1164124-38-2Relevant academic research and scientific papers
Novel bifunctional sulfonamides catalyze an enantioselective conjugate addition
McGarraugh, Patrick G.,Brenner, Stacey E.
, p. 449 - 455 (2009)
A new bifunctional organocatalyst with a novel structural and functional motif has been developed. This bifunctional sulfonamide organocatalyst was used in the conjugate addition of 1,3-dicarbonyl compounds (13) to β-nitrostyrenes (12). Yields up to 91% a
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.
