174402-47-2

Upstream product

• 15903-94-3 6-benzyloxy-1H-indole 
• 174402-50-7 3-[6-Benzyloxy-1-((2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-1H-indol-3-yl]-4-bromo-1-methyl-pyrrole-2,5-dione 
• 174402-43-8 3-(6-benzyloxy-1H-indol-3-yl)-4-bromo-1-methyl-pyrrole-2,5-dione 
• 6564-72-3 2,3,4,6-tetra-O-benzyl-D-glucopyranose 

Downstream Products

• 174402-48-3 12,13-dihydro-2,10-dibenzyloxy-13-(β-D-2,3,4,6-tetra-O-benzylglucopyranosyl)-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-6-methyl-5,7(6H)-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/

Synthesis of dissymmetric indolocarbazole glycosides using the Mitsunobu reaction at the glycosylation step

A novel method for the synthesis of N-glycosylated dissymmetric indolo[2,3-a]pyrrolo-[3,4-c]carbazole derivatives was developed by applying the Mitsunobu reaction to the N-glycosylation reaction of substituted indole substrates.