Abstract

We herein illustrate the dual chelation-assisted strategy for a Ru(II)-catalyzed oxidative ortho-C–H/C–H cross-coupling of phenols with (hetero)aromatic amides with the aid of Zn(OTf)2, which enables to rapidly assemble a rich library of 2′-hydroxybiphenyl-2-carboxylic acid derivatives. This protocol features broad substrate scope, excellent functional group tolerance, air as the terminal oxidant, low molar ratio of coupling partners, and scale-up synthesis. Particularly, this methodology is tolerant of more complex natural product derivatives, thus providing an opportunity for late-stage functionalization. This protocol is also used as a key step for the concise synthesis of Palomid 529, a drug in development for the treatment of glioblastoma and neovascular age-related macular degeneration. With a combination of experimental and theoretical methods, we get more insight into the essential issues of strategy determining the reaction process. The stronger coordinating ability of 2-aryloxypyridine and the l...

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