Photochemical Synthesis Of 1,4-Dicarbonyl Bifluorene Compounds Via Oxidative Radical Coupling Using Tempo As The Oxygen Atom Donor

A visible-light-induced metal-free synthesis of 1,4-dicarbonyl compounds from alkyne-containing aryl iodides via photochemical C-I bond cleavage, intramolecular cyclization, oxidation, and intermolecular radical coupling sequence is reported. TEMPO was employed as the oxygen atom donor in this transformation. This protocol provided a new strategy for the synthesis of 1,4-dicarbonyl bifluorene compounds.