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Chiral Catenanes and Rotaxanes: Fundamentals and Emerging Applications

Molecular chirality provides a key challenge in host–guest recognition and other related chemical applications such as asymmetric catalysis. For a molecule to act as an efficient enantioselective receptor, it requires multi‐point interactions between host and chiral guest, which may be achieved by a...

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Autor principal: Evans, Nicholas H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923600/
https://www.ncbi.nlm.nih.gov/pubmed/29053181
http://dx.doi.org/10.1002/chem.201704149
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author Evans, Nicholas H.
author_facet Evans, Nicholas H.
author_sort Evans, Nicholas H.
collection PubMed
description Molecular chirality provides a key challenge in host–guest recognition and other related chemical applications such as asymmetric catalysis. For a molecule to act as an efficient enantioselective receptor, it requires multi‐point interactions between host and chiral guest, which may be achieved by an appropriate chiral 3D scaffold. As a consequence of their interlocked structure, catenanes and rotaxanes may present such a 3D scaffold, and can be chiral by inclusion of a classical chiral element and/or as a consequence of the mechanical bond. This Minireview presents illustrative examples of chiral [2]catenanes and [2]rotaxanes, and discusses where these molecules have been used in chemical applications such as chiral host–guest recognition and asymmetric catalysis.
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spelling pubmed-59236002018-05-07 Chiral Catenanes and Rotaxanes: Fundamentals and Emerging Applications Evans, Nicholas H. Chemistry Minireviews Molecular chirality provides a key challenge in host–guest recognition and other related chemical applications such as asymmetric catalysis. For a molecule to act as an efficient enantioselective receptor, it requires multi‐point interactions between host and chiral guest, which may be achieved by an appropriate chiral 3D scaffold. As a consequence of their interlocked structure, catenanes and rotaxanes may present such a 3D scaffold, and can be chiral by inclusion of a classical chiral element and/or as a consequence of the mechanical bond. This Minireview presents illustrative examples of chiral [2]catenanes and [2]rotaxanes, and discusses where these molecules have been used in chemical applications such as chiral host–guest recognition and asymmetric catalysis. John Wiley and Sons Inc. 2017-11-30 2018-03-02 /pmc/articles/PMC5923600/ /pubmed/29053181 http://dx.doi.org/10.1002/chem.201704149 Text en © 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Minireviews
Evans, Nicholas H.
Chiral Catenanes and Rotaxanes: Fundamentals and Emerging Applications
title Chiral Catenanes and Rotaxanes: Fundamentals and Emerging Applications
title_full Chiral Catenanes and Rotaxanes: Fundamentals and Emerging Applications
title_fullStr Chiral Catenanes and Rotaxanes: Fundamentals and Emerging Applications
title_full_unstemmed Chiral Catenanes and Rotaxanes: Fundamentals and Emerging Applications
title_short Chiral Catenanes and Rotaxanes: Fundamentals and Emerging Applications
title_sort chiral catenanes and rotaxanes: fundamentals and emerging applications
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923600/
https://www.ncbi.nlm.nih.gov/pubmed/29053181
http://dx.doi.org/10.1002/chem.201704149
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