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      Looking deep into C–H functionalization: the synthesis and application of cyclopentadienyl and related metal catalysts

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          Abstract

          This feature review is focused on recent key applications of commonly used transition-metal Cp-type catalysts for C–H bond functionalizations.

          Abstract

          Metal catalyzed C–H functionalization offers a versatile platform for methodology development and a wide variety of reactions now exist for the chemo- and site-selective functionalization of organic molecules. Cyclopentadienyl-metal (CpM) complexes of transition metals and their correlative analogues have found widespread application in this area, and herein we highlight several key applications of commonly used transition-metal Cp-type catalysts. In addition, an understanding of transition metal Cp-type catalyst synthesis is important, particularly where modifications to the catalyst structure are required for different applications, and a summary of this aspect is given.

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          Rhodium-catalyzed C-C bond formation via heteroatom-directed C-H bond activation.

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            Towards mild metal-catalyzed C-H bond activation.

            Functionalizing traditionally inert carbon-hydrogen bonds represents a powerful transformation in organic synthesis, providing new entries to valuable structural motifs and improving the overall synthetic efficiency. C-H bond activation, however, often necessitates harsh reaction conditions that result in functional group incompatibilities and limited substrate scope. An understanding of the reaction mechanism and rational design of experimental conditions have led to significant improvement in both selectivity and applicability. This critical review summarizes and discusses endeavours towards the development of mild C-H activation methods and wishes to trigger more research towards this goal. In addition, we examine select examples in complex natural product synthesis to demonstrate the synthetic utility of mild C-H functionalization (84 references). This journal is © The Royal Society of Chemistry 2011
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              Recent advances in homogeneous nickel catalysis.

              Tremendous advances have been made in nickel catalysis over the past decade. Several key properties of nickel, such as facile oxidative addition and ready access to multiple oxidation states, have allowed the development of a broad range of innovative reactions. In recent years, these properties have been increasingly understood and used to perform transformations long considered exceptionally challenging. Here we discuss some of the most recent and significant developments in homogeneous nickel catalysis, with an emphasis on both synthetic outcome and mechanism.
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                Author and article information

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                Journal
                CHCOFS
                Chemical Communications
                Chem. Commun.
                Royal Society of Chemistry (RSC)
                1359-7345
                1364-548X
                March 03 2022
                2022
                : 58
                : 19
                : 3101-3121
                Affiliations
                [1 ]Institute of Exact Sciences, Department of Chemistry, Federal University of Minas Gerais - UFMG, Belo Horizonte, 31270-901, MG, Brazil
                [2 ]Centre for Excellence for Research in Sustainable Chemistry (CERSusChem), Department of Chemistry, Federal University of São Carlos, UFSCar, 13565-905, Brazil
                [3 ]Department of Chemistry, Fluminense Federal University, Niteroi, 24020-141, RJ, Brazil
                [4 ]Department of Chemistry, University of Liverpool, Crown Street, Liverpool, L69 7ZD, UK
                Article
                10.1039/D1CC07040A
                2fdfa71e-a7c8-4395-993b-7dff53dc6ce2
                © 2022

                http://rsc.li/journals-terms-of-use

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