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Synfacts 2009(6): 0624-0624
DOI: 10.1055/s-0029-1216665
DOI: 10.1055/s-0029-1216665
Synthesis of Materials and Unnatural Products
© Georg Thieme Verlag
Stuttgart ˙ New York
Fully Fluorinated Pentaphenylborole
C. Feng, W. E. Piers*, M. Parvez
University of Calgary, Canada
Further Information
Publication History
Publication Date:
25 May 2009 (online)
Significance
The authors report a synthesis of perfluorinated pentaphenylborole (2). Perfluorination, along with the antiaromaticity of the borole ring makes 2 a potent Lewis acid and possible precursors to a variety of interesting materials and building blocks.