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Discovery of 5-(5,5-Dimethylbutenolide-3-ethylidene)-2-amino-imidazolinone Derivatives as Fungicidal Agents

The novel fungicidal agents 5-(5,5-dimethylbutenolide-3-ethylidene)-2-amino-imidazolinone derivatives, were designed and synthesized in moderate to excellent yields in four steps by α-hydroxyketone and diketene as raw materials and characterized by HR-ESI-MS and (1)H-NMR. The preliminary bioassay sh...

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Detalles Bibliográficos
Autores principales: Tang, Bo, Yang, Mingyan, Zhao, Yu, Kong, Lingqing, Wang, Weiwei, Wang, Mingan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332411/
https://www.ncbi.nlm.nih.gov/pubmed/26225953
http://dx.doi.org/10.3390/molecules200813740
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author Tang, Bo
Yang, Mingyan
Zhao, Yu
Kong, Lingqing
Wang, Weiwei
Wang, Mingan
author_facet Tang, Bo
Yang, Mingyan
Zhao, Yu
Kong, Lingqing
Wang, Weiwei
Wang, Mingan
author_sort Tang, Bo
collection PubMed
description The novel fungicidal agents 5-(5,5-dimethylbutenolide-3-ethylidene)-2-amino-imidazolinone derivatives, were designed and synthesized in moderate to excellent yields in four steps by α-hydroxyketone and diketene as raw materials and characterized by HR-ESI-MS and (1)H-NMR. The preliminary bioassay showed that some of these compounds, such as 4a, 4e and 5g exhibit 94.9%, 92.8% and 81.4% inhibition rates against Sclerotinia scleotiorum at the concentration of 50 µg/mL, respectively. The EC(50) values of compounds 4e and 4i were 4.14 and 3.27 µM against Alternaria Solani, and 5g had EC(50) value of 3.23 µM against S. scleotiorum. Compounds 4d and 4g displayed 98.0% and 97.8% control of spore germination against Botrytis cinerea at the concentration of 100 µg/mL, respectively.
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spelling pubmed-63324112019-01-24 Discovery of 5-(5,5-Dimethylbutenolide-3-ethylidene)-2-amino-imidazolinone Derivatives as Fungicidal Agents Tang, Bo Yang, Mingyan Zhao, Yu Kong, Lingqing Wang, Weiwei Wang, Mingan Molecules Article The novel fungicidal agents 5-(5,5-dimethylbutenolide-3-ethylidene)-2-amino-imidazolinone derivatives, were designed and synthesized in moderate to excellent yields in four steps by α-hydroxyketone and diketene as raw materials and characterized by HR-ESI-MS and (1)H-NMR. The preliminary bioassay showed that some of these compounds, such as 4a, 4e and 5g exhibit 94.9%, 92.8% and 81.4% inhibition rates against Sclerotinia scleotiorum at the concentration of 50 µg/mL, respectively. The EC(50) values of compounds 4e and 4i were 4.14 and 3.27 µM against Alternaria Solani, and 5g had EC(50) value of 3.23 µM against S. scleotiorum. Compounds 4d and 4g displayed 98.0% and 97.8% control of spore germination against Botrytis cinerea at the concentration of 100 µg/mL, respectively. MDPI 2015-07-28 /pmc/articles/PMC6332411/ /pubmed/26225953 http://dx.doi.org/10.3390/molecules200813740 Text en © 2015 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 license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tang, Bo
Yang, Mingyan
Zhao, Yu
Kong, Lingqing
Wang, Weiwei
Wang, Mingan
Discovery of 5-(5,5-Dimethylbutenolide-3-ethylidene)-2-amino-imidazolinone Derivatives as Fungicidal Agents
title Discovery of 5-(5,5-Dimethylbutenolide-3-ethylidene)-2-amino-imidazolinone Derivatives as Fungicidal Agents
title_full Discovery of 5-(5,5-Dimethylbutenolide-3-ethylidene)-2-amino-imidazolinone Derivatives as Fungicidal Agents
title_fullStr Discovery of 5-(5,5-Dimethylbutenolide-3-ethylidene)-2-amino-imidazolinone Derivatives as Fungicidal Agents
title_full_unstemmed Discovery of 5-(5,5-Dimethylbutenolide-3-ethylidene)-2-amino-imidazolinone Derivatives as Fungicidal Agents
title_short Discovery of 5-(5,5-Dimethylbutenolide-3-ethylidene)-2-amino-imidazolinone Derivatives as Fungicidal Agents
title_sort discovery of 5-(5,5-dimethylbutenolide-3-ethylidene)-2-amino-imidazolinone derivatives as fungicidal agents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332411/
https://www.ncbi.nlm.nih.gov/pubmed/26225953
http://dx.doi.org/10.3390/molecules200813740
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