Synthesis and Fungicidal Activity of Pyrazolecarboxamide Containing α-Aminoacetanilide Moiety
A series of pyrazolecarboxamides containing α-aminoacetanilide moiety (4) were synthesized. These compounds were characterized by IR, MS and 1H NMR. Their fugicidal activities against Rhizoctonia solani, Sclerotinia sclerotiorum, Monilinia fructicola and Alternaria brassicae were evaluated. The resu...
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| Format: | Article |
| Language: | English |
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Wiley
2012-01-01
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| Series: | E-Journal of Chemistry |
| Online Access: | http://dx.doi.org/10.1155/2012/863135 |
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| _version_ | 1832556566317891584 |
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| author | Zhi-Yong Fang Hong Jiang Xiao-Dong Ye |
| author_facet | Zhi-Yong Fang Hong Jiang Xiao-Dong Ye |
| author_sort | Zhi-Yong Fang |
| collection | DOAJ |
| description | A series of pyrazolecarboxamides containing α-aminoacetanilide moiety (4) were synthesized. These compounds were characterized by IR, MS and 1H NMR. Their fugicidal activities against Rhizoctonia solani, Sclerotinia sclerotiorum, Monilinia fructicola and Alternaria brassicae were evaluated. The results show that compound 4l and 4p, which bear only one electron-donating group on the para-position of phenyl or benzyl group, possessed excellent inhibitory activities against the above four fungi. |
| format | Article |
| id | doaj-art-abe612e226574052a4d9761febeff78d |
| institution | Kabale University |
| issn | 0973-4945 2090-9810 |
| language | English |
| publishDate | 2012-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | E-Journal of Chemistry |
| spelling | doaj-art-abe612e226574052a4d9761febeff78d2025-02-03T05:45:01ZengWileyE-Journal of Chemistry0973-49452090-98102012-01-019121121810.1155/2012/863135Synthesis and Fungicidal Activity of Pyrazolecarboxamide Containing α-Aminoacetanilide MoietyZhi-Yong Fang0Hong Jiang1Xiao-Dong Ye2Department of Chemistry, Huazhong Agricultural University, Wuhan 430070, ChinaDepartment of Chemistry, Huazhong Agricultural University, Wuhan 430070, ChinaDepartment of Chemistry, Huazhong Agricultural University, Wuhan 430070, ChinaA series of pyrazolecarboxamides containing α-aminoacetanilide moiety (4) were synthesized. These compounds were characterized by IR, MS and 1H NMR. Their fugicidal activities against Rhizoctonia solani, Sclerotinia sclerotiorum, Monilinia fructicola and Alternaria brassicae were evaluated. The results show that compound 4l and 4p, which bear only one electron-donating group on the para-position of phenyl or benzyl group, possessed excellent inhibitory activities against the above four fungi.http://dx.doi.org/10.1155/2012/863135 |
| spellingShingle | Zhi-Yong Fang Hong Jiang Xiao-Dong Ye Synthesis and Fungicidal Activity of Pyrazolecarboxamide Containing α-Aminoacetanilide Moiety E-Journal of Chemistry |
| title | Synthesis and Fungicidal Activity of Pyrazolecarboxamide Containing α-Aminoacetanilide Moiety |
| title_full | Synthesis and Fungicidal Activity of Pyrazolecarboxamide Containing α-Aminoacetanilide Moiety |
| title_fullStr | Synthesis and Fungicidal Activity of Pyrazolecarboxamide Containing α-Aminoacetanilide Moiety |
| title_full_unstemmed | Synthesis and Fungicidal Activity of Pyrazolecarboxamide Containing α-Aminoacetanilide Moiety |
| title_short | Synthesis and Fungicidal Activity of Pyrazolecarboxamide Containing α-Aminoacetanilide Moiety |
| title_sort | synthesis and fungicidal activity of pyrazolecarboxamide containing α aminoacetanilide moiety |
| url | http://dx.doi.org/10.1155/2012/863135 |
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