1466-01-9

Upstream product

• 530-57-4 3,5-dimethoxy-4-hydroxybenzoic acid 
• 106-95-6 allyl bromide 
• 1276653-07-6 allyl-4-(allyloxy)-3,5-dimethoxybenzoate 
• 118-41-2 Eudesmic acid 

Downstream Products

• 66922-68-7 4-allyloxy-3,5-dimethoxyacetophenone 
• 954-85-8 4-Allyloxy-3.5-dimethoxy-benzoylchlorid 
• 6627-88-9 4-allyl-2,6-dimethoxyphenol 
• 1276653-17-8 bis{4-(allyloxy)-3,5-dimethoxyphenyl}methanone 
• 1276653-09-8 tris{4-(allyloxy)-3,5-dimethoxyphenyl}methanone 
• 1276653-10-1 1,1-bis-{4-(allyloxy)-3,5-dimethoxyphenyl}-2-methylbut-3-en-1-ol 
• 1276653-03-2 4,4'-(1-hydroxy-2-methylbut-3-ene-1,1-diyl)bis(2,6-dimethoxyphenol) 
• 1276653-11-2 4,4'-(3-methyltetrahydrofuran-2,2-diyl)bis(2,6-dimethoxyphenol) 
• 34007-64-2 bis(4-hydroxy-3,5-dimethoxyphenyl)methanone 
• 34007-65-3 bis(3,5-dimethoxy-4-acetoxyphenyl)methanone 
• 1276653-12-3 1,1-bis(3,5-dimethoxy-4-acetoxyphenyl)-1-hydroxy-2-methylbut-3-ene 
• 1276653-13-4 2,2-bis(3,5-dimethoxy-4-acetoxyphenyl)-5-hydroxy-3-methyltetrahydrofuran 
• 1276653-14-5 2,2-bis(3,5-dimethoxy-4-acetoxyphenyl)-5-tert-butoxy-3-methyltetrahydrofuran 
• 1276653-15-6 2,2-bis(3,5-dimethoxy-4-acetoxyphenyl)-5-oxo-3-methyltetrahydrofuran 

Relevant academic research and scientific papers

A new convenient synthetic procedure for 4-allyl-2,6-dimethoxyphenol

4-Allyl-2,6-dimethoxyphenol was synthesized from 4-hydroxy-2,6-dimethoxybenzoic acid and allylbromide by condensation under basic condition and by subsequent Claisen rearrangement.

Total synthesis of (±)-sacidumlignan D

The first total synthesis of (±)-sacidumlignan D featuring a Zn-mediated Barbier reaction and reverse Wacker oxidation to form the key γ-lactone, its diastereoselective α-methylation followed by reduction cyclization, was documented.