Direct Arylation of Simple Arenes with Aryl Bromides by Synergistic Silver and Palladium Catalysis
Adrián Tlahuext-Aca, Sarah Yunmi Lee, Shu Sakamoto, John F. Hartwig
Abstract
The direct, catalytic arylation of simple arenes in small excess with aryl bromides is disclosed. The developed method does not require the assistance of directing groups and relies on a synergistic catalytic cycle in which phosphine-ligated silver complexes cleave the aryl C-H bond, while palladium catalysts enable the formation of the biaryl products. Mechanistic experiments, including kinetic isotope effects, competition experiments, and hydrogen-deuterium exchange, support a catalytic cycle in which cleavage of the C-H bond by silver is the rate-determining step.
Topics & Concepts
CatalysisChemistryPalladiumArylPhosphineCatalytic cycleCombinatorial chemistryKinetic isotope effectBond cleavageDeuteriumOrganic chemistryPhotochemistryMedicinal chemistryAlkylQuantum mechanicsPhysicsCatalytic C–H Functionalization MethodsCatalytic Cross-Coupling ReactionsRadical Photochemical Reactions