1034980-93-2Relevant academic research and scientific papers
Catalytic Michael reactions of ketoesters with a camphor-derived acrylate equivalent: Stereoselective access to all-carbon quaternary centers
Palomo, Claudio,Oiarbide, Mikel,Garcia, Jesus M.,Banuelos, Patricia,Odriozola, Jose M.,Razkin, Jesus,Linden, Anthony
, p. 2637 - 2640 (2008)
(Chemical Equation Presented) A camphor-based α′-hydroxy enone reagent acts as a chiral acrylate equivalent in copper-catalyzed Michael reactions of β-keto esters and affords products that possess all-carbon quaternary stereocenters of high enantiomeric purity.
