An Oxidative Palladium-Catalyzed Remote meta–Selective Homo-Biaryl-Coupling Assisted by Nitrile Directing Templates

Remote meta-C–H functionalization has emerged as a transformative approach in organic synthesis, allowing the selective functionalization of inactivated meta-C–H bonds. While considerable progress has been made in meta-C–H functionalization strategies, including olefination, cyanation, acetoxylation, and arylation, however, the regioselective meta-C–H homo-biaryl coupling remains unexplored. In this study, we report the first palladium-catalyzed oxidative protocol for regioselective meta-C–H homo-biaryl coupling, targeting substrates such as 3-phenylpropanoic acid, 2-phenylethan-1-ol, phenylacetic acid, and phenylmethane sulfonic acid derivatives. This method significantly enhances the synthetic toolbox for constructing complex biaryl frameworks with exceptional precision. The reaction proceeds efficiently under ambient conditions, with copper trifluoromethanesulfonate identified as a critical additive for driving the process. Furthermore, this strategy has been extended to the synthesis of complex trimeric and diolefination products. The protocol delivered the desired products in good yields with excellent regioselectivity and demonstrated broad applicability across a range of substrates bearing diverse aliphatic and aromatic nitrile-based directing group templates.