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Synthesis and acaricidal activity of strobilurin-pyrimidine derivatives
Alternative TitleSynthesis and acaricidal activity of strobilurin-pyrimidine derivatives
Chai BaoShan1; Liu ChangLing2; Li HuiChao2; Liu ShaoWu2; Xu Ying2; Song YuQuan2; Chang JunBiao1
2014
Source PublicationCHINESE CHEMICAL LETTERS
ISSN1001-8417
Volume25Issue:1Pages:137-140
AbstractPyriminostrobin, 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 AbstractPyriminostrobin, 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.
KeywordStrobilurin-pyrimidine Acaricidal activity Intermediate derivatization method Pyriminostrobin
Indexed ByCSCD
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 IDCSCD:5050814
Citation statistics
Cited Times:2[CSCD]   [CSCD Record]
Document Type期刊论文
Identifierhttp://ir.imr.ac.cn/handle/321006/155794
Collection中国科学院金属研究所
Affiliation1.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.
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