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Ligand-Controlled Ni(0)–Al(III) Bimetal-Catalyzed C3–H Alkenylation of 2-Pyridones by Reversing Conventional Selectivity

Ge Yin, Yue Li, Rong-Hua Wang, Jiang‐Fei Li, Xue-Tao Xu, Yu‐Xin Luan, Mengchun Ye

2021ACS Catalysis56 citationsDOI

Abstract

Conventional C–H alkenylation with alkynes via low-valent transition-metal catalysis occurs at the C6 or C4 position of 2-pyridone with electron-deficient C–H bonds. A bifunctional ligand-bonded Ni–Al bimetallic catalyst resulted in a reversed selectivity, providing a series of C3-alkenylated 2-pyridones in up to 99% yields.

Topics & Concepts

Bimetallic stripBimetalBifunctionalCatalysisSelectivityLigand (biochemistry)ChemistryTransition metalReversingCombinatorial chemistryMetalOrganic chemistryMaterials scienceReceptorPhysical chemistryBiochemistryComposite materialCatalytic C–H Functionalization MethodsCatalytic Alkyne ReactionsCyclopropane Reaction Mechanisms
Ligand-Controlled Ni(0)–Al(III) Bimetal-Catalyzed C3–H Alkenylation of 2-Pyridones by Reversing Conventional Selectivity | Litcius