2011
DOI: 10.1007/s00044-011-9602-8
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Chalcones as promising pesticidal agents against diamondback moth (Plutella xylostella): microwave-assisted synthesis and structure–activity relationship

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Cited by 23 publications
(17 citation statements)
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“…38 Desta mesma forma, foram demonstrados eventuais novas aplicações de chalconas na proteção de cultivos e pesticidas orgânicos e para controle de plantas daninhas. 39 Em vista disto, foram ultilizados estudos de análise quantitativa da relação estrutura-atividade em uma série de chalconas e esses mostraram que grupos substituintes retiradores de elétrons, no anel cetônico, geram bons agentes pesticidas 40 . A Figura 4 apresenta estruturas de chalconas e análogos de chalconas.…”
Section: Inovação Na Perceptiva Ambientalunclassified
“…38 Desta mesma forma, foram demonstrados eventuais novas aplicações de chalconas na proteção de cultivos e pesticidas orgânicos e para controle de plantas daninhas. 39 Em vista disto, foram ultilizados estudos de análise quantitativa da relação estrutura-atividade em uma série de chalconas e esses mostraram que grupos substituintes retiradores de elétrons, no anel cetônico, geram bons agentes pesticidas 40 . A Figura 4 apresenta estruturas de chalconas e análogos de chalconas.…”
Section: Inovação Na Perceptiva Ambientalunclassified
“…The effectiveness of chalcones is enhanced by the presence of electron-withdrawing substituents in ring A and electron-withdrawing or electron-releasing substituents in ring B. A group of synthetic chalcones has been found to be insecticidal against Plutella xylostella, which is considered one of the most destructive pests of crucifers worldwide (Kumar et al, 2012). The naturally-occurring chalcones lonchocarpin, derricin, derricidin and isocordoin, isolated from Lonchocarpus neuroscapha, showed deterrent activity against larvae of Spodoptera littoralis and S. exempta (Simmonds et al, 1990), which are pests able to destroy crops rapidly.…”
Section: Nematicides Insect Deterrents and Antifeedantsmentioning
confidence: 99%
“…Chalcones, members of the flavonoid class of secondary metabolites, are composed of two aromatic ring moieties linked by an α,β‐unsaturated ketone, [23] and are obtained from the leaves, stems, roots and flowers of plants [24] . Additionally, chalcones can be readily synthetized through a wide array of methodologies, [25] providing easy access to a broad structural diversity, and thus affording a variety of biological activities, [26] as anti‐inflammatory, [27,28] antitumoral, [29] antiviral, [30] insecticide, [31,32] nematicide, [33] larvicide [34,35] and herbicide [36,37] . Due to their potent capacity to scavenge reactive oxygen species as well as the electrophilic nature of the α,β‐unsaturated ketone moiety, chalcones have also been used as antioxidant agents [38–40] .…”
Section: Introductionmentioning
confidence: 99%