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Light-Mediated Asymmetric Aliphatic C–H Alkylation with Hydrogen Atom Transfer Catalyst and Chiral Phosphoric Acid
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Citations
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References
2020
Year
Chemical EngineeringAllylic HydrocarbonsEngineeringPhotoredox ProcessPhotochemistryUnactivated HydrocarbonsSynthetic PhotochemistryOrganic ChemistryCatalysisChemistryChiral Phosphoric AcidAsymmetric CatalysisExocyclic EnonesEnantioselective Synthesis
In the presence of tetrabutylammonium decatungstate and chiral spiro phosphoric acid, a light-mediated asymmetric C–H functionalization of unactivated hydrocarbons with exocyclic enones has been established. A wide range of cycloalkanes, benzylic, and allylic hydrocarbons are tolerated. This protocol proceeds via a hydrogen atom transfer/radical addition/hydrogen abstraction/enantioselective protonation relay process.
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