197382-79-9

Upstream product

• 221123-50-8 7-(3-isopropoxy-4-methoxyphenyl)-3-oxoheptanoic acid methyl ester 
• 221123-48-4 3-(3-isopropyloxy-4-methoxyphenyl)propanol-1 
• 221123-49-5 3-(3-isopropyloxy-4-methoxyphenyl)propyl iodide 
• 15017-52-4 4-(bromomethyl)-1-fluoro-2-nitrobenzene 
• 129150-61-4 3-(3-hydroxy-4-methoxyphenyl)-propionic acid methyl ester 
• 221123-51-9 4-fluoro-3-nitrobenzyl iodide 
• 197382-92-6 2-(4-fluoro-3-nitrobenzyl)-7-(3-isopropoxy-4-methoxyphenyl)-3-oxoheptanoic acid methyl ester 

Downstream Products

• 221123-62-2 1-(4-fluoro-3-nitrophenyl)-7-(3-isopropoxy-4-methoxyphenyl)heptanol-3 
• 1026879-23-1 methanesulfonic acid 1-[2-(4-fluoro-3-nitro-phenyl)-ethyl]-5-(3-isopropoxy-4-methoxy-phenyl)-pentyl ester 
• 221123-63-3 1-(4-fluoro-3-nitrophenyl)-7-(3-isopropoxy-4-methoxyphenyl)-3-iodoheptane 
• 221123-64-4 1-(4-fluoro-3-nitrophenyl)-7-(3-isopropoxy-4-methoxyphenyl)heptane 
• 221123-65-5 5-[7-(4-fluoro-3-nitrophenyl)heptyl]-2-methoxyphenol 

Relevant academic research and scientific papers

A unified strategy toward the synthesis of acerogenin-type macrocycles: Total syntheses of acerogenins A, B, C, and L and aceroside IV

A general strategy for the synthesis of acerogenin-type diarylheptanoids containing an endocyclic biaryl ether bond has been developed, and convergent total syntheses of acerogenin A, B, C, and L and aceroside IV have been accomplished. Cycloetherificatio