Ruthenium-Catalyzed C–H Arylation of Diverse Aryl Carboxylic Acids with Aryl and Heteroaryl Halides

Published on 2017-10-13T08:13:47Z (GMT) by
Ruthenium ligated to tricyclohexylphosphine or di-<i>tert</i>-butylbipyridine catalyzes the arylation of carboxylic acids with diverse aryl halides (iodide, bromide, and triflate; aryl and heteroaryl). In addition, arylations with 2-iodophenol formed benzochromenones, carboxylate was shown to be a stronger donor than an amide, and the arylation of a pyridine carboxylate was demonstrated. Stoichiometric studies demonstrated that the added ligand is required for reaction with the electrophile but not the C–H bond.

Cite this collection

Huang, Liangbin; Weix, Daniel J. (2017): Ruthenium-Catalyzed C–H Arylation of Diverse

Aryl Carboxylic Acids with Aryl and Heteroaryl Halides. ACS Publications.