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Synthesis and Herbicidal Activity of Substituted Pyrazole Isothiocyanates
Isothiocyanates and substituted pyrazoles were combined to form a series of novel isothiocyanates with highly effective herbicidal activity. The target compounds were analyzed by elemental analysis, (1)H-NMR, EI-MS and IR spectroscopy. The synthesized compounds, particularly compounds 3-1 and 3-7, e...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268192/ https://www.ncbi.nlm.nih.gov/pubmed/23075815 http://dx.doi.org/10.3390/molecules171012187 |
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author | Wu, Hua Feng, Jun-Tao Lin, Kai-Chun Zhang, Xing |
author_facet | Wu, Hua Feng, Jun-Tao Lin, Kai-Chun Zhang, Xing |
author_sort | Wu, Hua |
collection | PubMed |
description | Isothiocyanates and substituted pyrazoles were combined to form a series of novel isothiocyanates with highly effective herbicidal activity. The target compounds were analyzed by elemental analysis, (1)H-NMR, EI-MS and IR spectroscopy. The synthesized compounds, particularly compounds 3-1 and 3-7, exhibited good herbicidal activities against four weeds. The EC(50) values of compound 3-1 against Echinochloa crusgalli L., Cyperus iria L., Dactylis glomerata L., and Trifolium repens L. were 64.32, 65.83, 62.42, and 67.72 µg/mL, respectively. The EC(50) values of compound 3-7 against E. crusgalli L., C. iria L., D. glomerata L., T. repens L. were 65.33, 64.90, 59.41 and 67.41 µg/mL, respectively. Compounds 3-1 and 3-7 may be further optimized as lead compounds for new herbicides. |
format | Online Article Text |
id | pubmed-6268192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62681922018-12-12 Synthesis and Herbicidal Activity of Substituted Pyrazole Isothiocyanates Wu, Hua Feng, Jun-Tao Lin, Kai-Chun Zhang, Xing Molecules Article Isothiocyanates and substituted pyrazoles were combined to form a series of novel isothiocyanates with highly effective herbicidal activity. The target compounds were analyzed by elemental analysis, (1)H-NMR, EI-MS and IR spectroscopy. The synthesized compounds, particularly compounds 3-1 and 3-7, exhibited good herbicidal activities against four weeds. The EC(50) values of compound 3-1 against Echinochloa crusgalli L., Cyperus iria L., Dactylis glomerata L., and Trifolium repens L. were 64.32, 65.83, 62.42, and 67.72 µg/mL, respectively. The EC(50) values of compound 3-7 against E. crusgalli L., C. iria L., D. glomerata L., T. repens L. were 65.33, 64.90, 59.41 and 67.41 µg/mL, respectively. Compounds 3-1 and 3-7 may be further optimized as lead compounds for new herbicides. MDPI 2012-10-17 /pmc/articles/PMC6268192/ /pubmed/23075815 http://dx.doi.org/10.3390/molecules171012187 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Wu, Hua Feng, Jun-Tao Lin, Kai-Chun Zhang, Xing Synthesis and Herbicidal Activity of Substituted Pyrazole Isothiocyanates |
title | Synthesis and Herbicidal Activity of Substituted Pyrazole Isothiocyanates |
title_full | Synthesis and Herbicidal Activity of Substituted Pyrazole Isothiocyanates |
title_fullStr | Synthesis and Herbicidal Activity of Substituted Pyrazole Isothiocyanates |
title_full_unstemmed | Synthesis and Herbicidal Activity of Substituted Pyrazole Isothiocyanates |
title_short | Synthesis and Herbicidal Activity of Substituted Pyrazole Isothiocyanates |
title_sort | synthesis and herbicidal activity of substituted pyrazole isothiocyanates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268192/ https://www.ncbi.nlm.nih.gov/pubmed/23075815 http://dx.doi.org/10.3390/molecules171012187 |
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