Design, synthesis, insecticidal activity and 3D-QSR study for novel trifluoromethyl pyridine derivatives containing an 1,3,4-oxadiazole moiety
RSC Advances, ISSN: 2046-2069, Vol: 8, Issue: 12, Page: 6306-6314
2018
- 28Citations
- 18Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations28
- Citation Indexes28
- 28
- CrossRef23
- Captures18
- Readers18
- 18
Article Description
A series of trifluoromethyl pyridine derivatives containing 1,3,4-oxadiazole moiety was designed, synthesized and bio-assayed for their insecticidal activity. The result of bio-assays indicated the synthesized compounds exhibited good insecticidal activity against Mythimna separata and Plutella xylostella, most of the title compounds show 100% insecticidal activity at 500 mg L and >80% activity at 250 mg L against the two pests. Compounds E18 and E27 showed LC values of 38.5 and 30.8 mg L against Mythimna separata, respectively, which were close to that of avermectin (29.6 mg L); compounds E5, E6, E9, E10, E15, E25, E26, and E27 showed 100% activity at 250 mg L, which were better than chlorpyrifos (87%). CoMFA and CoMSIA models with good predictability were proposed, which revealed the electron-withdrawing groups with an appropriate bulk at 2- and 4-positions of benzene ring could enhance insecticidal activity.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85042043458&origin=inward; http://dx.doi.org/10.1039/c8ra00161h; http://www.ncbi.nlm.nih.gov/pubmed/35540384; https://xlink.rsc.org/?DOI=C8RA00161H; https://dx.doi.org/10.1039/c8ra00161h; https://pubs.rsc.org/en/content/articlelanding/2018/ra/c8ra00161h
Royal Society of Chemistry (RSC)
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