102076-72-2Relevant academic research and scientific papers
Mechanosynthesis of γ-nitro dicarbonyl compounds via CaCl 2-catalyzed Michael addition
Jia, Chunman,Chen, Da,Zhang, Chunyan,Zhang, Qi,Cao, Bennan,Zhao, Zhendong
, p. 7320 - 7324 (2013/08/23)
An efficient strategy for the mechanosynthesis of γ-nitro dicarbonyl esters has been developed. A CaCl2-catalyzed Michael reaction, conducted at room temperature, afforded nitroalkenes from malonates in a short reaction time and in high yields.
