293315-44-3Relevant academic research and scientific papers
Palladium-catalyzed dehalogenation of 5-halopyrazoles
Chen, Chun-Yen,Huang, Yu-Ying,Su, Wei-Nien,Kaneko, Kimiyoshi,Kimura, Masayuki,Takayama, Hiroyuki,Wong, Fung Fuh
experimental part, p. 183 - 189 (2012/05/05)
A new and efficient method for the dehalogenation of 5-halopyrazoles was developed by using the catalytic amount of palladium (II) chloride and triphenylphosphine as a ligand at reflux under constant flow of hydrogen gas. The reaction gave the correspondi
Cross-coupling of 1-aryl-5-bromopyrazoles: Regioselective synthesis of 3,5-disubstituted 1-arylpyrazoles
Wang, Xiao-Jun,Tan, Jonathan,Grozinger, Karl
, p. 4713 - 4716 (2007/10/03)
The cross-coupling of 1-aryl-5-bromopyrazoles 4 with alkynes, vinyltins and arylboronic acids promoted by Pd(PPh3)4 afforded unsymmetrical 3,5- disubstituted 1-arylpyrazoles 5-8 in excellent yields, 1-Aryl-5- bromopyrazoles 4 were prepared from their corresponding 1-arylpyrazolones 3 with PBr3 in refluxing acetonitrile. (C) 2000 Elsevier Science Ltd.
