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Nickel(ii)-catalyzed C(sp2)-H sulfuration/annulation with elemental sulfur: selective access to benzoisothiazolones
Jun-Ru Guo1, Jun-Fang Gong1, Mao-Ping Song1
1College of Chemistry and Molecular Engineering, Henan Key Laboratory of Chemical Biology and Organic Chemistry, Zhengzhou University, Zhengzhou 450001, People's Republic of China. gongjf@zzu.edu.cn mpsong@zzu.edu.cn.
Abstract:
The first nickel(ii)-catalyzed direct sulfuration/annulation of C(sp2)-H bonds with elemental sulfur has been achieved by using 2-amino alkylbenzimidazole (MBIP-amine) as a N,N-bidentate directing group. This strategy tolerates a wide range of functional groups, furnishing structurally diverse benzoisothiazolone derivatives with benzimidazole skeletons in moderate to excellent yields in a simple and efficient way.
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