1390642-46-2

Upstream product

• 1390642-45-1 (E)-methyl 3-(4-(benzyloxy)-2-hydroxy-3-methoxyphenyl)acrylate 
• 1390642-33-7 (E)-methyl 3-(4-(benzyloxy)-2-isopropoxy-3-methoxyphenyl)acrylate 
• 65535-52-6 7-benzyloxy-8-methoxycoumarin 

Downstream Products

• 1390642-47-3 1-(3-bromo-4-isopropoxyphenyl)-7-(4-hydroxy-2-isopropoxy-3-methoxyphenyl)heptan-3-one 
• 1390642-48-4 1-(3-bromo-4-methoxyphenyl)-7-(4-hydroxy-2-isopropoxy-3-methoxyphenyl)heptan-3-one 
• 1390642-32-6 (E)-3-(4-(benzyloxy)-2-isopropoxy-3-methoxyphenyl)acrylaldehyde 
• 1390642-35-9 (4E,6E)-7-(4-(benzyloxy)-2-isopropoxy-3-methoxyphenyl)-1-(3-bromo-4-isopropoxyphenyl)hepta-4,6-dien-3-one 
• 1390642-38-2 (4E,6E)-7-(4-(benzyloxy)-2-isopropoxy-3-methoxyphenyl)-1-(3-bromo-4-methoxyphenyl)hepta-4,6-dien-3-one 

Relevant academic research and scientific papers

Chirality in diarylether heptanoids: Synthesis of myricatomentogenin, jugcathanin, and congeners

The syntheses of myricatomentogenin, jugcathanin, galeon, pterocarine, and acerogenin L are reported. Synthetic material was used to measure their optical activities and free energy of activation for racemization. The natural enantiomers of myricatomentog