1974
DOI: 10.1002/anie.197402061
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A Simple Synthesis of 3(5)‐Aminopyrazole

Abstract: ethoxycarbonylaza[l3]annulenes (1) [41.Photolysis of the addition product of ethoxycarbonylnitrene to tricyclo- [8.6.O.O2v9] hexadeca-3,5,7,11,13,15-hexaene leads to three isomeric N-ethoxycarbonylaza[ 17lannulenes (4) ['I. Treatment of the azaannulenes ( I ) and ( 4 ) respectively with potassium tert-butoxide in T H F at 0°C alway furnishes the same aza[ 133-and am[ 17lannulenyl anions, according to NMR spectroscopic evidence. On the basis of the NMR spectra (see Table 1) and double resonance experiments con… Show more

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Cited by 17 publications
(2 citation statements)
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“…Thus, either 21 does not the pyrazole -* imidazole phototransposition. 3-Phenyl-2-(Ñ-phenylimmo)-2H-azirine(32…”
mentioning
confidence: 99%
“…Thus, either 21 does not the pyrazole -* imidazole phototransposition. 3-Phenyl-2-(Ñ-phenylimmo)-2H-azirine(32…”
mentioning
confidence: 99%
“…Both authors on reconducting the above reaction have shown that it affords a mixture of two isomeric pyrazoles (53% and 27%) [146], (47% and 8%) [147]. These author have shown on the basis of chemical evidences as well as spectroscopic data that the major product for which the 3-amino-4,5-dicyano-1-methylpyrazole structure was formally assigned is really 1-methyl-3,4-dicyano-5-aminopyrazole.…”
Section: Scheme 35mentioning
confidence: 96%