Terpenic olefin epoxidation using metals acetylacetonates as catalysts
Identifieur interne : 000F81 ( Main/Exploration ); précédent : 000F80; suivant : 000F82Terpenic olefin epoxidation using metals acetylacetonates as catalysts
Auteurs : Naima Fdil [Maroc] ; Abderrahmane Romane [Maroc] ; Smail Allaoud [Maroc] ; Abdallah Karim [Maroc] ; Yves Castanet [France] ; André Mortreux [France]Source :
- Journal of Molecular Catalysis A: Chemical [ 1381-1169 ] ; 1996.
Abstract
Efficient epoxidation of natural terpenic olefins is performed using nickel acetylacetonate, oxygen and a branched aldehyde at ambient temperature. Total conversions are achieved with selectivities up to 90% into epoxide. Under the same conditions other catalytic systems using transition metal acetylacetonates (Mn(acac)n) have been used, some of which also gave satisfactory results.
Url:
DOI: 10.1016/1381-1169(95)00284-7
Affiliations:
- France, Maroc
- Hauts-de-France, Marrakech-Tensift-Al Haouz, Nord-Pas-de-Calais
- Marrakech, Villeneuve D'Ascq
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- to stream Istex, to step Corpus: 000998
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- to stream Istex, to step Checkpoint: 000822
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Efficient epoxidation of natural terpenic olefins is performed using nickel acetylacetonate, oxygen and a branched aldehyde at ambient temperature. Total conversions are achieved with selectivities up to 90% into epoxide. Under the same conditions other catalytic systems using transition metal acetylacetonates (Mn(acac)n) have been used, some of which also gave satisfactory results.</div>
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