570402-49-2

Upstream product

• 96-32-2 bromoacetic acid methyl ester 
• 55-81-2 4-Methoxyphenethylamine 

Downstream Products

• 570402-53-8 1-[2-(4-methoxy-phenyl)-ethyl]-3,4-bis-trifluoromethanesulfonyloxy-1H-pyrrole-2,5-dicarboxylic acid dimethyl ester 
• 570402-59-4 3,4-bis(4-methoxyphenyl)-1-[2-(4-methoxyphenyl)ethyl]pyrrole-2,5-dicarboxylic acid dimethyl ester 
• 220231-03-8 dimethyl 3,4-bis(3,4,5-trimethoxyphenyl)-1-<2-(4-methoxyphenyl)ethyl>pyrrole-2,5-dicarboxylate 
• 570402-51-6 3,4-dihydroxy-1-[2-(4-methoxy-phenyl)-ethyl]-1H-pyrrole-2,5-dicarboxylic acid dimethyl ester 

Relevant academic research and scientific papers

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.