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      Selective and synergistic cobalt(III)-catalyzed three-component C–H bond addition to dienes and aldehydes

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          Abstract

          Two-component C–H bond additions to a large variety of coupling partners have been developed with applications towards materials, natural product and drug synthesis. Sequential three-component C–H bond addition across two different coupling partners potentially enables the convergent synthesis of complex molecular scaffolds from simple precursors. Here, we report three-component Co(III)-catalyzed C–H bond additions to dienes and aldehydes that proceeds with high regio- and stereoselectivity resulting in two new carbon-carbon σ-bonds and from four to six new stereocenters. The reaction relies on the synergistic reactivity of the diene and aldehyde with neither undergoing C–H bond addition alone. A detailed mechanism is supported by X-ray structural characterization of a Co(III)-allyl intermediate, observed transfer of stereochemical information, and kinetic isotope studies. The applicability of the method to biologically relevant molecules is exemplified by the rapid synthesis of the western fragment of the complex ionophore antibiotic lasalocid A.

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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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            C-H bond activation enables the rapid construction and late-stage diversification of functional molecules.

            The beginning of the twenty-first century has witnessed significant advances in the field of C-H bond activation, and this transformation is now an established piece in the synthetic chemists' toolbox. This methodology has the potential to be used in many different areas of chemistry, for example it provides a perfect opportunity for the late-stage diversification of various kinds of organic scaffolds, ranging from relatively small molecules like drug candidates, to complex polydisperse organic compounds such as polymers. In this way, C-H activation approaches enable relatively straightforward access to a plethora of analogues or can help to streamline the lead-optimization phase. Furthermore, synthetic pathways for the construction of complex organic materials can now be designed that are more atom- and step-economical than previous methods and, in some cases, can be based on synthetic disconnections that are just not possible without C-H activation. This Perspective highlights the potential of metal-catalysed C-H bond activation reactions, which now extend beyond the field of traditional synthetic organic chemistry.
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              On the Interpretation of Deuterium Kinetic Isotope Effects in CH Bond Functionalizations by Transition-Metal Complexes

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                Author and article information

                Journal
                101714581
                46967
                Nat Catal
                Nat Catal
                Nature catalysis
                2520-1158
                6 July 2018
                2018
                13 September 2018
                : 1
                : 673-679
                Affiliations
                Department of Chemistry, Yale University, 225 Prospect St., New Haven, CT 06520 (USA)
                Author notes

                Author Contributions

                J.A.B. co-conceived the concept and developed the reaction conditions. J.A.B. completed the scope with respect to C–H bond substrates, including the lasalocid A derivative, conducted the mechanistic experiments, and co-prepared the manuscript. S.M. helped with the development of the reaction conditions, and completed the scope with respect to both aldehyde and diene coupling partners. S.M. also helped with the preparation of the manuscript. S.K.W. helped with the completion of the scope with respect to C–H bond substrates. B.Q.M. solved the X-ray crystal structures of compounds 4b, 4ar’, and 8a. J.A.E. co-conceived the concept and co-prepared the manuscript with feedback from J.A.B. and S.M.</author_notes>

                Corresponding author: Correspondence to Jonathan A. Ellman ( jonathan.ellman@ 123456yale.edu ).
                Article
                NIHMS979943
                10.1038/s41929-018-0123-4
                6136669
                875f9a2b-59f8-46d5-88c4-6a7aae0778ac

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