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
Link To Document :
بازگشت