163259-70-9

Upstream product

• 100-39-0 benzyl bromide 
• 790715-30-9 (R)-1-((R)-4-Ethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethanol 
• 163259-65-2 (R)-(R)-2-Oxiranyl-but-3-ene-1,2-diol 
• 163259-77-6 (R)-2,2-Dimethyl-4-(R)-oxiranyl-4-vinyl-[1,3]dioxolane 

Relevant academic research and scientific papers

Katsuki-Sharpless Asymmetric Epoxidation of Alkenylethylene Glycols: the Origin of Inverted Stereoselection

The Katsuki-Sharpless asymmetric epoxidation of linear and cyclic alkenylethylene glycols has led to a conclusion that the origin of the inverted stereoselection is due to the simultaneous coordination between both hydroxy groups of the glycol substrates and both titanium atoms in the Ti2(tartrate)2 complex.