550365-35-0

Upstream product

• 91-52-1 2,4 dimethoxybenzoic acid 
• 126065-87-0 1,2-dimethoxy-4-(prop-1-yn-1-yl)benzene 
• 550365-26-9 methyl 4,6-dimethoxy-2-(perfluoro-1-butanesulfonyloxy)benzoate 
• 550365-27-0 methyl 4,6-dimethoxy-2-[(3,4-dimethoxyphenyl)ethynyl]benzoate 
• 29723-28-2 methyl 2,4,6-trimethoxybenzoate 
• 51116-92-8 methyl 4,6-dimethoxysalicylate 
• 594-27-4 tetramethylstannane 
• 550365-22-5 4-iodo-6,8-dimethoxy-3-(3,4-dimethoxyphenyl)isocoumarin 

Relevant academic research and scientific papers

Ruthenium(II)-catalyzed C-H activation/alkyne annulation by weak coordination with O2 as the sole oxidant

Aerobic oxidative C-H functionalizations of weakly coordinating benzoic acids have been accomplished with versatile ruthenium(II) biscarboxylates under ambient oxygen or air. Mechanistic studies identified the key factors controlling the elementary step o

Synthesis of 3-arylisocoumarins, including thunberginols A and B, unsymmetrical 3,4-disubstituted isocoumarins, and 3-ylidenephthalides via iodolactonization of methyl 2-ynylbenzoates or the corresponding carboxylic acids

3-Aryl-4-iodoisocoumarins, which were readily and efficiently prepared by regioselective iodolactonization of methyl 2-ynylbenzoates or the corresponding carboxylic acids, were used as precursors either to 3-arylisocoumarins, including naturally-occurring