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      Walking Metals for Remote Functionalization

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          Abstract

          The distant and selective activation of unreactive C–H and C–C bonds remains one of the biggest challenges in organic chemistry. In recent years, the development of remote functionalization has received growing interest as it allows for the activation of rather challenging C–H and C–C bonds distant from the initiation point by means of a “metal-walk”. A “metal-walk” or “chain-walk” is defined by an iterative series of consecutive 1,2- or 1,3-hydride shifts of a metal complex along a single hydrocarbon chain. With this approach, simple building blocks or mixtures thereof can be transformed into complex scaffolds in a convergent and unified strategy. A variety of catalytic systems have been developed and refined over the past decade ranging from late-transition-metal complexes to more sustainable iron- and cobalt-based systems. As the possibilities of this field are slowly unfolding, this area of research will contribute considerably to provide solutions to yet unmet synthetic challenges.

          Abstract

          The transition-metal-catalyzed remote functionalization of olefins is highlighted with a special emphasis on the most recent developments of this emerging area of research.

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          Organometallic chemistry: C-H activation.

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            Mild metal-catalyzed C-H activation: examples and concepts.

            Organic reactions that involve the direct functionalization of non-activated C-H bonds represent an attractive class of transformations which maximize atom- and step-economy, and simplify chemical synthesis. Due to the high stability of C-H bonds, these processes, however, have most often required harsh reaction conditions, which has drastically limited their use as tools for the synthesis of complex organic molecules. Following the increased understanding of mechanistic aspects of C-H activation gained over recent years, great strides have been taken to design and develop new protocols that proceed efficiently under mild conditions and duly benefit from improved functional group tolerance and selectivity. In this review, we present the current state of the art in this field and detail C-H activation transformations reported since 2011 that proceed either at or below ambient temperature, in the absence of strongly acidic or basic additives or without strong oxidants. Furthermore, by identifying and discussing the major strategies that have led to these improvements, we hope that this review will serve as a useful conceptual overview and inspire the next generation of mild C-H transformations.
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              New Pd(II)- and Ni(II)-Based Catalysts for Polymerization of Ethylene and .alpha.-Olefins

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                Author and article information

                Journal
                ACS Cent Sci
                ACS Cent Sci
                oc
                acscii
                ACS Central Science
                American Chemical Society
                2374-7943
                2374-7951
                08 February 2018
                28 February 2018
                : 4
                : 2
                : 153-165
                Affiliations
                [§ ]Institute of Chemical Research of Catalonia (ICIQ), The Barcelona Institute of Science and Technology , Avinguda dels Països Catalans, 16, 43007 Tarragona, Spain
                []ICREA , Passeig Lluïs Companys, 23, 08010 Barcelona, Spain
                []Schulich Faculty of Chemistry, Technion—Israel Institute of Technology , 32000 Haifa, Israel
                Author notes
                Article
                10.1021/acscentsci.8b00005
                5833012
                29532015
                234e7999-ee5f-4e6b-9a39-65a20fa83342
                Copyright © 2018 American Chemical Society

                This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.

                History
                : 03 January 2018
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                Custom metadata
                oc8b00005
                oc-2018-00005r

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