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Nickel-Catalyzed Site-Selective C3–H Functionalization of Quinolines with Electrophilic Reagents at Room Temperature

Xinghao Sheng, Mingpan Yan, Bo Zhang, Wai‐Yeung Wong, Nobuaki Kambe, Renhua Qiu

2023ACS Catalysis18 citationsDOIOpen Access PDF

Abstract

Herein, we disclose a mild and versatile nickel-catalyzed method for exclusive C3-selective thioetherification, alkylation, arylation, acylation, and phosphorylation of quinolines with a variety of electrophiles. Unactivated quinolines can be functionalized without directing groups at room temperature. Control experiments indicated that quinolines underwent 1,4-addition with nickel hydride species generated from β-H elimination of alkyl nickel intermediates to produce 1,4-dihydroquinolines, which further went through subsequent nucleophilic attack to external electrophiles and oxidative aromatization to generate C3–H-functionalized products.

Topics & Concepts

ElectrophileChemistryAlkylationNucleophileAcylationCatalysisReagentCombinatorial chemistryAromatizationNickelHydrideDehydrogenationSurface modificationAlkylOrganic chemistryMetalPhysical chemistryCatalytic C–H Functionalization MethodsSulfur-Based Synthesis TechniquesCyclopropane Reaction Mechanisms
Nickel-Catalyzed Site-Selective C3–H Functionalization of Quinolines with Electrophilic Reagents at Room Temperature | Litcius