105590-56-5Relevant academic research and scientific papers
TRITYL PERCHLORATE CATALYZED TANDEM MICHAEL-ALDOL REACTION. A FACILE METHOD FOR THE STEREOSELECTIVE SYNTHESES OF γ-ACYL SUBSTITUTED δ-HYDROXY KETONE DERIVATIVES
Kobayashi, Shu,Mukaiyama, Teruaki
, p. 221 - 224 (1986)
In the presence of a catalytic amount of trityl perchlorate, the intermediate adducts, produced in situ by the conjugate addition of silyl enol ethers with α,β-unsaturated ketones, react with aldehydes to give the corresponding γ-acyl substituted δ-hydrox
THE TANDEM MICHAEL-ALDOL REACTION CATALYZED BY TRITYL PERCHLORATE
Mukaiyama, Teruaki,Kobayashi, Shu
, p. 205 - 211 (2007/10/02)
In the presence of a catalytic amount of trityl perchlorate, the tandem reaction of conjugate addition of silyl enol ethers to α,β-unsaturated ketones, and the sequential aldol reaction with aldehydes is carried out smoothly to afford γ-acyl-substituted δ
