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      Reactions of Allenes with strong Borane‐Based Lewis Acids

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      European Journal of Organic Chemistry
      Wiley

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          Frustrated Lewis pair chemistry: development and perspectives.

          Frustrated Lewis pairs (FLPs) are combinations of Lewis acids and Lewis bases in solution that are deterred from strong adduct formation by steric and/or electronic factors. This opens pathways to novel cooperative reactions with added substrates. Small-molecule binding and activation by FLPs has led to the discovery of a variety of new reactions through unprecedented pathways. Hydrogen activation and subsequent manipulation in metal-free catalytic hydrogenations is a frequently observed feature of many FLPs. The current state of this young but rapidly expanding field is outlined in this Review and the future directions for its broadening sphere of impact are considered.
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            Frustrated Lewis Pairs.

            The articulation of the notion of "frustrated Lewis pairs" (FLPs), which emerged from the discovery that H2 can be reversibly activated by combinations of sterically encumbered Lewis acids and bases, has prompted a great deal of recent activity. Perhaps the most remarkable consequence has been the development of FLP catalysts for the hydrogenation of a range of organic substrates. In the past 9 years, the substrate scope has evolved from bulky polar species to include a wide range of unsaturated organic molecules. In addition, effective stereoselective metal-free hydrogenation catalysts have begun to emerge. The mechanism of this activation of H2 has been explored, and the nature and range of Lewis acid/base combinations capable of effecting such activation have also expanded to include a variety of non-metal species. The reactivity of FLPs with a variety of other small molecules, including olefins, alkynes, and a range of element oxides, has also been developed. Although much of this latter chemistry has uncovered unique stoichiometric transformations, metal-free catalytic hydroamination, CO2 reduction chemistry, and applications in polymerization have also been achieved. The concept is also beginning to find applications in bioinorganic and materials chemistry as well as heterogeneous catalysis. This Perspective highlights many of these developments and discusses the relationship between FLPs and established chemistry. Some of the directions and developments that are likely to emerge from FLP chemistry in the future are also presented.
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              Facile heterolytic cleavage of dihydrogen by phosphines and boranes.

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                Author and article information

                Journal
                European Journal of Organic Chemistry
                Eur. J. Org. Chem.
                Wiley
                1434-193X
                1099-0690
                September 07 2021
                September 2021
                September 07 2021
                : 2021
                : 33
                : 4707-4714
                Affiliations
                [1 ]Institut für Organische Chemie Justus-Liebig-Universität Gießen Heinrich-Buff-Ring-17 35392 Gießen Germany
                Article
                10.1002/ejoc.202100810
                174d6667-f7b2-4f92-b0ea-4a97235bf1f7
                © 2021

                http://creativecommons.org/licenses/by/4.0/

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

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