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      Visible-light-initiated 4CzIPN catalyzed multi-component tandem reactions to assemble sulfonated quinoxalin-2(1H)-ones

      , , , , , ,
      Chinese Chemical Letters
      Elsevier BV

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          Visible light photoredox-controlled reactions of N-radicals and radical ions

          Radicals are an important class of versatile and highly reactive species. Radicals are an important class of versatile and highly reactive species. Compared with the wide applications of various C-centred radicals, however, the N-radical species including N-centred radicals and radical ions remain largely unexplored due to the lack of convenient methods for their generation. In recent years, visible light photoredox catalysis has emerged as a powerful platform for the generation of various N-radical species and methodology development towards the synthesis of diverse N-containing compounds. In this tutorial review, we highlight recent advances in this rapidly developing area with particular emphases put on the working models and new reaction design.
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            Visible Light-Driven Radical-Mediated C–C Bond Cleavage/Functionalization in Organic Synthesis

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              Recent advances of 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene (4CzIPN) in photocatalytic transformations

              In this review, the recent advances of the application of 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene (4CzIPN) as a photoredox catalyst in the past three years (2016–2018) for various organic reactions are summarized. 1,2,3,5-Tetrakis(carbazol-9-yl)-4,6-dicyanobenzene (4CzIPN) is a typical donor–acceptor fluorophore, with carbazolyl as an electron donor and dicyanobenzene as an electron acceptor. It has emerged as a powerful organophotocatalyst since 2016. Excellent redox window, good chemical stability and broad applicability make 4CzIPN an attractive metal-free photocatalyst. In this review, the recent advances of the application of 4CzIPN as a photoredox catalyst in the past three years (2016–2018) for various organic reactions are summarized.
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                Author and article information

                Journal
                Chinese Chemical Letters
                Chinese Chemical Letters
                Elsevier BV
                10018417
                March 2022
                March 2022
                : 33
                : 3
                : 1479-1482
                Article
                10.1016/j.cclet.2021.08.036
                cc7ad03d-1f13-43b8-9f85-da683d8f33cb
                © 2022

                https://www.elsevier.com/tdm/userlicense/1.0/

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