2013
DOI: 10.5155/eurjchem.4.2.102-109.723
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Regioselective synthesis of some functionalized 3,4’-bis-(pyrazolyl)ketones and chemoselectivity in their reaction with hydrazine hydrate

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Cited by 10 publications
(4 citation statements)
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“…Condensation of 3-acetylpyrazole derivative 28 with DMF-DMA in refluxing dioxane yielded the enaminone 41. Treatment of the enaminone 41 with various hydrazonoyl halides 4a-c in refluxing dioxane in the presence of triethylamine furnished the corresponding 3,4 0 -bis-pyrazoles 42-44 (Scheme 17) [80].…”
Section: Severalmentioning
confidence: 99%
See 1 more Smart Citation
“…Condensation of 3-acetylpyrazole derivative 28 with DMF-DMA in refluxing dioxane yielded the enaminone 41. Treatment of the enaminone 41 with various hydrazonoyl halides 4a-c in refluxing dioxane in the presence of triethylamine furnished the corresponding 3,4 0 -bis-pyrazoles 42-44 (Scheme 17) [80].…”
Section: Severalmentioning
confidence: 99%
“…Heating 3-acetylpyrazole derivative 28 with hydrazine hydrate in ethanol under reflux gave the pyrazolo [3,4-d]pyridazinone derivative 67a (Scheme 28) [80].…”
Section: Severalmentioning
confidence: 99%
“…The interest in such bis -heterocycles is due to the fact that many of them exhibit more potent biological activities than the monoheterocyclic analogues [7] , [8] , [9] , [10] , [11] , [12] , [13] . In addition, many bis -pyrazole [14] , [15] , [16] , [17] and bis -1,3,4-thiadiazole [18] , [19] , [20] derivatives were reported to exhibit various pharmaceutical, agrochemical and many other applications including antibacterial, fungicidal, tuberculostatic, antiamoebic, and plant growth regulative properties [21] .…”
Section: Introductionmentioning
confidence: 99%
“…These reactions are often carried out on dipolarophiles whose stereochemistry is often not given [14][15][16][17][18][19][20].…”
Section: Introductionmentioning
confidence: 99%