4.4 Article

A convenient synthetic approach to bis-functionalised quaterfluorenes

Journal

TETRAHEDRON LETTERS
Volume 45, Issue 28, Pages 5367-5370

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2004.05.074

Keywords

oligofluorenes.; Ni(0) promoted coupling; amines; boronic esters

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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. (C) 2004 Elsevier Ltd. All rights reserved.

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