Selective synthesis of fluorinated biaryls by [MCl2(PhPEWO-F)] (M = Ni, Pd) catalysed Negishi cross-coupling†
Abstract
Highly selective cross-couplings to polyfluorinated assymmetric biaryls, including the symmetric biaryl C6F5–C6F5, are achieved at relatively low temperature (80 °C) and in short times using [MCl2(PhPEWO-F)] catalysts (M = Ni, Pd; PhPEWO-F = 1-(PPh2), 2-(CH![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif) CH–C(O)Ph)–C6F4), ArFI, and Zn(C6F5)2 as example of highly fluorinated nucleophile.
CH–C(O)Ph)–C6F4), ArFI, and Zn(C6F5)2 as example of highly fluorinated nucleophile.
- This article is part of the themed collection: Chemical Communications HOT articles
 
                




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