• Title of article

    Reaction of aryl di-, tri-, or tetrabromides with arylboronic acids or alkenes in the presence of a palladium-tetraphosphine catalyst

  • Author/Authors

    Florian Berthiol، نويسنده , , Isabelle Kondolff، نويسنده , , Henri Doucet، نويسنده , , Maurice Santelli، نويسنده ,

  • Issue Information
    دوفصلنامه با شماره پیاپی سال 2004
  • Pages
    13
  • From page
    2786
  • To page
    2798
  • Abstract
    cis,cis,cis -1,2,3,4-Tetrakis(diphenylphosphinomethyl)cyclopentane/View the MathML source12[PdCl(C3H5)]2 system catalyses the Suzuki and Heck reactions of aryl di-, tri-, or tetrabromides with a range of arylboronic acids or alkenes with moderate to high ratio substrate/catalyst in good yields. Aryl polybromides such as dibromobenzenes, 1,3,5-tribromobenzene, 1,2,4,5-tetrabromobenzene, dibromopyridines or a dibromothiophene have been successfully used. Convenient synthesis of a variety of di- and triarylated or vinylated compounds and even a 1,2,4,5-tetraarylated compound were prepared by use of this reaction.
  • Keywords
    Tetraphosphine , Palladium , Suzuki-coupling , Heck-vinylation , arylboronic acids , Alkenes , Aryl bromides
  • Journal title
    Journal of Organometallic Chemistry
  • Serial Year
    2004
  • Journal title
    Journal of Organometallic Chemistry
  • Record number

    1377306