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Título : | Coupling of monoterpenic alkenes and alcohols with benzaldehyde catalyzed by silica-supported tungstophosphoric heteropoly acid. |
Autor : | Cotta, Rafaela Ferreira Rocha, Kelly Alessandra da Silva Kozhevnikova, Elena Fedorovna Kozhevnikov, Ivan V. Gusevskaya, Elena Vitalievna |
Palabras clave : | Biomass-based feedstock Heteropoly acid Cycloaddition Acid catalysis |
Fecha de publicación : | 2017 |
Citación : | COTTA, R. F. et al. Coupling of monoterpenic alkenes and alcohols with benzaldehyde catalyzed by silica-supported tungstophosphoric heteropoly acid. Catalysis Today, v. 289, p. 14-19, jul. 2017. Disponível em: <https://www.sciencedirect.com/science/article/pii/S0920586116304874>. Acesso em: 05 abr. 2018. |
Resumen : | The reactions of biomass-based substrates, i.e., limonene, -pinene, -pinene, terpinolene, -terpineol,nerol and linalool, with benzaldehyde in the presence of tungstophosphoric heteropoly acid H3PW12O40(HPW) supported on silica give an oxabicyclo[3.3.1]nonene compound with fragrance characteristics ingood to excellent yields. The reactions apparently involve the formation of -terpenyl carbenium ion bythe protonation of alkene or dehydration of alcohol followed by the nucleophilic attack of benzaldehyde.The subsequent oxonium-ene cyclization of the resulting oxocarbenium ion gives the oxabicyclic product.The process is an environmentally benign and heterogeneous and can be performed under mild conditionswith low catalyst amounts and no significant leaching of active components. |
URI : | http://www.repositorio.ufop.br/handle/123456789/9959 |
metadata.dc.identifier.uri2: | https://www.sciencedirect.com/science/article/pii/S0920586116304874 |
ISSN : | 09205861 |
Aparece en las colecciones: | DEQUI - Artigos publicados em periódicos |
Ficheros en este ítem:
Fichero | Descripción | Tamaño | Formato | |
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ARTIGO_CouplingMonoterpenicAlkenes.pdf Restricted Access | 385,72 kB | Adobe PDF | Visualizar/Abrir |
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