658081-82-4Relevant articles and documents
Functionalization reactions of various pyrazole-3-carboxylic acid chlorides with some ureas
Ilhan, Ilhan ?zer,Demirkol, Kazim,?nal, Zülbiye,Akko?, Senem,?adir, Mehmet
, p. 2365 - 2368 (2014/06/09)
The 1H-pyrazole-3-carboxylic acids 2 or their remarkably stable acid chlorides 3 can easily be converted into the corresponding 1Hpyrazole- 3-carbonyl-N'-urea derivatives (5a-k) from reaction with urea nucleophiles. It has been demonstrated that with the
Reactions of some pyrazole-3-carboxylic acid and carboxylic acid chlorides with various alcohols
Ilhan, Ilhan ?zer,Bahadir, ?zlem,?nal, Zülbiye,Saripinar, Emin
scheme or table, p. 141 - 144 (2012/08/08)
The reactions of 4-benzoyl-1-(2,4-dinitrophenyl)-5-phenyl-1 H-pyrazole-3-carboxylic acid (2b), 4-benzoyl-1-(4-nitrophenyl)-5-phenyl-1 H-pyrazole-3-carboxylic acid chloride (3a) and 4-benzoyl-1-(2,4-dinitrophenyl)- 5-phenyl-1 H-pyrazole-3-carboxylic acid c
Studies on reactions of cyclic oxalyl compounds with hydrazines or hydrazones. 2. Synthesis and reactions of 4-benzoyl-1-(4-nitrophenyl)-5-phenyl- 1H-pyrazole-3-carboxylic acid
Sener,Kasimogullari,Sener,Genc
, p. 1039 - 1046 (2007/10/03)
4-Benzoyl-1-(4-nitrophenyl)-5-phenyl-1H-pyrazole-3-carboxylic acid, obtained from the corresponding furan-2,3-dione and N-benzylidene-N'-(4- nitrophenyl)hydrazine, was converted via reactions of its acid chloride with various alcohols or N-nucleophiles in