61576-08-7

Upstream product

• 594858-52-3 3-(3-bromo-4-isopropoxy-phenyl)propionic acid methyl ester 
• 1390642-40-6 (4E,6E)-7-(4-(benzyloxy)-3-methoxyphenyl)-1-(3-bromo-4-isopropoxyphenyl)hepta-4,6-dien-3-one 
• 1390642-34-8 dimethyl (4-(3-bromo-4-isopropoxyphenyl)-2-oxobutyl)phosphonate 
• 1390642-41-7 (+/-)-isopropyl galeon 
• 1390642-49-5 1-(3-bromo-4-isopropoxyphenyl)-7-(4-hydroxy-3-methoxyphenyl)heptan-3-one 
• 936253-55-3 1-(3-bromo-4-benzyloxyphenyl)-7-(4-hydroxy-3-methoxyphenyl)heptan-3-one 
• 936253-53-1 6-(4-hydroxy-3-methoxyphenyl)hexan-2-one 
• 936253-56-4 4-benzyloxy-17-methoxy-2-oxatricyclo[13.2.2.1^3,7]eicosa-1⁽¹⁸⁾,3⁽²⁰⁾,4,6,15⁽¹⁹⁾,16-hexaen-10-one 
• 77795-21-2 (E)-3-[4-(benzyloxy)-3-methoxyphenyl]acrylaldehyde 

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

First total synthesis of cytotoxic diarylheptanoids, galeon, and pterocarine

The first total synthesis of cytotoxic diphenyl ether-type diarylheptanoids, galeon and pterocarine, was described in which the Ullmann reaction was employed at the final step for the diaryl ether formation of key intermediate, 1-(3-bromo-4-benzyloxypheny

A versatile synthesis of cyclic diphenyl ether-type diarylheptanoids: Acerogenins, (±)-galeon, and (±)-pterocarine

A versatile method for the total synthesis of cyclic diphenyl ether-type diarylheptanoids, acerogenin C, acerogenin L, (±)-galeon, and (±)-pterocarine was described. The Ullmann reaction of suitably substituted linear diphenylheptanoids was employed for t