1978
DOI: 10.1002/chin.197811325
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ChemInform Abstract: 1,6,11,16‐TETRAAZAPORPHYRINOGEN, SYNTHESIS AND BEHAVIOR

Abstract: Die aus den Chlormethylpyrazolen (I) hergestellten Hydrazine (II) werden mit den β‐Diketonen (III) zu Gemischen der Verbindungen (IV) und (V) umgesetzt.

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Cited by 12 publications
(12 citation statements)
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“…(1.5-Dimethyl-1H-pyrazol-3-yl) methanol [62,63] (1.2 g, 9.52 mmol) was dissolved in 1,4-dioxane (100 mL). Activated manganese dioxide (21.88 g) was added to the solution and the suspension was stirred under reflux for 5 h. The reaction was monitored by TLC (alumina, CH 2 Cl 2 as eluent).…”
Section: Methodsmentioning
confidence: 99%
“…(1.5-Dimethyl-1H-pyrazol-3-yl) methanol [62,63] (1.2 g, 9.52 mmol) was dissolved in 1,4-dioxane (100 mL). Activated manganese dioxide (21.88 g) was added to the solution and the suspension was stirred under reflux for 5 h. The reaction was monitored by TLC (alumina, CH 2 Cl 2 as eluent).…”
Section: Methodsmentioning
confidence: 99%
“…23 Alkylation of compound 2 with ethylbromoacetate in THF was carried out under solid-liquid phase transfer catalysis to favour the -isomer. 27 Thus, one isolated major product 3 as the -isomer was formed in 20% yield. The second positional isomer 4 was also isolated but with a very low yield (1%).…”
Section: Resultsmentioning
confidence: 99%
“…The result of our investigation was given below (Schemes 1 and 2): The preparation of the new pyrazolic acid precursors 5-8 was carried out in two steps from the pyrazolic ester 1. The preparation in good yield of one isolated major product 2-4 from 3(5)-carboxymethyl-5(3)- methylpyrazole 1 [16] has been already reported [17,18] in the literature. The second step was to hydrolyse the products 1-4 under reflux condition of NaOH followed by neutralisation with HCl to give the pyrazolic acid precursors 5-8 in good yield [19][20][21].…”
Section: Chemistrymentioning
confidence: 87%