One-pot synthesis of difluorinated ortho -terphenyls by site-selective suzuki-miyaura reactions of 1,2-dibromo-3,5-difluorobenzene

  • Muhammad Sharif
  • , Sebastian Reimann
  • , Alexander Villinger
  • , Peter Langer*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

The Suzuki-Miyaura reaction of 1,2-dibromo-3,5-difluorobenzene with two equivalents of arylboronic acids gave difluorinated ortho-terphenyls. The reaction with one equivalent of arylboronic acid resulted in site-selective formation of 2-bromo-3,5-difluoro-biphenyls. The one-pot reaction of 1,2-dibromo-3,5-difluorobenzene with two different arylboronic acids afforded difluorinated ortho-terphenyls containing two different terminal aryl groups.

Original languageEnglish
Pages (from-to)913-916
Number of pages4
JournalSynlett
Issue number6
DOIs
StatePublished - 2010
Externally publishedYes

Keywords

  • Catalysis
  • Organofluorine compounds
  • Palladium
  • Site selectivity
  • Suzuki-Miyaura reaction

ASJC Scopus subject areas

  • Organic Chemistry

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