Litcius/Paper detail

Dual ligand-promoted palladium-catalyzed nondirected C–H alkenylation of aryl ethers

Biao Yin, Manlin Fu, Lei Wang, Jiang Liu, Qing Zhu

2020Chemical Communications38 citationsDOI

Abstract

Direct C-H functionalization of aryl ethers remains challenging owing to their low reactivity and selectivity. Herein, a novel strategy for nondirected C-H alkenylation of aryl ethers promoted by a dual ligand catalyst was demonstrated. This catalytic system readily achieved the highly efficient alkenylation of alkyl aryl ethers (anisole, phenetole, n-propyl phenyl ether, n-butyl phenyl ether and benzyl phenyl ether), cyclic aryl ethers (1,4-benzodioxan, 2,3-dihydrobenzofuran, dibenzofuran), and diphenyl oxides. Moreover, the proposed methodology was successfully employed for the late-stage modification of complex drugs containing the aryl ether motif. Interestingly, the compounds developed herein displayed fluorescent properties, which would facilitate their biological applications.

Topics & Concepts

ArylEtherChemistryCatalysisAnisoleDibenzofuranLigand (biochemistry)PalladiumCombinatorial chemistryDiphenyl etherReactivity (psychology)AlkylOrganic chemistryReceptorMedicineBiochemistryAlternative medicinePathologyCatalytic C–H Functionalization MethodsSulfur-Based Synthesis TechniquesCatalytic Cross-Coupling Reactions
Dual ligand-promoted palladium-catalyzed nondirected C–H alkenylation of aryl ethers | Litcius