469898-52-0

Upstream product

• 469898-42-8 1-(2-allyl-3-benzyloxy-4-methoxy-phenyl)-ethanone 
• 469898-65-5 3-benzyloxy-4-methoxy-1-(1'-hydroxyethyl)-2-(prop-2'-enyl)benzene 
• 469898-57-5 1-acetyl-3-benzyloxy-4-methoxy-2-prop-1'-enylbenzene 
• 18075-42-8 3-benzyloxy-4-methoxy-2-(prop-2'-enyl)benzaldehyde 
• 18075-41-7 2-allyl-3-hydroxy-4-methoxybenzaldehyde 
• 469898-45-1 (R)-3-benzyloxy-4-methoxy-1-(1'-hydroxyethyl)-2-(prop-1''-enyl)benzene 
• 100-39-0 benzyl bromide 

Relevant academic research and scientific papers

Towards the synthesis of chiral isochromanquinones. The use of Corey-Bakshi-Shibata reductions

(1R,3R,4S)-3,4-Dihydro-4-hydroxy-6-methoxy-1,3-dimethylisochroman-5,8-dione has been synthesized in 65% ee from (1R,3R,4S)-5-benzyloxy-3,4-dihydro-4-hydroxy-6-methoxy-1,3-dimethylisochroman by catalytic hydrogenolysis followed by Fremy's salt oxidation of