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Concise Total Synthesis and Antifungal Activities of Fusaric Acid, a Natural Product
The total synthesis of a natural product alkaloid fusaric acid (FA), which exhibits herbicide, fungicide, insecticide and even diverse notable pharmacological activities, was accomplished in four steps using commercially available materials. The synthesis, based on a unified and flexible strategy us...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503603/ https://www.ncbi.nlm.nih.gov/pubmed/32854261 http://dx.doi.org/10.3390/molecules25173859 |
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author | Huang, Bin Bin Liu, Ya Yi Zhu, Peng Fei Jiang, Yi Cheng Ouyang, Ming-An |
author_facet | Huang, Bin Bin Liu, Ya Yi Zhu, Peng Fei Jiang, Yi Cheng Ouyang, Ming-An |
author_sort | Huang, Bin Bin |
collection | PubMed |
description | The total synthesis of a natural product alkaloid fusaric acid (FA), which exhibits herbicide, fungicide, insecticide and even diverse notable pharmacological activities, was accomplished in four steps using commercially available materials. The synthesis, based on a unified and flexible strategy using 6-bromonicotinaldehyde as a common intermediate, is concise, convergent, practical and can be carried out on a two-gram scale. This approach could be readily applicable to the synthesis of its analogues. In addition, FA had a wide range of inhibitory activities against 14 plant pathogenic fungi in this study, which demonstrated that as a leading compound, and it has great potential to be further developed as an agricultural fungicide. |
format | Online Article Text |
id | pubmed-7503603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75036032020-09-27 Concise Total Synthesis and Antifungal Activities of Fusaric Acid, a Natural Product Huang, Bin Bin Liu, Ya Yi Zhu, Peng Fei Jiang, Yi Cheng Ouyang, Ming-An Molecules Communication The total synthesis of a natural product alkaloid fusaric acid (FA), which exhibits herbicide, fungicide, insecticide and even diverse notable pharmacological activities, was accomplished in four steps using commercially available materials. The synthesis, based on a unified and flexible strategy using 6-bromonicotinaldehyde as a common intermediate, is concise, convergent, practical and can be carried out on a two-gram scale. This approach could be readily applicable to the synthesis of its analogues. In addition, FA had a wide range of inhibitory activities against 14 plant pathogenic fungi in this study, which demonstrated that as a leading compound, and it has great potential to be further developed as an agricultural fungicide. MDPI 2020-08-25 /pmc/articles/PMC7503603/ /pubmed/32854261 http://dx.doi.org/10.3390/molecules25173859 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Huang, Bin Bin Liu, Ya Yi Zhu, Peng Fei Jiang, Yi Cheng Ouyang, Ming-An Concise Total Synthesis and Antifungal Activities of Fusaric Acid, a Natural Product |
title | Concise Total Synthesis and Antifungal Activities of Fusaric Acid, a Natural Product |
title_full | Concise Total Synthesis and Antifungal Activities of Fusaric Acid, a Natural Product |
title_fullStr | Concise Total Synthesis and Antifungal Activities of Fusaric Acid, a Natural Product |
title_full_unstemmed | Concise Total Synthesis and Antifungal Activities of Fusaric Acid, a Natural Product |
title_short | Concise Total Synthesis and Antifungal Activities of Fusaric Acid, a Natural Product |
title_sort | concise total synthesis and antifungal activities of fusaric acid, a natural product |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503603/ https://www.ncbi.nlm.nih.gov/pubmed/32854261 http://dx.doi.org/10.3390/molecules25173859 |
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