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      Strain release – an old tool for new transformations

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          Abstract

          This Feature Article provides an overview of research advances in the chemistry of spring-loaded molecules, focusing mainly on strain-release transformations.

          Abstract

          Strain-release driven transformations give access to attractive bioisosteric motifs highly prized by medicinal chemists and they are characteristic of molecules possessing distorted bond lengths and angles. By broadening the chemical space in drug discovery, recently, these compounds have attracted a lot of interest. Their reactivity stems mainly from an increased energy and destabilization. As a result, the opening of the bridging bond occurs under the action of both nucleophiles and electrophiles as well as radical species and transition metals. Though the bridge bond dominates their reactivity, it is also influenced by the substitution pattern. This feature article focuses on strain-release driven strategies paying particular attention to the most recent (year > 2010) advances.

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          The Chemistry of the Cyclopropyl Group

          S Hoz, Hoz (1987)
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            Author and article information

            Contributors
            (View ORCID Profile)
            (View ORCID Profile)
            Journal
            CHCOFS
            Chemical Communications
            Chem. Commun.
            Royal Society of Chemistry (RSC)
            1359-7345
            1364-548X
            May 28 2020
            2020
            : 56
            : 43
            : 5718-5734
            Affiliations
            [1 ]Institute of Organic Chemistry Polish Academy of Sciences
            [2 ]Warsaw 01-224
            [3 ]Poland
            [4 ]Department of Chemistry
            [5 ]Warsaw University of Technology
            Article
            10.1039/D0CC01771J
            32391543
            287f2b81-5cb7-42a1-a014-f4f6825af4ce
            © 2020

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

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