5335-36-4Relevant articles and documents
Reaction of (chloro carbonyl) phenyl ketene with 5-amino pyrazolones: Synthesis, characterization and theoretical studies of 7-hydroxy-6-phenyl-3-(phenyldiazenyl)pyrazolo[1,5-a]pyrimidine-2,5(1H,4H)-dione derivatives
Zahedifar, Mahboobeh,Razavi, Razieh,Sheibani, Hassan
, p. 730 - 735 (2016/07/26)
New 7-hydroxy-6-phenyl-3-(phenyldiazenyl)pyrazolo[1,5-a]pyrimidine-2,5(1H,4H)-dione derivatives were synthesized from the reaction of (chlorocarbonyl)phenyl ketene and 5-amino pyrazolones in high to excellent yields and short reaction times. Structures of
Chemoselective three component reactions of 3-aminopyrazoles, aldehydes and malononitrile: Optimize the structures and compute the energies of possible tautomers
Sheibani, Hassan,Saheb, Vahid,Rezaei, Marjan,Zahedifar, Mahboobeh
, p. 126 - 130 (2014/03/21)
A chemoselective synthesis of 7-amino-5-aryl-2-hydroxy-3- (aryldiazenylpyrazolo[1,5-α]pyrimidine-6- carbonitriles and 4-((7-amino-6-cyano-2-hydroxy-5-arylpyrazolo[1,5-α]pyrimidine-3-yl) diazenyl)benzenesulfonamides through three-component reaction of 3-am
Voltammetric Studies on Some Arylhydrazones of α-Cyano Ketones and α-Cyano Esters
Abou-Elenien, G. M.,Ismail, N. A.,Hafez, T. S.
, p. 651 - 654 (2007/10/02)
The redox characteristics of the title compounds are extensively studied using DC-, cyclic voltammetry, coulometry, and controlled potential electrolysis in benzonitrile at platinum electrodes.These compounds are oxidized in one-electron transfer process followed by deprotonation which leads to dimerization.The reduction process differs according to the nature of the compound and the electron-withdrawing power of the substituent in the α-position.They can be reduced in a single two electron or two one electron waves leading in both cases to saturation of the hydrazonic moiety.
Kinetics and mechanism of dehydrochlorination of N-aryl-C-ethoxycarbonylformohydrazidoyl chlorides
Shawali, Ahmad S.,Albar, Hassan A.
, p. 871 - 875 (2007/10/02)
The kinetics of triethylamine (TEA) catalyzed dehydrochlorination of a series of N-aryl-C-ethoxycarbonylformohydrazidoyl chlorides 1a-m have been studied under pseudo-first-order conditions in 4:1 (v/v) dioxane-water solution at 30 deg C.For all compounds