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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kumar, Dalip | - |
dc.date.accessioned | 2021-10-27T04:23:34Z | - |
dc.date.available | 2021-10-27T04:23:34Z | - |
dc.date.issued | 2000-08 | - |
dc.identifier.uri | https://cdnsciencepub.com/doi/abs/10.1139/v00-104?journalCode=cjc | - |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3093 | - |
dc.description.abstract | The reaction between aryl or heteroarylhydrazines with fluorinated β-diketones (CF3COCH2COR) yields a variety of 3-, 5-, and 3,5-trifluoromethylpyrazoles and 5-trifluoromethyl-5-hydroxy-Δ2-pyrazolines. Twenty-one of such compounds have been isolated and identified by 13C and 19F NMR. Together with the results from the literature they provide a comprehensive overview of the reaction. Semi-empirical calculations at the PM3 level have been used to rationalize these results. The outcome that emerges seems to be that the dehydration of a pair of 3,5-dihydroxypyrazolidines kinetically controls the isomer formed.Key words: hydrazines, 1,3-diketones, pyrazolines, pyrazoles, PM3 calculations. | en_US |
dc.language.iso | en | en_US |
dc.publisher | CSP | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Hydrazines | en_US |
dc.subject | β-dicarbonyl compounds | en_US |
dc.title | The reaction between hydrazines and β-dicarbonyl compounds: proposal for a mechanism | en_US |
dc.type | Article | en_US |
Appears in Collections: | Department of Chemistry |
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