Cobalt-Catalyzed Biaryl
Couplings via C–F Bond
Activation in the Absence of Phosphine or NHC Ligands
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Abstract
A highly general
and selective Co-catalyzed biaryl coupling through
C–F cleavage under phosphine or NHC-free conditions was described.
A broad range of aryl fluorides including unactivated fluorides as
well as those with sensitive functionalities could couple with various
Ti(OEt)<sub>4</sub>-mediated aryl Grignard reagents with high selectivity
under the catalysis of CoCl<sub>2</sub>/DMPU. Importantly, selective
C–F bond activation couplings between two types of fluorines
(difluorinated aromatics and on two different coupling partners) and
in the presence of C–Cl or C–Br bonds could also be
achieved