107995-06-2Relevant academic research and scientific papers
THE STEREOSELECTIVE MICHAEL REACTION BETWEEN SILYL ENOL ETHERS AND α,β-UNSATURATED KETONES BY THE USE OF TRITYL PERCHLORATE AS A CATALYST
Mukaiyama, Teruaki,Tamura, Masanori,Kobayashi, Shu
, p. 1017 - 1020 (2007/10/02)
The Michael adducts are obtained with good to excellent ul selectivity by treating silyl enol ethers with α,β-unsaturated ketones in the presence of a catalytic amount of trityl perchlorate.
