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Title: Visible Light Driven and Copper-Catalyzed C(sp3)-H Functionalization of O-Pentafluorobenzoyl Ketone Oximes. Author: Wu D, Cui SS, Bian F, Yu W. Journal: Org Lett; 2021 Aug 06; 23(15):6057-6061. PubMed ID: 34279963. Abstract: The C(sp3)-H functionalization of O-pentafluorobenzoyl ketone oximes was implemented under visible light irradiation with copper complexes as catalysts. The reactions involve iminyl-radical-mediated intramolecular hydrogen atom transfer as the key step, with the iminyl radicals being generated via copper-effected N-O cleavage. The reaction afforded 3,4-dihydro-2H-pyrroles under the conditions of [Cu(DPEphos)(bcp)]PF6 and DABCO, while γ-pentafluorobenzoyloxy ketones were produced predominantly when [Cu(dpp)2]PF6 and InCl3·4H2O were used as catalysts.[Abstract] [Full Text] [Related] [New Search]