138690-10-5Relevant academic research and scientific papers
Stereoselective Michael Addition Reactions of Acylated Oxazolidinones to Ethyl 3-Trifluoromethylacrylate
Yamazaki, Takashi,Haga, Jiro,Kitazume, Tomoya
, p. 2175 - 2178 (1991)
Michael addition reactions of acyl oxazolidinones to ethyl 3-trifluoromethylacrylate were found to proceed smoothly with a high degree of diastereo- as well as diastereofacial selectivity at the new carbon-carbon bond.
Stereoselective Synthesis of Trifluoromethylated Compounds with Controlled Adjacent Tertiary Carbons by Michael Addition to (E)-3-(Trifluoromethyl)acrylates
Shinohara, Noriyasu,Haga, Jiro,Yamazaki, Takashi,Kitazume, Tomoya,Nakamura, Shinichiro
, p. 4363 - 4374 (2007/10/02)
Michael addition reaction of various lithium enolates to ethyl (E)-3-(trifluoromethyl)acrylate (E)-1 was found to be one of the most effective routes to construct materials not only with a CF3 group but also readily distinguishable multiple functionalitie
