118049-72-2Relevant academic research and scientific papers
Base initiated aromatization/CO bond formation: A new entry to O-pyrazole polyfluoroarylated ethers
Tang, Xiangyang,Chang, Jing,Liu, Cuibo,Zhang, Bin
, p. 6534 - 6537 (2015/01/08)
A base initiated intermolecular SNAr reaction of pyrazolones with polyfluoroarenes was developed. The process involved the isomerization aromatization of pyrazolone followed by the CO bond formation via the selective CF bond cleavage. With this strategy, a wide range of O-pyrazole polyfluoroarylated ethers bearing diverse functional groups were synthesized in mild to good yields. Additionally, our method was also applied to the isoxazol substrates.
A convenient microwave-assisted propylphosphonic anhydride (T3P mediated one-pot pyrazolone synthesis
Desroses, Matthieu,Jacques-Cordonnier, Marie-Caroline,Llona-Minguez, Sabin,Jacques, Sylvain,Koolmeister, Tobias,Helleday, Thomas,Scobie, Martin
supporting information, p. 5879 - 5885 (2013/09/23)
This paper describes a facile, efficient, and clean synthesis of various pyrazolones by employing T3P as a catalyst and performing the reaction under microwave irradiation. This two-step, one-pot reaction proceeded readily and tolerated a variety of functional groups. A wide range of pyrazolone derivatives were obtained in good to excellent yields. A one-pot, two-step procedure for the synthesis of pyrazolones is presented. This method, which uses T3P and microwave irradiation, is particularly easy to carry out and offers a notable alternative to the strongly acidic conditions that are generally employed with other synthetic approaches. Copyright
