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Versatile direct Hiyama‐type C−H arylations of benzamides were accomplished with organosiloxanes by chelation‐assisted cobalt catalysis. The C−H arylation featured broad substrate scope, including challenging C(sp 3 )−H activation, the use of γ‐valerolactone as biomass‐derived solvent, and selectively provided the desired biaryls, even when being highly sterically hindered.
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Bu et al. (2018) studied this question.
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