Title of article :
A convenient synthetic approach to bis-functionalised quaterfluorenes
Author/Authors :
Grisorio، نويسنده , , Roberto and Mastrorilli، نويسنده , , Piero and Nobile، نويسنده , , Cosimo Francesco and Romanazzi، نويسنده , , Giuseppe and Suranna، نويسنده , , Gian Paolo and Meijer، نويسنده , , E.W، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2004
Pages :
4
From page :
5367
To page :
5370
Abstract :
Ni(COD)2 promoted coupling of bromofluorenes functionalised with boronic esters or trimethylsilyl groups proves to be an efficient method for the preparation of reactive bifluorenes, which are key intermediates for the synthesis of bis-substituted oligofluorenes. The synthetic method has been exploited as a key step for the synthesis of a chiral 2,7‴-diiodo-quaterfluorene and a 2,7‴-bis-amino quaterfluorene.
Keywords :
boronic esters , Ni(0) promoted coupling , Oligofluorenes , Amines
Journal title :
Tetrahedron Letters
Serial Year :
2004
Journal title :
Tetrahedron Letters
Record number :
1842349
Link To Document :
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