249763-07-3

Upstream product

• 249762-98-9 bis(1H-2-indolyl)methane 
• 102147-52-4 N-benzyloxymethyl-3,4-dibromomaleimide 
• 200706-56-5 bisindol-2-ylmethan-1-one 
• 80360-23-2 1-(phenylsulfonyl)-1H-indole-2-carbaldehyde 
• 249762-39-8 bis(1-phenylsulfonyl-1H-2-indolyl)methanone 
• 249762-27-4 bis(1-benzenesulfonyl-1H-indol-2-yl)methanol 
• 249762-94-5 bis(1-benzenesulfonyl-1H-indol-2-yl)methane 
• 40899-71-6 1-benzenesulfonylindole 

Downstream Products

• 249763-10-8 2-benzyloxymethyl-8-(2-(N,N-dimethylamino)ethyl)-1,2,3,8,9,10-hexahydroindolo[3',2':5,6]pyrrolo[3',4':3,4]cyclohepta[b]indole-1,3-dione 

Relevant academic research and scientific papers

Homoarcyriaflavin: Synthesis of Ring-Expanded Arcyriaflavin Analogues

The construction of the ring-expanded carbazole system, forming arcyriaflavin homologues, is efficiently accomplished by the reaction of 2,2′-bridged bis-indoles with 3,4-dibromo-2,5-dihydro-1H-2,5-pyrroledione derivatives under Grignard conditions. A ring size of up to nine members in the central ring is achievable. Substitutions either at the indole system or at the imide-N are also possible. The conformation of homoarcyriaflavins as a cross-link between the rigid arcyriaflavins and the flexible arcyriarubins was investigated by NMR, X-ray, and semiempiric quantum chemical calculation methods.