124712-01-2Relevant academic research and scientific papers
Lithium hydroxide catalyzed Michael addition - An easy handling and non-toxic protocol
Sukanya, Kumari,Deka, Dibakar Chandra
experimental part, p. 872 - 875 (2011/08/09)
Michael addition of dimethyl malonate to α,β-unsaturated ketones are reported in the presence of lithium hydroxide as an efficient catalyst of low toxicity, Moderate to high yield at room temperature is an added advantage of the reaction.
Enantioselective Chromatography of Chiral Chalcon-Tricarbonylchromium Complexes and Their Use in Stereoselctive Michael Addition
Gajda, Vladimir,Toma, Stefan,Widhalm, Michael
, p. 147 - 156 (2007/10/02)
The enantiomeres of the title compounds 1 - 8 could be separated by enantioselective chromatography on microcrystalline triacetylcellulose in ethanol.A high stereoselctivity of the Michael addition of dimethylmalonate was ovbserved only for the ortho-subs
