textjournal article
Design, Multicomponent Synthesis, and Bioactivities of Novel Neonicotinoid Analogues with 1,4-Dihydropyridine Scaffold
Abstract
Novel neonicotinoid analogues bearing a 1,4-dihydropridine scaffold were designed and synthesized by multicomponent reactions (MCRs) to enhance π−π stacking. The synthesized compounds were identified by 1H NMR, 13C NMR, high-resolution mass spectroscopy, and elemental analysis. Bioassay tests showed that some of them exhibited high insecticidal activities against pea aphid (Aphis craccivora)- Text
- Journal contribution
- Biochemistry
- Neuroscience
- Sociology
- Chemical Sciences not elsewhere classified
- Multicomponent Synthesis
- analysis
- analogue
- mass spectroscopy
- insecticidal activities
- Bioactivitie
- scaffold
- 13 C NMR
- 1 H NMR
- multicomponent reactions
- pea aphid
- Novel Neonicotinoid Analogues
- ScaffoldNovel
- Aphis craccivora
- dihydropridine
- Bioassay tests
- compound
- neonicotinoid
- Dihydropyridine
- MCR
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Last time updated on 16/03/2018
This paper was published in The Francis Crick Institute.
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