570402-59-4

Upstream product

• 5720-07-0 4-methoxyphenylboronic acid 
• 570402-53-8 1-[2-(4-methoxy-phenyl)-ethyl]-3,4-bis-trifluoromethanesulfonyloxy-1H-pyrrole-2,5-dicarboxylic acid dimethyl ester 
• 917479-37-9 3,4-bis(4-methoxyphenyl)-1-[2-(4-methoxyphenyl)ethyl]pyrrole-2,5-dicarboxylic acid 
• 74-88-4 methyl iodide 
• 570402-51-6 3,4-dihydroxy-1-[2-(4-methoxy-phenyl)-ethyl]-1H-pyrrole-2,5-dicarboxylic acid dimethyl ester 
• 570402-49-2 {methoxycarbonylmethyl-[2-(4-methoxy-phenyl)-ethyl]-amino}-acetic acid methyl ester 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 55-81-2 4-Methoxyphenethylamine 
• 28030-16-2 3-(4-methoxyphenyl)-2-oxopropanoic acid 

Downstream Products

• 917479-33-5 {5-(4-methoxybenzoyl)-3,4-bis(4-methoxyphenyl)-1-[2-(4-methoxyphenyl)ethyl]-1H-pyrrol-2-yl}-(4-methoxyphenyl)methanone 

Relevant academic research and scientific papers

Synthesis of polycitrin A and 3,4-bis(4-hydroxyphenyl)pyrrole derivatives related to polycitone A

The oxidative condensation of 3-arylpyruvic acids with arylethylamines to give 3,4-diarylpyrrole-2,5-dicarboxylic acids was used for an efficient synthesis of polycitrin A (4). Investigation of the bromine-mediated degradation of acid 2b to maleimide 3b s

Short and flexible route to 3,4-diarylpyrrole marine alkaloids: Syntheses of permethyl storniamide A, ningalin B, and lamellarin G trimethyl ether

A highly efficient route to 3,4-diarylpyrrole marine alkaloids has been developed using Hinsberg-type pyrrole synthesis and palladium-catalyzed Suzuki cross-coupling of the 3,4-dihydroxypyrrole bis-triflate derivatives as key reactions. Based on this approach, formal syntheses of permethyl storniamide A and ningalin B, and a total synthesis of lamellarin G trimethyl ether have been achieved.