Synthesis and anti-aphid Aphis gossypii Glover activity of some new Quinoline derivatives

• Autorzy: Aly M.R.E. , El-Mageed A. E. M. , Kafafy A. K. M. , Nawwar G. A. M.

Warianty tytułu

PL

Synteza nowych pochodnych związków guinoliny i ich aktywność przeciwko Ahpis gossypii (Glover)

• Języki publikacji: EN

Abstrakty

EN

A series of quinoline derivatives have been elaborated from reaction of 2-(m- and p-acetylanilino)-quinolines 6a-b with aldehydes under Claisen-Schmidt conditions followed by cyclization with phenyl hydrazine and hydroxylamine. Reaction of 6a and 6b with hydrazine, semicarbazide and thiosemicarbazide, cyanoacetylhydrazide and some subsequent condensation reactions led to diverse quinoline derivatives. Anti-Aphid Aphis gossypii that harm cotton crop in Egypt was screened. Compound 12 showed an LC50 value of 19429E-10 ppm which is much more active than Marshal (Carbosulfan), one of the broad spectrum insecticides widely used in this field.

PL

Opracowano serię pochodnych związków quinoliny w wyniku reakcji 2-(m i p-acetylanilino)-quinolin 6a-b z aldehydami według Clainsen-Schmidt'a, a następnie poprzez cyklizację z fenylohydrazyną i hydroksyloaminą. Reakcja 6a i 6b z hydrazyną, semikarbazydem i tiosemikarbazydem, cyjanoacetylohydrazydem oraz kolejne reakcje kondensacji doprowadziły do powstania pochodnych związków quinoliny. Przedmiotem badań była ocena ich skuteczności przeciwko mszycy Apis gossypii, szkodnikowi upraw bawełny w Egipcie. Komponent 12 o wartości LC50 dla 19429E-10 ppm okazał się bardziej skuteczny niż preparat Marchal (karbosulfan), jeden z powszechnie stosowanych insektycydów w zwalczaniu A. gossypii.

• Wydawca: -
• Czasopismo: Journal of Plant Protection Research
• Rocznik: 2011
• Tom: 51
• Numer: 2
• Opis fizyczny: p.114-120,fog.,ref.

Twórcy

autor

Aly M.R.E.

• Chemistry Department, Faculty of Science, Port Said University 42523, Egypt

autor

El-Mageed A. E. M.

autor

Kafafy A. K. M.

autor

Nawwar G. A. M.

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