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A happy medium: the synthesis of medicinally important medium-sized rings via ring expansion
Medium-sized rings have much promise in medicinal chemistry, but are difficult to make using direct cyclisation methods. In this minireview, we highlight the value of ring expansion strategies to address this long-standing synthetic challenge. We have drawn on recent progress (post 2013) to highligh...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152702/ https://www.ncbi.nlm.nih.gov/pubmed/34122787 http://dx.doi.org/10.1039/d0sc00568a |
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author | Clarke, Aimee K. Unsworth, William P. |
author_facet | Clarke, Aimee K. Unsworth, William P. |
author_sort | Clarke, Aimee K. |
collection | PubMed |
description | Medium-sized rings have much promise in medicinal chemistry, but are difficult to make using direct cyclisation methods. In this minireview, we highlight the value of ring expansion strategies to address this long-standing synthetic challenge. We have drawn on recent progress (post 2013) to highlight the key reaction design features that enable successful ‘normal-to-medium’ ring expansion for the synthesis of these medicinally important molecular frameworks, that are currently under-represented in compound screening collections and marketed drugs in view of their challenging syntheses. |
format | Online Article Text |
id | pubmed-8152702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-81527022021-06-11 A happy medium: the synthesis of medicinally important medium-sized rings via ring expansion Clarke, Aimee K. Unsworth, William P. Chem Sci Chemistry Medium-sized rings have much promise in medicinal chemistry, but are difficult to make using direct cyclisation methods. In this minireview, we highlight the value of ring expansion strategies to address this long-standing synthetic challenge. We have drawn on recent progress (post 2013) to highlight the key reaction design features that enable successful ‘normal-to-medium’ ring expansion for the synthesis of these medicinally important molecular frameworks, that are currently under-represented in compound screening collections and marketed drugs in view of their challenging syntheses. The Royal Society of Chemistry 2020-03-02 /pmc/articles/PMC8152702/ /pubmed/34122787 http://dx.doi.org/10.1039/d0sc00568a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Clarke, Aimee K. Unsworth, William P. A happy medium: the synthesis of medicinally important medium-sized rings via ring expansion |
title | A happy medium: the synthesis of medicinally important medium-sized rings via ring expansion |
title_full | A happy medium: the synthesis of medicinally important medium-sized rings via ring expansion |
title_fullStr | A happy medium: the synthesis of medicinally important medium-sized rings via ring expansion |
title_full_unstemmed | A happy medium: the synthesis of medicinally important medium-sized rings via ring expansion |
title_short | A happy medium: the synthesis of medicinally important medium-sized rings via ring expansion |
title_sort | happy medium: the synthesis of medicinally important medium-sized rings via ring expansion |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152702/ https://www.ncbi.nlm.nih.gov/pubmed/34122787 http://dx.doi.org/10.1039/d0sc00568a |
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