6132-87-2

Upstream product

• 615-43-0 2-iodophenylamine 
• 1078-19-9 6-methoxy-3,4-dihydro-1(2H)-naphthalenone 

Downstream Products

• 848771-89-1 4,13-dihydro-4,4-diphenyl-1-benzopyran[6,5-a]carbazole 
• 6132-92-9 3-hydroxybenzo[a]carbazole 
• 1210470-17-9 C₃₄H₂₂ClN 
• 1210468-66-8 C₅₈H₄₀N₂ 
• 1210468-90-8 C₅₂H₃₆N₂ 
• 1210469-95-6 C₂₃H₁₇NO 
• 1210469-97-8 C₂₂H₁₅NO 
• 1210469-99-0 C₂₉H₂₁NO 
• 1210470-01-1 C₂₈H₁₉NO 
• 1210470-04-4 C₂₈H₁₉N 
• 1210470-05-5 C₂₈H₁₈ClN 
• 1210470-10-2 C₂₈H₁₈BrN 

Relevant academic research and scientific papers

One pot synthesis of substituted dihydroindeno[1,2-b]indoles and dihydrobenzo[a]carbazoles by photostimulated reactions of o-iodoaniline with carbanions by the SRN1 mechanism

The photostimulated reaction of enolate anions of cyclic aromatic ketones such as substituted indan-1-ones and 3,4-dihydro-2H-naphthalen-1-one with o-iodoaniline in DMSO affords 1-, 2-, 3-, and 4-methoxy-5,10-dihydroindeno[1,2- b]indoles (34-40%), 1,2-, 1,4-, and 2,3-dimethoxy-5,10-dihydroindeno[1,2-b]- indoles (31-43%), and 1-, 2-, and 3-methoxy-5,11-dihydro-6H-benzo[a]carbazoles (42-61%) by the SRN1 mechanism in one pot reactions.