THE STEREOSELECTIVE MICHAEL REACTION BETWEEN SILYL ENOL ETHERS AND α,β-UNSATURATED KETONES BY THE USE OF TRITYL PERCHLORATE AS A CATALYST
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.
Mukaiyama, Teruaki,Tamura, Masanori,Kobayashi, Shu
p. 1017 - 1020
(2007/10/02)
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