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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...

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Autores principales: Wu, Hua, Feng, Jun-Tao, Lin, Kai-Chun, Zhang, Xing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
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.
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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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