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      Stapled Peptides by Late-Stage C(sp3)−H Activation

      , , ,
      Angewandte Chemie International Edition
      Wiley-Blackwell

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          Aryl-aryl bond formation by transition-metal-catalyzed direct arylation.

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            C-H bond functionalization: emerging synthetic tools for natural products and pharmaceuticals.

            The direct functionalization of C-H bonds in organic compounds has recently emerged as a powerful and ideal method for the formation of carbon-carbon and carbon-heteroatom bonds. This Review provides an overview of C-H bond functionalization strategies for the rapid synthesis of biologically active compounds such as natural products and pharmaceutical targets. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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              Catalytic Functionalization of C(sp2)H and C(sp3)H Bonds by Using Bidentate Directing Groups

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                Author and article information

                Journal
                Angewandte Chemie International Edition
                Angew. Chem. Int. Ed.
                Wiley-Blackwell
                14337851
                January 02 2017
                January 02 2017
                : 56
                : 1
                : 314-318
                Article
                10.1002/anie.201608648
                12080b49-dd76-4a55-8aae-e68f339c5aa4
                © 2017

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

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