Síntese de novos azóis derivados da 1,1- difenilacetona

• Ano de defesa: 2014
• Autor(a) principal: Friedein, Alynne Alegre Souto
• Tipo de documento: Dissertação
• Tipo de acesso: Acesso aberto
• dARK ID: ark:/26339/001300000r007
• Idioma: por
• Instituição de defesa: Universidade Federal de Santa Maria; BR; Química; UFSM; Programa de Pós-Graduação em Química
• Palavras-chave em Português: β-alcoxivinil cetonas; Isoxazóis; Pirazóis; β-alcoxivinil ketones; Isoxazoles; Pyrazoles; CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
• Link de acesso: http://repositorio.ufsm.br/handle/1/10591

This work describes an efficient method to obtaining new heterocycles from the reaction of acetalization of the ketonic carbonyl, followed by acylation of the enolether, generated in situ from the acetal derivative of 1,1-diphenylacetone, with trifluoroacetic anhydride, tricloroacetila of chloride, clorodiflúoracético anhydride, pentaflúorpropiônico anhydride in the absence of solvents. There were performed reactions of cyclocondensation between 1,1,1-trialo-4-alkoxy-3-alquen-2-ones and hydroxylamine hydrochloride, forming, in general, the 5-trialometil-5-hydroxy-4,5-diidroisoxazóis. To obtaining pyrazoline compounds, was proposed the cyclocondensation between the β-ketones alcoxivinil (ou é β-alcoxivinil ketones?) and four different dinucleophiles: monohydrate hydrazine, phenylhydrazine, thiosemicarbazide and aminoguanidine carbonate. All compounds synthesized on this work, since the acetal to the final heterocycles are inedited and their structures were confirmed by RMN 1H e 13C data. In this work, were also performed antimicrobial activity tests of some compounds against microorganisms, wherein some showed significant result for bacteria of great clinical interest, Staphylococcus aureus.