally benign with effective catalyst recyclability.

Original languageEnglish
Article numberP15410SS
Pages (from-to)243-250
Number of pages8
JournalSynthesis
Issue number2
DOIs
StatePublished - 2011
Externally publishedYes

Keywords

  • Suzuki carbonylation
  • biaryl ketones
  • boron
  • heterogeneous catalysis
  • palladium

ASJC Scopus subject areas

  • Catalysis
  • Organic Chemistry

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