1973
DOI: 10.1007/bf00910055
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Synthesen und Reaktionen von Pyridazinderivaten, 3. Mitt.

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Cited by 20 publications
(4 citation statements)
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“…The 1 H NMR spectra of the oximes of pyridazine [124][125][126], pyrimidine [11,[126][127][128][129], pyrazine [124], quinoxaline [130], 1,3,4-triazine [68], and 1,3,4-thiadiazine [120] have been investigated in greatest detail.…”
Section: Structurementioning
confidence: 99%
See 1 more Smart Citation
“…The 1 H NMR spectra of the oximes of pyridazine [124][125][126], pyrimidine [11,[126][127][128][129], pyrazine [124], quinoxaline [130], 1,3,4-triazine [68], and 1,3,4-thiadiazine [120] have been investigated in greatest detail.…”
Section: Structurementioning
confidence: 99%
“…IR spectroscopy was also used to study the structure of pyridazine [124], pyrimidine [11], quinazoline [127], quinoxaline [130], and 1,2,4-triazole [67] oximes. In the IR spectrum of 2-pyrimidine aldoxime there is a band for the free OH group at 3600 cm −1 .…”
Section: Structurementioning
confidence: 99%
“…3,6-Dichloropyridazine-4-carboxylic acid chloride 3 was prepared from 3,6-dichloro-4-pyridazinecarboxylic acid with SOCI 2 (Ried and Eichhorn, 1988); 3,6-dichloropyridazine-4-carboxylic acid was available from 3,6-dichloro-4-methylpyridazine via oxidationwith K 2Cr2 0 7 (Heinisch, 1973).…”
Section: Starting Materialsmentioning
confidence: 99%
“…Starting materials 3,6-Dichloropyridazine-4-carboxylic acid chloride was prepared from 3,6-dichloropyridazine-4-carboxylic acid with SOC1 2 (Ried & Eichhorn, 1988); 3,6-dichloropyridazine-4-carboxylic acid was available from 3,6-dichloro-4-methylpyridazine via oxidation with~Cr207 (Heinisch, 1973). 3,6-Dichloro-N-(2-fluoro-5-methylphenyl)-pyridazine-4-carboxamide (3a) was prepared from 3,6dichloropyridazine-4-carboxylic acid chloride and 2-fluoroaniline (Heinisch et al, 1997a).…”
Section: Introductionmentioning
confidence: 99%