34889-56-0Relevant academic research and scientific papers
Conversion of carbon dioxide into 2-oxazolidinones and 2(3H)-oxazolones catalyzed by 2,2′,2″-terpyridine
Liu, Huixin,Hua, Ruimao
, p. 1200 - 1204 (2016/02/16)
The catalytic activation of pyridines as organocatalysts in the three-component cycloaddition of CO2, propargyl alcohol and primary amine was investigated, and 2,2′,2″-Terpyridine was found to be the efficient organocatalyst to afford 4-methylene-2-oxazolidinones or 2(3H)-oxazolones in good to high yields. 2,2′,2″-Terpyridine also showed high catalytic activity in the coupling reaction of CO2 with aziridines bearing either electron-donating or electron-withdrawing N-substituents to give substituted 2-oxazolidinones in high yields.
Enantioselective organocatalytic michael addition of nitroalkanes and other nucleophiles to β-trifluoromethylated acrylamides
Wen, Lele,Yin, Liang,Shen, Qilong,Lu, Long
supporting information, p. 502 - 506 (2013/05/22)
An organocatalytic asymmetric Michael addition of nitroalkanes to trifluoromethylated acrylamides in good yields and with good to excellent diastereoselectivities and excellent enantioselectivities is described. The Michael adducts could be readily transf
