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Title: Photoredox-Catalyzed Alkylarylation of N-Aryl Bicyclobutyl Amides with α-Carbonyl Alkyl Bromides: Access to 3-Spirocyclobutyl Oxindoles. Author: Fan JH, Yuan J, Xia PF, Zhou J, Zhong LJ, Huang PF, Liu Y, Tang KW, Li JH. Journal: Org Lett; 2024 Mar 15; 26(10):2073-2078. PubMed ID: 38446422. Abstract: A visible-light-induced radical alkylarylation of N-aryl bicyclobutyl amides with α-carbonyl alkyl bromides for the synthesis of functionalized 3-spirocyclobutyl oxindoles is described in which β-selective radical addition of the alkyl radical to N-aryl bicyclobutyl amides forms a key radical intermediate followed by interception with intrinsic arene functional group. This approach can be applicable to a wide range of α-carbonyl alkyl bromides, including primary, secondary, and tertiary α-bromoalkyl esters, ketones, nitriles, and nitro compounds.[Abstract] [Full Text] [Related] [New Search]