Organic Letters · 2020 · 13 citations · 63 references
Asymmetric CatalysisRadical ProcessCross-coupling ReactionEngineeringAlkene MetathesisNatural SciencesDiversity-oriented SynthesisAlkylation ReagentOrganic ChemistryOrganometallic CatalysisCatalysisChemistryCyclic EthersEnantioselective SynthesisBiomolecular Engineering
A meta-dehydrogenative alkylation of arenes with cyclic ethers, ketones, and esters catalyzed by ruthenium is achieved in the presence of a di-tert-butyl peroxide (DTBP) oxidant. Interestingly, when quinoline and isoquinoline are employed as the directing group, or a chain ether as alkylation reagent, the system produces Minisci reaction products. Mechanistic study indicates that meta-dehydrogenative alkylation is a radical process initiated by DTBP with the assistance of a CAr–Ru bond ortho/para-directing effect.
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