57389-73-8Relevant academic research and scientific papers
C-H bonds as ubiquitous functionality: A general approach to complex arylated pyrazoles via sequential regioselective C-arylation and N-alkylation enabled by SEM-group transposition
Goikhman, Roman,Jacques, Teresa L.,Sames, Dalibor
supporting information; experimental part, p. 3042 - 3048 (2009/09/04)
Pyrazoles are important azole heteroarenes frequently found in pharmaceuticals and protein ligands, and there has been a growing interest in newsynthetic methods for their preparation. We report the first catalytic intermolecular C-H arylation of pyrazole
FORMATION OF PYRAZOLES AND OF IMIDAZOLES FROM PHENACYL KETAL HYDRAZONES OF ALDEHYDES
Scarpetti, David,Kano, Kunio,Anselme, Jean-Pierre
, p. 1073 - 1082 (2007/10/02)
The cyclization of phenacyl ethylene ketal (pek) hydrazones of glyoxals, benzaldehyde and acetaldehyde to pyrazoles is described; in the case of the hydrazones of benzaldehyde and acetaldehyde, the corresponding imidazoles are also formed.A mechanism is suggested for the formation of the imidazoles.
4,5-DIPHENYLIMIDAZOLES FROM THE CYCLIZATION OF BENZIL N-ALKYLMONOHYDRAZONES
Collibee, William L.,Anselme, Jean-Pierre
, p. 655 - 662 (2007/10/02)
The thermal cyclization of monodisubstituted hydrazones (1) affords the corresponding N-substituted-4,5-diphenylimidazoles in good to excellent yields; possible mechanisms for this unusual cyclization are presented.
THE UNUSUAL CYCLIZATION OF BENZIL MONOHYDRAZONES TO 4,5-DIPHENYLIMIDAZOLES
Collibee, William L.,Anselme, Jean-Pierre
, p. 1595 - 1596 (2007/10/02)
Benzil monodisubstituted hydrazones (2) have been shown to undergo cyclodehydration to the corresponding imidazoles (10) and not to pyrazoles as previously reported.
1,3-Dipolar Cycloadditions, 91. The Chemistry of N-Methyl-C-phenylnitrilimine
Fliege, Werner,Grashey, Rudolf,Huisgen, Rolf
, p. 1194 - 1214 (2007/10/02)
The treatment of N'--N-methylhydrazinium bromide, accessible by bromination of benzaldehyde-N-methylhydrazone, with triethylamine furnishes the title compound; this method is superior to the thermolysis and photolysis of 2-methyl-5-phe
