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Synthetic Approaches to Biologically Active C-2-Substituted Benzothiazoles
Numerous benzothiazole derivatives are used in organic synthesis, in various industrial and consumer products, and in drugs, with a wide spectrum of biological activity. As the properties of the benzothiazole moiety are strongly affected by the nature and position of substitutions, in this review, c...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9027766/ https://www.ncbi.nlm.nih.gov/pubmed/35458794 http://dx.doi.org/10.3390/molecules27082598 |
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author | Shainyan, Bagrat A. Zhilitskaya, Larisa V. Yarosh, Nina O. |
author_facet | Shainyan, Bagrat A. Zhilitskaya, Larisa V. Yarosh, Nina O. |
author_sort | Shainyan, Bagrat A. |
collection | PubMed |
description | Numerous benzothiazole derivatives are used in organic synthesis, in various industrial and consumer products, and in drugs, with a wide spectrum of biological activity. As the properties of the benzothiazole moiety are strongly affected by the nature and position of substitutions, in this review, covering the literature from 2016, we focus on C-2-substituted benzothiazoles, including the methods of their synthesis, structural modification, reaction mechanisms, and possible pharmacological activity. The synthetic approaches to these heterocycles include both traditional multistep reactions and one-pot atom economy processes using green chemistry principles and easily available reagents. Special attention is paid to the methods of the thiazole ring closure and chemical modification by the introduction of pharmacophore groups. |
format | Online Article Text |
id | pubmed-9027766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90277662022-04-23 Synthetic Approaches to Biologically Active C-2-Substituted Benzothiazoles Shainyan, Bagrat A. Zhilitskaya, Larisa V. Yarosh, Nina O. Molecules Review Numerous benzothiazole derivatives are used in organic synthesis, in various industrial and consumer products, and in drugs, with a wide spectrum of biological activity. As the properties of the benzothiazole moiety are strongly affected by the nature and position of substitutions, in this review, covering the literature from 2016, we focus on C-2-substituted benzothiazoles, including the methods of their synthesis, structural modification, reaction mechanisms, and possible pharmacological activity. The synthetic approaches to these heterocycles include both traditional multistep reactions and one-pot atom economy processes using green chemistry principles and easily available reagents. Special attention is paid to the methods of the thiazole ring closure and chemical modification by the introduction of pharmacophore groups. MDPI 2022-04-18 /pmc/articles/PMC9027766/ /pubmed/35458794 http://dx.doi.org/10.3390/molecules27082598 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Shainyan, Bagrat A. Zhilitskaya, Larisa V. Yarosh, Nina O. Synthetic Approaches to Biologically Active C-2-Substituted Benzothiazoles |
title | Synthetic Approaches to Biologically Active C-2-Substituted Benzothiazoles |
title_full | Synthetic Approaches to Biologically Active C-2-Substituted Benzothiazoles |
title_fullStr | Synthetic Approaches to Biologically Active C-2-Substituted Benzothiazoles |
title_full_unstemmed | Synthetic Approaches to Biologically Active C-2-Substituted Benzothiazoles |
title_short | Synthetic Approaches to Biologically Active C-2-Substituted Benzothiazoles |
title_sort | synthetic approaches to biologically active c-2-substituted benzothiazoles |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9027766/ https://www.ncbi.nlm.nih.gov/pubmed/35458794 http://dx.doi.org/10.3390/molecules27082598 |
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