articleTop 1% cited
Potassium <i>t</i> -Butoxide Alone Can Promote the Biaryl Coupling of Electron-Deficient Nitrogen Heterocycles and Haloarenes
Organic Letters · 2008 · Vol. 10(20) · pp. 4673–4676
Shuichi Yanagisawa✉(Japan Science and Technology Agency)Kirika Ueda(Japan Science and Technology Agency)Tadashi Taniguchi(Japan Science and Technology Agency)Kenichiro Itami(Nagoya University)
Abstract
The biaryl coupling of electron-deficient nitrogen heterocycles and haloarenes can be promoted by potassium t-butoxide alone, without the addition of any exogenous transition metal species. Electron-deficient nitrogen heterocycles such as pyridine, pyridazine, pyrimidine, pyrazine, and quinoxaline are arylated with haloarenes. Control experiments support a radical-based mechanism. Taking these findings into account, radical processes may be partially involved in the reported transition-metal-catalyzed arylation reactions employing t-butoxide bases and haloarenes under elevated temperatures or under microwave irradiation.
Catalytic C–H Functionalization MethodsCatalytic Cross-Coupling ReactionsRadical Photochemical ReactionsPyrazineChemistryPyridazineQuinoxalinePyridineNitrogenPyrimidinePotassiumCatalysisOrganic chemistry
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References
Controlled Microwave Heating in Modern Organic Synthesis
Angewandte Chemie International Edition · 2004 · 3,526 citations
Air Stable, Sterically Hindered Ferrocenyl Dialkylphosphines for Palladium-Catalyzed C−C, C−N, and C−O Bond-Forming Cross-Couplings
The Journal of Organic Chemistry · 2002 · 725 citations
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