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An Overview on the Synthesis of Fused Pyridocoumarins with Biological Interest
Pyridocoumarins are a class of synthetic and naturally occurring organic compounds with interesting biological activities. This review focuses on the synthetic strategies for the synthesis of pyridocoumarins and presents the biological properties of those compounds. The synthesis involves the format...
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/PMC9658346/ https://www.ncbi.nlm.nih.gov/pubmed/36364083 http://dx.doi.org/10.3390/molecules27217256 |
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author | Douka, Matina D. Litinas, Konstantinos E. |
author_facet | Douka, Matina D. Litinas, Konstantinos E. |
author_sort | Douka, Matina D. |
collection | PubMed |
description | Pyridocoumarins are a class of synthetic and naturally occurring organic compounds with interesting biological activities. This review focuses on the synthetic strategies for the synthesis of pyridocoumarins and presents the biological properties of those compounds. The synthesis involves the formation of the pyridine ring, at first, from a coumarin derivative, such as aminocoumarins, hydroxycoumarins, or other coumarins. The formation of a pyranone moiety follows from an existing pyridine or piperidine or phenol derivative. For the above syntheses, [4 + 2] cycloaddition reactions, multi-component reactions (MCR), as well as metal-catalyzed reactions, are useful. Pyridocoumarins present anti-cancer, anti-HIV, antimalarial, analgesic, antidiabetic, antibacterial, antifungal, anti-inflammatory, and antioxidant activities. |
format | Online Article Text |
id | pubmed-9658346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96583462022-11-15 An Overview on the Synthesis of Fused Pyridocoumarins with Biological Interest Douka, Matina D. Litinas, Konstantinos E. Molecules Review Pyridocoumarins are a class of synthetic and naturally occurring organic compounds with interesting biological activities. This review focuses on the synthetic strategies for the synthesis of pyridocoumarins and presents the biological properties of those compounds. The synthesis involves the formation of the pyridine ring, at first, from a coumarin derivative, such as aminocoumarins, hydroxycoumarins, or other coumarins. The formation of a pyranone moiety follows from an existing pyridine or piperidine or phenol derivative. For the above syntheses, [4 + 2] cycloaddition reactions, multi-component reactions (MCR), as well as metal-catalyzed reactions, are useful. Pyridocoumarins present anti-cancer, anti-HIV, antimalarial, analgesic, antidiabetic, antibacterial, antifungal, anti-inflammatory, and antioxidant activities. MDPI 2022-10-26 /pmc/articles/PMC9658346/ /pubmed/36364083 http://dx.doi.org/10.3390/molecules27217256 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 Douka, Matina D. Litinas, Konstantinos E. An Overview on the Synthesis of Fused Pyridocoumarins with Biological Interest |
title | An Overview on the Synthesis of Fused Pyridocoumarins with Biological Interest |
title_full | An Overview on the Synthesis of Fused Pyridocoumarins with Biological Interest |
title_fullStr | An Overview on the Synthesis of Fused Pyridocoumarins with Biological Interest |
title_full_unstemmed | An Overview on the Synthesis of Fused Pyridocoumarins with Biological Interest |
title_short | An Overview on the Synthesis of Fused Pyridocoumarins with Biological Interest |
title_sort | overview on the synthesis of fused pyridocoumarins with biological interest |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9658346/ https://www.ncbi.nlm.nih.gov/pubmed/36364083 http://dx.doi.org/10.3390/molecules27217256 |
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