90561-18-5

Upstream product

• 1345024-09-0 2-(3,5-dimethoxy-4-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 22794-95-2 1-bromo-2,4-dimethoxy-3-methylbenzene 
• 5673-07-4 2,6-dimethoxytoluene 
• 78025-93-1 3,5-dimethoxy-4-methylaniline 

Downstream Products

• 253604-35-2 2-{3,5-bis[6-(1H-imidazol-1-yl)hexyloxy]-4-methylphenyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 253604-39-6 2-[3,5-bis(methoxymethoxy)-4-methylphenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 253604-40-9 2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1,3-diol 
• 253604-38-5 5-bromo-1,3-bis(methoxymethoxy)-2-methylbenzene 
• 61203-54-1 4-bromo-2,6-dimethoxy-benzoic acid 
• 253604-37-4 5-bromo-2-methylbenzene-1,3-diol 

Relevant academic research and scientific papers

Total Synthesis of Chaetoglobin A via Catalytic, Atroposelective Oxidative Phenol Coupling

The first total synthesis of chaetoglobin A (1), which features a chiral axis between two identical highly oxygenated bicyclic cores, was successfully completed in 12 steps from 2,6-dimethoxytoluene. Vanadium-catalyzed oxidative phenol coupling, as a key