1265899-59-9

Upstream product

• 151-10-0 1,3-Dimethoxybenzene 
• 16929-70-7 1,3-dimethoxy-2-(1-hydroxy-1-methylethyl)benzene 
• 16700-61-1 1,3-dimethoxy-2-(1-methylethyl)benzene 
• 1305339-26-7 2-(4-isopropyl-3,5-dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Downstream Products

• 1265899-60-2 (R,E)-2-(4-isopropyl-3,5-dimethoxyphenyl)-2-methyl-6-((methyl(phenyl)amino)methylene)-cyclohexanone 
• 1305339-41-6 C₁₉H₂₆O₄ 
• 1265899-61-3 (R)-2-(4-isopropyl-3,5-dimethoxyphenyl)-2-methylcyclohexanone 
• 1265899-62-4 (2R,6S)-6-iodo-2-(2-iodo-4-isopropyl-3,5-dimethoxyphenyl)-2-methylcyclohexanone 
• 1265899-57-7 (R)-2-(4-isopropyl-3,5-dimethoxyphenyl)-2,6,6-trimethylcyclohexanone 
• 1265899-56-6 (4R)-4-(4-isopropyl-3,5-dimethoxyphenyl)-4,8,8-trimethyl-1-oxaspiro[2.5]octane 

Relevant academic research and scientific papers

Total synthesis of agastaquinone, a diterpenoid quinone isolated from Agastache rugosa

Agastaquinone is a tricyclic diterpenoid isolated from Agastache rugose. The first total synthesis of agastaquinone was accomplished based on intramolecular Friedel-Crafts acylation of aryl lactone followed by aromatization leading to the tricyclic phenol

Enantioselective total syntheses of (-)-taiwaniaquinone H and (-)-taiwaniaquinol B by iridium-catalyzed borylation and palladium-catalyzed asymmetric α-arylation

We report a concise, enantioselective total synthesis of (-)-taiwaniaquinone H and the first enantioselective total synthesis of (-)-taiwaniaquinol B by a route that includes asymmetric palladium-catalyzed α-arylation of a ketone with an aryl bromide that