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Synthesis of the 1,5‐Benzothiazepane Scaffold – Established Methods and New Developments
The 1,5‐benzothiazepane structure is an important heterocyclic moiety present in a variety of commercial drugs and pharmaceuticals. This privileged scaffold exhibits a diversity of biological activities, including antimicrobial, antibacterial, anti‐epileptic, anti‐HIV, antidepressant, antithrombotic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9942483/ https://www.ncbi.nlm.nih.gov/pubmed/36807726 http://dx.doi.org/10.1002/open.202200262 |
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author | Ronse, Ulrike Magdalenić, Katarina Van Camp, John D'hooghe, Matthias |
author_facet | Ronse, Ulrike Magdalenić, Katarina Van Camp, John D'hooghe, Matthias |
author_sort | Ronse, Ulrike |
collection | PubMed |
description | The 1,5‐benzothiazepane structure is an important heterocyclic moiety present in a variety of commercial drugs and pharmaceuticals. This privileged scaffold exhibits a diversity of biological activities, including antimicrobial, antibacterial, anti‐epileptic, anti‐HIV, antidepressant, antithrombotic and anticancer properties. Its important pharmacological potential renders research into the development of new and efficient synthetic methods of high relevance. In the first part of this review, an overview of different synthetic approaches toward 1,5‐benzothiazepane and its derivatives is provided, ranging from established protocols to recent (enantioselective) methods that promote sustainability. In the second part, several structural characteristics influencing biological activity are briefly explored, providing a few insights into the structure‐activity relationships of these compounds. |
format | Online Article Text |
id | pubmed-9942483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99424832023-02-22 Synthesis of the 1,5‐Benzothiazepane Scaffold – Established Methods and New Developments Ronse, Ulrike Magdalenić, Katarina Van Camp, John D'hooghe, Matthias ChemistryOpen Reviews The 1,5‐benzothiazepane structure is an important heterocyclic moiety present in a variety of commercial drugs and pharmaceuticals. This privileged scaffold exhibits a diversity of biological activities, including antimicrobial, antibacterial, anti‐epileptic, anti‐HIV, antidepressant, antithrombotic and anticancer properties. Its important pharmacological potential renders research into the development of new and efficient synthetic methods of high relevance. In the first part of this review, an overview of different synthetic approaches toward 1,5‐benzothiazepane and its derivatives is provided, ranging from established protocols to recent (enantioselective) methods that promote sustainability. In the second part, several structural characteristics influencing biological activity are briefly explored, providing a few insights into the structure‐activity relationships of these compounds. John Wiley and Sons Inc. 2023-02-21 /pmc/articles/PMC9942483/ /pubmed/36807726 http://dx.doi.org/10.1002/open.202200262 Text en © 2023 The Authors. Published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Reviews Ronse, Ulrike Magdalenić, Katarina Van Camp, John D'hooghe, Matthias Synthesis of the 1,5‐Benzothiazepane Scaffold – Established Methods and New Developments |
title | Synthesis of the 1,5‐Benzothiazepane Scaffold – Established Methods and New Developments |
title_full | Synthesis of the 1,5‐Benzothiazepane Scaffold – Established Methods and New Developments |
title_fullStr | Synthesis of the 1,5‐Benzothiazepane Scaffold – Established Methods and New Developments |
title_full_unstemmed | Synthesis of the 1,5‐Benzothiazepane Scaffold – Established Methods and New Developments |
title_short | Synthesis of the 1,5‐Benzothiazepane Scaffold – Established Methods and New Developments |
title_sort | synthesis of the 1,5‐benzothiazepane scaffold – established methods and new developments |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9942483/ https://www.ncbi.nlm.nih.gov/pubmed/36807726 http://dx.doi.org/10.1002/open.202200262 |
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