127229-92-9

Upstream product

• 100-63-0 phenylhydrazine 
• 618-40-6 1-Methyl-1-phenylhydrazine 
• 127229-86-1 (6α,6aα,12α,12aα)-5,6,6a,11,12,12a-Hexahydro-5,11-dimethylpentaleno<2,1-b:5,4-b'>diindole-6,12-diol 
• 127229-85-0 cis-5,6,6a,11,12,12a-Hexahydro-5,11-dimethylpentaleno<2,1-b:5,4-b'>diindole 
• 127229-84-9 cis-5,6,6a,11,12,12a-Hexahydro-5,11-dihydropentaleno<2,1-b:5,4-b'>diindole 
• 51716-63-3 cis-bicyclo[3. 3. 0]octane-3,7-dione 
• 127229-87-2 cis-5,6a,11,12a-Tetrahydro-5,11-dimethylpentaleno<2,1-b:5,4-b'>diindole-6,12-dione 
• 591-51-5 phenyllithium 

Downstream Products

• 127229-94-1 <3-(1,4-Dihydro-4-methyl-2-phenylcyclopentindol-1-yl)-1-methyl-1H-indol-2-yl>phenylmethanone 
• 127229-95-2 <1-Methyl-3-(1,2,3,4-tetrahydro-4-methyl-3-phenyl-1-(phenylseleno)cyclopentindol-2-yl)-1H-indol-2-yl>phenylmethanone 
• 127229-96-3 4-Methyl-1-[1-(1-methyl-1H-indol-2-yl)-1-phenyl-meth-(E)-ylidene]-3-phenyl-1,4-dihydro-cyclopenta[b]indole 
• 127229-93-0 C₃₄H₂₆N₂O 
• 127229-93-0 C₃₄H₂₆N₂O 

Relevant academic research and scientific papers

Synthetic Approach to Pentalenodiindoles

A combination of the Weiss reaction and the Fischer indole cyclization was employed to prepare the hexahydro-5,11-dihydropentalenodiindoles 8 and 10.These diindole perhydropentalenes were converted into a variety of 6,12-disubstituted deriva