Suzuki-Miyaura reaction of chloroarenes using Pd(PPh3) 4 as catalyst

Thies Thiemann, Yasuko Tanaka, Soleiman Hisaindee, Maitha Kaabi

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)


The reactivity of a number of chloroarenes was investigated and chloro-nitroarenes were found to undergo facile arylation with Pd(PPh 3)4 / [Pd(PPh3)2Cl 2/n.PPh3] as catalyst. Furthermore, 4-chlorobenzaldehyde underwent arylation under the conditions, albeit with a higher catalyst loading.

Original languageEnglish
Pages (from-to)34-38
Number of pages5
JournalJournal of Chemical Research
Issue number1
Publication statusPublished - 2010


  • Nitrochlorobenzenes
  • Suzuki-miyaura cross-coupling
  • Tetrakis(triphenylphosphino)palladium(0)

ASJC Scopus subject areas

  • General Chemistry


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