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An
unprecedented weak coordination promoted dehydrogenative cross-coupling
reaction has been developed by palladium catalysis, which provides
a convenient access to a wide range of 2,2′-difunctional biaryls
from easily accessible substrates. Both HFIP solvent and oxidants
serve as the critical factors in this new reaction. A plausible mechanism
involving Pd(II)/Pd(IV) is proposed. The reaction demonstrates excellent
reactivity, broad functional-group tolerance and high yields
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