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Tertiary‐Alcohol‐Directed Functionalization of Remote C(sp<sup>3</sup>)−H Bonds by Sequential Hydrogen Atom and Heteroaryl Migrations
47
Citations
49
References
2017
Year
Remote CEngineeringSynthetic PhotochemistryOrganic ChemistryChemistrySequential Hydrogen AtomHeteroaryl MigrationsOrganometallic CatalysisVisible‐light PhotocatalysisCross-coupling ReactionPhotochemistryChemical BondDiversity-oriented SynthesisCatalysisQuantum ChemistryMolecular ChemistryBiomolecular EngineeringNatural SciencesHydrogen BondRemote Hydrogen Atom
Abstract Reported for the first time is a tertiary‐alcohol‐guided heteroarylation of remote C(sp 3 )−H bonds. The mild and direct generation of alkoxyl radicals from alcohols is enabled by visible‐light photocatalysis. A remote hydrogen atom and heteroaryl migration sequence are involved in the reaction. Many sensitive groups remain intact in the reaction, thus illustrating wide functional‐group compatibility. This protocol provides a practical strategy for the late‐stage modification of alkyl ketones.
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