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      Convenient and Mild Epoxidation of Alkenes Using Heterogeneous Cobalt Oxide Catalysts

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          Heterogenized cobalt oxide catalysts for nitroarene reduction by pyrolysis of molecularly defined complexes.

          Molecularly well-defined homogeneous catalysts are known for a wide variety of chemical transformations. The effect of small changes in molecular structure can be studied in detail and used to optimize many processes. However, many industrial processes require heterogeneous catalysts because of their stability, ease of separation and recyclability, but these are more difficult to control on a molecular level. Here, we describe the conversion of homogeneous cobalt complexes into heterogeneous cobalt oxide catalysts via immobilization and pyrolysis on activated carbon. The catalysts thus produced are useful for the industrially important reduction of nitroarenes to anilines. The ligand indirectly controls the selectivity and activity of the recyclable catalyst and catalyst optimization can be performed at the level of the solution-phase precursor before conversion into the active heterogeneous catalyst.
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            CuBr-catalyzed efficient alkynylation of sp3 C-H bonds adjacent to a nitrogen atom.

            A simple and effective catalytic method to construct propargylamine was developed by using copper bromide and tert-BuOOH via a combination of sp3 C-H bond and sp C-H bond activations followed by C-C bond formation.
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              Highly efficient oxidative amidation of aldehydes with amine hydrochloride salts.

              A mild and efficient copper-catalyzed oxidative amidation of aldehydes was developed using amine HCl salts and tert-butyl hydroperoxide as an oxidant.
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                Author and article information

                Journal
                Angewandte Chemie International Edition
                Angew. Chem. Int. Ed.
                Wiley-Blackwell
                14337851
                April 22 2014
                April 22 2014
                : 53
                : 17
                : 4359-4363
                Article
                10.1002/anie.201310420
                b4b7bdad-40f1-473a-b41c-84367aafddef
                © 2014

                http://doi.wiley.com/10.1002/tdm_license_1.1

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