| Synthesis and acaricidal activity of strobilurin-pyrimidine derivatives | |
| Alternative Title | Synthesis and acaricidal activity of strobilurin-pyrimidine derivatives |
| Chai BaoShan1; Liu ChangLing2; Li HuiChao2; Liu ShaoWu2; Xu Ying2; Song YuQuan2; Chang JunBiao1 | |
| 2014 | |
| Source Publication | CHINESE CHEMICAL LETTERS
 |
| ISSN | 1001-8417 |
| Volume | 25Issue:1Pages:137-140 |
| Abstract | Pyriminostrobin, a new acaricide, was discovered in our previous studies. Because introducing fluorine into organic compounds can increase bioactivity, pyriminostrobin was modified as a series of strobilurin-pyrimidine derivatives for biological screening. The compounds were characterized by H-1 NMR, MS and elemental analysis. Preliminary bioassays demonstrated that compounds 7e and 7i exhibited significant control against Tetranychus cinnabarinus (Boisd.) at 0.625 mg L-1, and their acaricidal potencies were higher than pyriminostrobin in a greenhouse. The relationship between structure and acaricidal activity was also studied. (C) 2013 Chang-Ling Liu and Jun-Biao Chang. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved. |
| Other Abstract | Pyriminostrobin, a new acaricide, was discovered in our previous studies. Because introducing fluorine into organic compounds can increase bioactivity, pyriminostrobin was modified as a series of strobilurin-pyrimidine derivatives for biological screening. The compounds were characterized by~1H NMR, MS and elemental analysis. Preliminary bioassays demonstrated that compounds 7e and 7i exhibited significant control against Tetranychus cinnabarinus (Boisd.) at 0.625 mg L~(-10, and their acaricidal potencies were higher than pyriminostrobin in a greenhouse. The relationship between structure and acaricidal activity was also studied. |
| Keyword | Strobilurin-pyrimidine Acaricidal activity Intermediate derivatization method Pyriminostrobin |
| Indexed By | CSCD |
| Language | 英语 |
| Funding Project | [National Natural Science Foundation of China] ; [NSFC] ; [Outstanding Scholar Foundation of Henan Province] ; [National Key Basic Research Program of China (973 Program)] ; [National Key Technology Support Program] |
| CSCD ID | CSCD:5050814 |
| Citation statistics |
Cited Times:3[CSCD]
[CSCD Record]
|
| Document Type | 期刊论文 |
| Identifier | http://ir.imr.ac.cn/handle/321006/155794 |
| Collection | 中国科学院金属研究所 |
| Affiliation | 1.郑州大学 2.中国科学院金属研究所 |
| Recommended Citation GB/T 7714 | Chai BaoShan,Liu ChangLing,Li HuiChao,et al. Synthesis and acaricidal activity of strobilurin-pyrimidine derivatives[J]. CHINESE CHEMICAL LETTERS,2014,25(1):137-140. |
| APA | Chai BaoShan.,Liu ChangLing.,Li HuiChao.,Liu ShaoWu.,Xu Ying.,...&Chang JunBiao.(2014).Synthesis and acaricidal activity of strobilurin-pyrimidine derivatives.CHINESE CHEMICAL LETTERS,25(1),137-140. |
| MLA | Chai BaoShan,et al."Synthesis and acaricidal activity of strobilurin-pyrimidine derivatives".CHINESE CHEMICAL LETTERS 25.1(2014):137-140. |
| Files in This Item: | There are no files associated with this item. | |||||
Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.
Edit Comment