174402-45-0

Upstream product

• 174402-43-8 3-(6-benzyloxy-1H-indol-3-yl)-4-bromo-1-methyl-pyrrole-2,5-dione 
• 153805-86-8 3-Benzyloxy-6-(2-pyrrolidinylvinyl)nitrobenzene 
• 100-44-7 benzyl chloride 
• 24239-67-6 4-(benzyloxy)-1-methyl-2-nitrobenzene 
• 2042-14-0 4-methyl-5-nitrophenol 
• 24424-99-5 di-tert-butyl dicarbonate 
• 15903-94-3 6-benzyloxy-1H-indole 
• 174402-44-9 tert-butyl 6-(benzyloxy)-3-(4-bromo-1-methyl-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-1H-indole-1-carboxylate 

Downstream Products

• 848086-52-2 3-[6-Benzyloxy-1-((2R,4R,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-1H-indol-3-yl]-4-(6-benzyloxy-1H-indol-3-yl)-1-methyl-pyrrole-2,5-dione 
• 848086-51-1 6-Benzyloxy-3-{4-[6-benzyloxy-1-((2R,4R,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-1H-indol-3-yl]-1-methyl-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl}-indole-1-carboxylic acid tert-butyl ester 
• 174402-51-8 2,5-dihydro-3,4-bis-(6-benzyloxy-1H-indol-3-yl)-1-methyl-1H-pyrrole-2,5-dione 

Relevant academic research and scientific papers

Processes for the preparation of indolopyrrolocarbazole derivatives

This invention relates to processes for the preparation of intermediates which are useful in the synthesis of compounds of the general formula or pharmaceutically salts thereof, wherein R1 and R2 each represent an OH group, R1/

Practical synthesis of indolopyrrolocarbazoles

A practical method for the synthesis of an indolo[2,3-a]pyrrolo[3,4- c]carbazole ring system is described. The method involves two key processes: a coupling reaction between indole and substituted methylmaleimide portions using lithium hexamethyldisilazide (LiHMDS) as a base, and the oxidative cyclization of bisindolylmaleimide with palladium (II) chloride. We applied this method to the synthesis of arcyriaflavin B (5), C (6) and D (7).