Detalhes bibliográficos
Ano de defesa: |
2006 |
Autor(a) principal: |
Castral, Thaís Corrêa |
Orientador(a): |
Corrêa, Arlene Gonçalves
 |
Banca de defesa: |
Não Informado pela instituição |
Tipo de documento: |
Dissertação
|
Tipo de acesso: |
Acesso aberto |
Idioma: |
por |
Instituição de defesa: |
Universidade Federal de São Carlos
|
Programa de Pós-Graduação: |
Programa de Pós-Graduação em Química - PPGQ
|
Departamento: |
Não Informado pela instituição
|
País: |
BR
|
Palavras-chave em Português: |
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Área do conhecimento CNPq: |
|
Link de acesso: |
https://repositorio.ufscar.br/handle/20.500.14289/6408
|
Resumo: |
The present study describes the preparation of amides containing the methylenedioxyphenyl group and also their activity against the leaf-cutting ant, Atta sexdens rubropilosa, its symbiotic fungus Leucoagaricus gongylophorus and the fall armyworm, Spodoptera frugiperda, larvae. From the bioassays it was observed that N-piperidine-3-(3 ,4 - methylenedioxyphenyl)-2-(E)-propenamide (65) was the most promising as insecticide agent among the compounds studied against S. frugiperda with an LD50=1.07 µg/mg larvae. Amide 65 and N,N-diethyl-3-(3 ,4 - methylenedioxyphenyl)-2-(E)-propenamide (66) were the most active against the symbiotic fungus; and N-pirrolidine-3-(3 ,4 -methylenedioxyphenyl)-2-(E)- propenamide (67) and N-benzyl-3-(3 ,4 -methylenedioxyphenyl)-2-(E)- propenamide (72) against the leaf-cutting ant. Additional studies were necessary to establish the structure activity relationship for piperamides. Thus, Combinatorial Chemistry technologies were employed and a solution-phase synthesis of indexed collection of amides was carried out, identified by Gas Chromatography coupled with Mass Spectroscopy (GC/MS), and screened against S. frugiperda. From this library, the most active compound identified was 1-[4- (trifluoromethoxy)benzoyl]piperidine, A8B1, which was then individually synthesized and evaluated. It has shown a LD50 = 8,15 µg/mg larvae, thus less active than amide 65 against S. frugiperda. |