1206199-53-2

Upstream product

• 1206199-52-1 dimethyl 1-[2-(4-isopropoxyphenyl)ethyl]-3,4-bis(trifluoromethanesulfonyloxy)pyrrole-2,5-dicarboxylate 
• 153624-46-5 4-(isopropoxy)phenylboronic acid 

Downstream Products

• 1206199-66-7 dimethyl 3-(4-isopropoxyphenyl)-1-[2-(4-isopropoxyphenyl)ethyl]-4-[7-methoxymethoxy-1-(2-trimethylsilanylethoxymethyl)-indol-3-yl]-pyrrole-2,5-dicarboxylate 
• 1206199-67-8 dimethyl 4-[1-benzyloxymethyl-7-methoxymethoxyindol-3-yl]-3-(4-isopropoxyphenyl)-1-[2-(4-isopropoxyphenyl)ethyl]pyrrole-2,5-dicarboxylate 
• 1206199-68-9 dimethyl 4-[1-tert-butoxycarbonyl-7-diphenylmethoxyindol-3-yl]-3-(4-isopropoxyphenyl)-1-[2-(4-isopropoxyphenyl)ethyl]pyrrole-2,5-dicarboxylate 

Relevant academic research and scientific papers

Synthetic approach to telomerase inhibitor dictyodendrin B: Synthesis of the pyrrolo[2,3-c]carbazole core

The core structure of the telomerase inhibitor, dictyodendrin B, was synthesized by using the palladium-catalyzed cross-coupling reaction of 3-aryl-1-(2-arylethyl)-4-hydroxy-2,5-bismethoxycarbonylpyrrole triflate with 7-alkoxyindole-3-boronate as the key step.