130774-70-8Relevant academic research and scientific papers
Lipoxygenase inhibitors, IV: Synthesis and cyclization reactions of open-chain N1-aryl-substituted amidrazones
Frohberg,Kupfer,Stenger,Baumeister,Nuhn
, p. 505 - 516 (2007/10/02)
α-Carbonyl carboxylic acid arylhydrazonochlorides obtained by Japp-Klingemann reaction are the starting substances for the synthesis of α-carbonyl carboxylic acid arylhydrazonoamides, -esters and -thioesters. The inhibiting activity of these compounds against 15- and 5-lipoxygenase is described. Reactions of derivatives of amidrazones with formaldehyde give triazole, triazoline and unexpected benzotriazepine derivatives.
SYNTHESIS AND REACTIONS OF TRIPHENYLPHOSPHONIMINOGLYOXALIC ACID ANILIDE ARYLHYDRAZONES
Shawali, Ahmed S.,Hassaneen, Hamdi M.,Fahmy, Abdelgawad A.,Abunada, Nada M.,Mousa, Hiyam A. H.
, p. 259 - 265 (2007/10/02)
A series of α-azidoglyoxalic acid anilide arylhydrazones 2 were prepared and converted to the corresponding phosphonimines 6 by reaction with triphenylphosphine.Treatment of the latter with acyl chlorides yielded the phosphonium salts 9 which afforded, up
