Chromatographic separation of isomeric forms of a tetradentate schiff base derived from 1,1,1-trifluoro-5,5-dimethylhexane-2,4-dione and 1,2-diaminoethane
Autor: | Sergio Dilli, Emilios Patsalides |
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Rok vydání: | 1977 |
Předmět: | |
Zdroj: | Journal of Chromatography A. 134:477-482 |
ISSN: | 0021-9673 |
DOI: | 10.1016/s0021-9673(00)88547-7 |
Popis: | Reaction between the asymmetrical β-diketone 1,1,1-trifluoro-5,5-dimethylhexane-2,4-dione with 1,2-diaminoethane gives, among other products, two distinct tetradentate ketoenamine isomers. These compounds have been separated chromatographically from the numerous reaction products and identified. The major product of the reaction was the dihydrodiazepin derivative. Some properties of the isomers are given. |
Databáze: | OpenAIRE |
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