105590-62-3

Upstream product

• 35660-91-4 (E)-1-phenyl-2-buten-1-one 
• 66324-10-5 tert-butyldimethyl(1-phenylvinyloxy)silane 
• 100-52-7 benzaldehyde 

Downstream Products

• 109548-66-5 ((2S,3S,4S,6R)-4-Methyl-2,6-diphenyl-tetrahydro-pyran-3-yl)-phenyl-methanone 
• 109548-66-5 ((2S,3R,4R,6S)-4-Methyl-2,6-diphenyl-tetrahydro-pyran-3-yl)-phenyl-methanone 

Relevant academic research and scientific papers

THE TANDEM MICHAEL-ALDOL REACTION CATALYZED BY TRITYL PERCHLORATE

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

TRITYL PERCHLORATE CATALYZED TANDEM MICHAEL-ALDOL REACTION. A FACILE METHOD FOR THE STEREOSELECTIVE SYNTHESES OF γ-ACYL SUBSTITUTED δ-HYDROXY KETONE DERIVATIVES

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