75510-58-6

Upstream product

• 93092-14-9 1-bromo-5-hydroxy-2,3-dimethoxybenzene 
• 6948-30-7 5-bromoveratralaldehyde 
• 2973-76-4 5-bromo-4-hydroxy-3-methoxybenzaldehyde 
• 121-33-5 vanillin 
• 23030-39-9 1-bromo-2,3,5-trimethoxybenzene 

Downstream Products

• 75510-59-7 1-(2,3,5-trimethoxy-phenyl)-ethanone 
• 5556-84-3 2,3,5-trimethoxy-benzaldehyde 
• 153335-58-1 N-(2-Hydroxy-1,1-dimethyl-ethyl)-2,3,5-trimethoxy-benzamide 
• 119098-79-2 2,3,5-Trimethoxy-benzoyl chloride 
• 119098-80-5 4,5-dihydro-2-(2,3,5-trimethoxyphenyl)-4,4-dimethyloxazole 
• 311313-46-9 2,3,5-trimethoxybenzamide 
• 36873-96-8 2,3,5-trimethoxybenzoic acid 

Relevant academic research and scientific papers

Attempt to synthesize 2,3,5,4′-tetrahydroxystilbene derived from 2,3,5,4′-tetrahydroxystilbene-2-O-β-glucoside (THSG)

An attempt to synthesize aglycone 1 derived from 2,3,5,4′-tetrahydroxystilbene-2-O-β-glucoside (THSG) via the Wittig reaction and Mizoroki-Heck reaction is described. In the Wittig protocol, 2,3,5,4′-tetramethoxystilbene 2 was obtained. Additionally, a palladium-catalyzed Mizoroki-Heck reaction strategy yielded 2-aryl-2,3-dihydrobenzofuran 13 instead of derivative 12 in good yield.

THE SYNTHESIS OF DESERTORIN C, A BICOUMARIN FROM THE FUNGUS EMERICELLA DESERTORUM

The structure of desertorin C, a metabolite of the mould Emericella desertorum, is confirmed as 4,4',7,7'-tetramethoxy-5,5'-dimethyl-6,8'-bicoumarin (6), by its synthesis in racemic form.The key step involved the construction of the unsymmetrical biphenyl