Zobrazeno 1 - 10 of 17 pro vyhledávání: '"Jueping Ni"'
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Optimization, Structure–Activity Relationship, and Mode of Action of Nortopsentin Analogues Containing Thiazole and Oxazole Moieties
Autor: Jueping Ni, Yanan Hao, Yongqiang Li, Jincheng Guo, Huailin Pang, Xiaofei Ji, Ziwen Wang, Dejun Ma, Yuxiu Liu, Qingmin Wang
Publikováno v: Journal of Agricultural and Food Chemistry. 67:10018-10031
Plant diseases seriously endanger plant health, and it is very difficult to control them. A series of nortopsentin analogues were designed, synthesized, and evaluated for their antiviral activities and fungicidal activities. Most of these compounds d
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8fe5ce6a039b19516d7bb90de0e5f08
https://doi.org/10.1021/acs.jafc.9b04093
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3
Synthesis, insecticidal activities and structure-activity relationship studies of novel anthranilic diamides containing pyridylpyrazole-4-carboxamide
Autor: Qi Liu, Kai Chen, Jueping Ni, Yufeng Li, Hongjun Zhu, Qiang Wang
Publikováno v: Pest Management Science. 71:1503-1512
BACKGROUND Anthranilic diamide insecticides containing pyridylpyrazole-5-carboxamide are extremely important in modern agriculture. New structurally modified compounds with high insecticidal activity were discovered by designing a series of novel pyr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27c14241c9733f7f69ffd4990d2876c0
https://doi.org/10.1002/ps.3954
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5
Synthesis, insecticidal activity, structure–activity relationship (SAR) and density functional theory (DFT) of novel anthranilic diamides analogs containing 1,3,4-oxadiazole rings
Autor: Jueping Ni, Qiang Wang, Hongjun Zhu, Ding Yuan, Yufeng Li, Kai Chen, Qi Liu
Publikováno v: RSC Adv.. 4:55445-55451
A series of anthranilic diamides analogs (5a–x) containing 1,3,4-oxadiazole rings were synthesized and characterized by 1H NMR, 13C NMR and mass spectrometry. The structure of N-(4-chloro-2-methyl-6-(5-(thiophen-2-yl)-1,3,4-oxadiazol-2-yl)phenyl)me
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::dec7645a55f2b252ddd3f25da1d39539
https://doi.org/10.1039/c4ra06356b
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7
Design, synthesis, insecticidal activity and structure-activity relationship of 3,3-dichloro-2-propenyloxy-containing phthalic acid diamide structures
Autor: Mei-Li Feng, Hongjun Zhu, Liang Zhao, Bin-Bin Xi, Yufeng Li, Jueping Ni
Publikováno v: Pest Management Science. 68:986-994
BACKGROUND: Phthalic acid diamide derivatives are among the most important classes of synthetic insecticides. In this study, a 3,3-dichloro-2-propenyloxy group, the essential active group of pyridalyl derivatives, was incorporated into phthalic acid
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::662682d94189467ffe5a241814d1c62c
https://doi.org/10.1002/ps.3243
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8
Soil microbial degradation of neonicotinoid insecticides imidacloprid, acetamiprid, thiacloprid and imidaclothiz and its effect on the persistence of bioefficacy against horsebean aphid Aphis craccivora Koch after soil application
Autor: Yuyu Gu, Hua Wei, Guodong Huang, Sheng Yuan, Yi-Jun Dai, Jueping Ni, Zhonghua Liu
Publikováno v: Pest Management Science. 67:1245-1252
BACKGROUND: The neonicotinoids imidacloprid, imidaclothiz, acetamiprid and thiacloprid consist of similar structural substituents but differ considerably with respect to soil use. Therefore, the effects of soil microbial activity on the degradation a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9051e0994cb9f472fb31878e3b797b0
https://doi.org/10.1002/ps.2174
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9
Biotransformation of thianicotinyl neonicotinoid insecticides: Diverse molecular substituents response to metabolism by bacterium Stenotrophomonas maltophilia CGMCC 1.1788
Autor: Wei-Wei Ji, Sheng Yuan, Yi-Jun Dai, Jueping Ni, Cigang Yu, Wenping Xu, Wenjian Zhang, Yin-Juan Zhao
Publikováno v: Bioresource Technology. 101:3838-3843
The carbon atom that neighbors the tertiary amine attached to the 6-chloro-3-pyridinylmethyl moiety is the key active site in the hydroxylation of the neonicotinoids imidacloprid and thiacloprid as well as in the demethylation of acetamiprid by Steno
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46fecc9318b5acc2555c163469cee9ca
https://doi.org/10.1016/j.biortech.2010.01.069
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10
Hydroxylation of thiacloprid by bacterium Stenotrophomonas maltophilia CGMCC1.1788
Autor: Jueping Ni, Cigang Yu, Jun Luo, Sheng Yuan, Yin-Juan Zhao, Wenping Xu, Yi-Jun Dai
Publikováno v: Biodegradation. 20:761-768
Chloropyridinyl neonicotinoid insecticides play a major role in crop protection and flea control on cats and dogs. Imidacloprid, thiacloprid and acetamiprid have in common the 6-chloro-3-pyridinylmethyl group but differ in the nitroguanidine or cyano
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69a059c1ede00b83e1a953ef41e54e22
https://doi.org/10.1007/s10532-009-9264-0
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