Journal of the American Chemical Society · 2013 · 338 citations · 39 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryCatalytic MechanismsTarget-oriented SynthesisC - H Bond FunctionalizationCatalytic FunctionalizationElectrophilic Aromatic SubstitutionElectrophilic Substitution In HeterocyclesHeterocycle FunctionalizationMedicinal Chemistry Applications
A combination of weakly coordinating auxiliaries and ligand acceleration allows for the development of both ortho- and meta-selective C-H olefination of phenol derivatives. These reactions demonstrate the feasibility of directing C-H functionalizations when functional groups are distal to target C-H bonds. The meta-C-H functionalization of electron-rich phenol derivatives is unprecedented and orthogonal to previous electrophilic substitution of phenols in terms of regioselectivity. These methods are also applied to functionalize α-phenoxyacetic acids, a fibrate class of drug scaffolds.
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Remarkably Selective Iridium Catalysts for the Elaboration of Aromatic C-H Bonds
Jian-Yang Cho, Man Kin Tse, Daniel Holmes et al. · Science · 2002 · 1.1K citations