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      Metal-Catalyzed Reactions of Organoboronic Acids and Esters

      Bulletin of the Chemical Society of Japan
      The Chemical Society of Japan

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          Palladium-Catalyzed Coupling Reactions of Aryl Chlorides

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            Remarkably selective iridium catalysts for the elaboration of aromatic C-H bonds.

            Arylboron compounds have intriguing properties and are important building blocks for chemical synthesis. A family of Ir catalysts now enables the direct synthesis of arylboron compounds from aromatic hydrocarbons and boranes under "solventless" conditions. The Ir catalysts are highly selective for C-H activation and do not interfere with subsequent in situ transformations, including Pd-mediated cross-couplings with aryl halides. By virtue of their favorable activities and exceptional selectivities, these Ir catalysts impart the synthetic versatility of arylboron reagents to C-H bonds in aromatic and heteroaromatic hydrocarbons.
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              Mild Iridium-Catalyzed Borylation of Arenes. High Turnover Numbers, Room Temperature Reactions, and Isolation of a Potential Intermediate

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                Author and article information

                Journal
                Bulletin of the Chemical Society of Japan
                BCSJ
                The Chemical Society of Japan
                0009-2673
                1348-0634
                December 15 2008
                December 15 2008
                : 81
                : 12
                : 1535-1553
                Article
                10.1246/bcsj.81.1535
                f3045ae2-8cca-41e7-b51d-a8559d7cde5a
                © 2008
                History

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