1016169-41-7Relevant academic research and scientific papers
Regioselective, One-Pot, Three-Component Synthesis of 1,3,4- and 1,3,5-Triarylpyrazoles from 1- and 2-Aryl-1-alkenyl Sulfones
Fuse, Shinichiro,Sugiyama, Hirotaka,Kobayashi, Daisuke,Iijima, Yusuke,Matsumura, Keisuke,Tanaka, Hiroshi,Takahashi, Takashi
, p. 4756 - 4764 (2015)
A one-pot, three-component coupling of aldehydes with hydrazines and 1-aryl-1-alkenyl sulfones or 2-aryl-1-alkenyl sulfones for the regioselective synthesis of 1,3,4- and 1,3,5-triarylpyrazoles was developed. In our developed procedure, 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) worked as an effective oxidant, and the addition of an strong acid was not necessary. We synthesized 1,3,4- and 1,3,5-triarylpyrazoles containing acid-labile functionalities in a one-pot reaction in good yields.
Base-mediated reaction of hydrazones and nitroolefins with a reversed regioselectivity: A novel synthesis of 1,3,4-Trisubstituted pyrazoles
Deng, Xiaohu,Mani, Neelakandha S.
supporting information; body text, p. 1307 - 1310 (2009/04/06)
A regioselective synthesis of 1,3,4-tri- or 1,3,4,5-tetrasubstituted pyrazoles by the reaction of hydrazones with nitroolefins is described. Mediated with strong bases such as t-Bu OK, the reaction exhibits a reversed, exclusive 1,3,4-regioselectivity. Su
