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      Alkene versus Aryl Chlorination in Asymmetric Hypervalent Iodine Catalysis: A Case Study

      , , ,
      Synlett
      Georg Thieme Verlag KG

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          Abstract

          Hypervalent λ3-iodanes have become a prominent tool for halofunctionalizations of alkenes. Despite many examples of asymmetric fluorinations reported lately, the corresponding enantioselective chlorination reactions using iodoresorcinol-based catalysts are significantly less developed, with only one example known to date. Here, we show how competing aromatic chlorination of the iodoarene catalyst is a significant obstacle in these transformations, hinting towards a conceptual issue with this well-established catalyst class for enantioselective chlorinations. Consequently, the reaction conditions and the catalyst design must be adapted to facilitate an effective chirality transfer. Hence, attention should be paid when selecting the oxidizing agent, the stoichiometry, and careful reaction analysis must be conducted to identify the factual catalytically active species.

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          Most cited references81

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          Advances in Synthetic Applications of Hypervalent Iodine Compounds.

          The preparation, structure, and chemistry of hypervalent iodine compounds are reviewed with emphasis on their synthetic application. Compounds of iodine possess reactivity similar to that of transition metals, but have the advantage of environmental sustainability and efficient utilization of natural resources. These compounds are widely used in organic synthesis as selective oxidants and environmentally friendly reagents. Synthetic uses of hypervalent iodine reagents in halogenation reactions, various oxidations, rearrangements, aminations, C-C bond-forming reactions, and transition metal-catalyzed reactions are summarized and discussed. Recent discovery of hypervalent catalytic systems and recyclable reagents, and the development of new enantioselective reactions using chiral hypervalent iodine compounds represent a particularly important achievement in the field of hypervalent iodine chemistry. One of the goals of this Review is to attract the attention of the scientific community as to the benefits of using hypervalent iodine compounds as an environmentally sustainable alternative to heavy metals.
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            Hypervalent iodine reagents as a new entrance to organocatalysts

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              Novel 10-I-3 hypervalent iodine-based compounds for electrophilic trifluoromethylation.

              The synthesis of a new family of 10-I-3 hypervalent iodine compounds is described in which the CF3 functionality participates directly in the hypervalent bond. These materials are accessible by nucleophilic ligand substitution at iodine using Me3SiCF3 in the presence of a substoichiometric amount of fluoride. The expected T-shaped geometry at iodine was verified by X-ray crystallographic analyses of three of the products (1-trifluoromethyl-1,2-benziodoxol-3-(1 H)-one and two substituted 1-trifluoromethyl-1,3-dihydro-1,2-benziodoxoles). Preliminary results for the direct electrophilic transfer of the trifluoromethyl moiety onto organic nucleophiles show modest reactivity in polar aprotic solvents under relatively mild conditions. The overall process can be understood as a formal umpolung of the CF3 group.

                Author and article information

                Contributors
                Journal
                Synlett
                Synlett
                Georg Thieme Verlag KG
                0936-5214
                1437-2096
                May 13 2024
                June 2024
                October 30 2023
                December 06 2023
                June 2024
                : 35
                : 09
                : 1001-1006
                Article
                10.1055/a-2201-7326
                966abc06-0ca0-4a44-9171-352062a9822d
                © 2024
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