720712-36-7

Upstream product

• 828933-87-5 2-hydroxy-5-methoxy-4-(2-trimethylsilanyl-ethoxy)-benzaldehyde 
• 2916-68-9 2-(Trimethylsilyl)ethanol 
• 51061-83-7 2,4-dihydroxy-5-methoxybenzaldehyde 
• 720712-34-5 {2-[(2S,4R)-6-Methoxy-4-phenyl-2-((1R,2S)-2-phenyl-cyclohexyloxy)-chroman-7-yloxy]-ethyl}-trimethyl-silane 

Downstream Products

• 828933-81-9 2-((R)-3-Hydroxy-1-phenyl-propyl)-4-methoxy-5-(2-trimethylsilanyl-ethoxy)-phenol 
• 828933-83-1 {2-[2,5-Dimethoxy-4-((R)-1-phenyl-allyl)-phenoxy]-ethyl}-trimethyl-silane 

Relevant academic research and scientific papers

Diastereoselective [4+2] reactions of o-quinone methides with a chiral enol ether: Asymmetric synthesis of (+)-R-mimosifoliol

The first examples of enantioselective [4+2] cycloadditions of o-quinone methides (o-QMs) are reported. Their cycloaddition with trans-2-phenyl-1- cyclohexanol derived vinyl ether produces chiral benzopyrans. This procedure offers access to chiral aliphat