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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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John Wiley and Sons Inc.
2017
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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. |
format | Online Article Text |
id | pubmed-5923600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT evansnicholash chiralcatenanesandrotaxanesfundamentalsandemergingapplications |