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Covalently Templated Syntheses of Mechanically Interlocked Molecules

Title: Covalently Templated Syntheses of Mechanically Interlocked Molecules
Authors: van Maarseveen, Jan H.; Cornelissen, Milo D.; Pilon, Simone
Contributors: Nederlandse Organisatie voor Wetenschappelijk Onderzoek
Source: Synthesis ; volume 53, issue 24, page 4527-4548 ; ISSN 0039-7881 1437-210X
Publisher Information: Georg Thieme Verlag KG
Publication Year: 2021
Description: Mechanically interlocked molecules (MiMs), such as catenanes and rotaxanes, exhibit unique properties due to the mechanical bond which unites their components. The translational and rotational freedom present in these compounds may be harnessed to create stimuli-responsive MiMs, which find potential application as artificial molecular machines. Mechanically interlocked structures such as lasso peptides have also been found in nature, making MiMs promising albeit elusive targets for drug discovery. Although the first syntheses of MiMs were based on covalent strategies, approaches based on non-covalent interactions rose to prominence thereafter and have remained dominant. Non-covalent strategies are generally short and efficient, but do require particular structural motifs which are difficult to alter. In a covalent approach, MiMs can be more easily modified while the components may have increased rotational and translational freedom. Both approaches have complementary merits and combining the unmatched efficiency of non-covalent approaches with the scope of covalent syntheses may open up vast opportunities. In this review, recent covalently templated syntheses of MiMs are discussed to show their complementarity and anticipate future developments in this field. 1 Introduction 2 Tetrahedral Templates 2.1 A Carbonate Template for Non-Rusty Catenanes 2.2 All-Benzene Catenanes on a Silicon Template 2.3 Backfolding from Quaternary Carbon 3 Planar Templates 3.1 Rotaxanes Constructed in a Ring 3.2 Hydrindacene as a Dynamic Covalent Template 3.3 Templating on Tri- and Tetrasubstituted Benzenes 4 Conclusion
Document Type: article in journal/newspaper
Language: English
DOI: 10.1055/a-1665-4650
DOI: 10.1055/a-1665-4650.pdf
Availability: https://doi.org/10.1055/a-1665-4650; http://www.thieme-connect.de/products/ejournals/pdf/10.1055/a-1665-4650.pdf
Rights: https://creativecommons.org/licenses/by-nc-nd/4.0/
Accession Number: edsbas.52817FB2
Database: BASE