120078-16-2

Upstream product

• 39507-96-5 3,5-dimethoxy-α,α-dimethyl benzyl alcohol 
• 5396-64-5 methyl (E)-3-(3,4-dimethoxyphenyl)acrylate 
• 120078-19-5 4-(3,5-Dimethoxy-phenyl)-3-(3,4-dimethoxy-phenyl)-4-methyl-pentanoic acid methyl ester 
• 120078-05-9 2-(3,5-dimethoxyphenyl)-2-bromopropane 
• 2150-37-0 methyl 3,5-dimethoxybenzoate 

Downstream Products

• 120078-42-4 3-(3,4-dihydroxyphenyl)-2,6,8-trihydroxy-4,4-dimethyl-1(4H)-naphthalenone 
• 120078-34-4 3-(3,4-dimethoxyphenyl)-2-hydroxy-6,8-dimethoxy-4,4-dimethyl-1(4H)-naphthalenone 

Relevant academic research and scientific papers

Aryl substituted naphthalene derivatives

Certain aryl substituted naphthalene, benzoxepine, benzazepine and henzocycloheptene derivatives are disclosed. The compounds are useful in treating hyperproliferative skin disease, allergic reactions and inflammation.

SYNTHESIS OF A CARBOCYCLIC ANALOG OF QUERCETIN VIA A BARBIER REACTION

A six-step synthetic route to the carbocyclic flavonoid 2 is described.The key step involves a 1,4-addition of a tertiary bromide to a α,β-unsaturated ester by the Barbier reaction.