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Sulfonate Versus Sulfonate: Nickel and Palladium Multimetallic Cross-Electrophile Coupling of Aryl Triflates with Aryl Tosylates

Kai Kang, Liangbin Huang, Daniel J. Weix

2020Journal of the American Chemical Society121 citationsDOIOpen Access PDF

Abstract

While phenols are frequent and convenient aryl sources in cross-coupling, typically as sulfonate esters, the direct cross-Ullmann coupling of two different sulfonate esters is unknown. We report here a general solution to this challenge catalyzed by a combination of Ni and Pd with Zn reductant and LiBr as an additive. The reaction has broad scope, as demonstrated in 33 examples (65% ± 11% average yield). Mechanistic studies show that Pd strongly prefers the aryl triflate, the Ni catalyst has a small preference for the aryl tosylate, aryl transfer between catalysts is mediated by Zn, and Pd improves yields by consuming arylzinc intermediates.

Topics & Concepts

SulfonateArylChemistryTrifluoromethanesulfonateElectrophilePalladiumCatalysisNickelPhenolsOrganic chemistryMedicinal chemistryCombinatorial chemistrySodiumAlkylCatalytic Cross-Coupling ReactionsCatalytic C–H Functionalization MethodsOrganoboron and organosilicon chemistry
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