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      Silver-catalyzed cyclization of α-imino-oxy acids to fused tetralone derivatives

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          Abstract

          A silver-catalyzed cyclization of α-imino-oxy acids under mild conditions has been described. This reaction offers facile access to a diverse range of fused tetralone derivatives with exquisite stereoselectivity in moderate to good yields.

          Abstract

          A silver-catalyzed intramolecular radical relay cyclization of α-imino-oxy acids under mild conditions has been described. This reaction offers facile access to a diverse range of fused tetralone derivatives with exquisite stereoselectivity in moderate to good yields (40–98%). Experimental studies show that the reaction undergoes a decarboxylation and acetone fragmentation/1,5-hydrogen atom transfer (HAT)/cyclization process.

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          Chemistry with Electrochemically Generated N-Centered Radicals

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            Visible Light-Driven Radical-Mediated C–C Bond Cleavage/Functionalization in Organic Synthesis

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              Metal-Catalyzed Decarboxylative C–H Functionalization

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                Author and article information

                Contributors
                Journal
                OBCRAK
                Organic & Biomolecular Chemistry
                Org. Biomol. Chem.
                Royal Society of Chemistry (RSC)
                1477-0520
                1477-0539
                March 29 2023
                2023
                : 21
                : 13
                : 2700-2704
                Affiliations
                [1 ]School of Petrochemical Engineering, Liaoning Petrochemical University, Fushun 113001, China
                [2 ]College of Food Science and Pharmaceutical Engineering, Zaozhuang University, Zaozhuang 277160, China
                [3 ]College of Chemistry and Chemical Engineering, Shangqiu Normal University, Shangqiu 476000, China
                [4 ]School of Chemistry, Beihang University, Beijing, 100191, China
                Article
                10.1039/D2OB02329F
                1b86685d-e4c0-431f-8645-108664edf1ad
                © 2023

                http://rsc.li/journals-terms-of-use

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