Three-component ruthenium-catalyzed remote C–H functionalization of 8-aminoquinoline amides

Surface Modification Component (thermodynamics)
DOI: 10.1039/d0cc05491g Publication Date: 2020-09-16T16:18:59Z
ABSTRACT
Multicomponent reactions can efficiently construct complex molecular structures from simple precursors. Herein, a novel ruthenium-catalyzed three-component highly selective remote C-H functionalization of 8-aminoquinoline amides has been described. The reaction tolerates wide range functional groups, producing arylation/difluoroalkylation products olefins with potential biological activity and pharmaceutical value. Radical scavenging radical clock experiments show that free process is involved H/D exchange experiment suggests the might involve ortho-C-H activation aromatic ring. A possible mechanism proposed.
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