Publication | Closed Access
Transition-Metal-Free, Visible-Light-Enabled Decarboxylative Borylation of Aryl <i>N</i>-Hydroxyphthalimide Esters
339
Citations
52
References
2017
Year
Chemical EngineeringFunctional Group ToleranceEngineeringPhotochemistryAryl Radical PrecursorsSupramolecular PolymerSynthetic PhotochemistryOrganic ChemistryOrganometallic CatalysisCatalysisSynthetic ChemistryChemistryPolymer ReactionNovel Borylation ReactionVisible-light-enabled Decarboxylative Borylation
Herein, we report a conceptually novel borylation reaction proceeding via a mild photoinduced decarboxylation of redox-activated aromatic carboxylic acids. This work constitutes the first application of cheap and easily prepared N-hydroxyphthalimide esters as aryl radical precursors and does not require the use of expensive transition metals or ligands. The reaction is operationally simple, scalable, and displays broad scope and functional group tolerance.
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