178047-39-7

Upstream product

• 1006-94-6 5-methoxylindole 
• 16382-21-1 1-benzyl-5-methoxyindole 
• 68-12-2 N,N-dimethyl-formamide 
• 100-39-0 benzyl bromide 
• 21778-81-4 5-methoxy-1H-indole-2-carbaldehyde 

Downstream Products

• 1529806-90-3 9-benzyl-6-methoxy-4'-methyl-1',2-ditosyl-1,1',2,3,5',9-hexahydrospiro[pyrido[3,4-b]indole-4,2'-pyrrole] 
• 1529806-71-0 N-((1-benzyl-5-methoxy-1H-indol-2-yl)methyl)-4-methyl-N-(3-(2-methyl-1-tosylaziridin-2-yl)prop-2-ynyl)benzenesulfonamide 
• 1584220-56-3 C₂₄H₂₂N₂O₃S 
• 1169949-31-8 (3R,4R)-9-benzyl-6-methoxy-4-(trimethylsilyl)-2,3,4,9-tetrahydro-1H-carbazole-3-carbaldehyde 
• 1169949-27-2 (3S,4R)-9-benzyl-4-(2,4-dichlorophenyl)-6-methoxy-2,3,4,9-tetrahydro-1H-carbazole-3-carbaldehyde 
• 1169949-00-1 (3S,4R)-9-benzyl-4-ethyl-6-methoxy-2,3,4,9-tetrahydro-1H-carbazole-3-carbaldehyde 
• 1146472-93-6 1-benzyl-5-methoxy-2-vinyl-1H-indole 
• 178047-45-5 (E)-N-benzyl-2-(4-hydroxypentyl)-5-methoxy-3-(2-nitroethenyl)indole 
• 178047-49-9 1-(9-Benzyl-6-methoxy-4-nitromethyl-2,3,4,9-tetrahydro-1H-carbazol-3-yl)-ethanone 
• 178047-47-7 (E)-N-benzyl-5-methoxy-3-(2-nitroethenyl)-2-(4-oxopentyl)indole 
• 178047-43-3 N-benzyl-2-(4-hydroxypentyl)-5-methoxyindole 

Relevant academic research and scientific papers

Gold(I)-catalyzed rearrangement of alkynylaziridine indoles for the synthesis of spiro-tetrahydro-β-carbolines

Functionalized spiro-tetrahydro-β-carbolines were formed by an efficient gold(I)-catalyzed rearrangement reaction of alkynylaziridine indoles. The reaction involved a Friedel-Crafts type intramolecular reaction of alkynylaziridine indoles, following by hydroamination of aminoallene intermediate.

Synthesis of carbazole derivatives - III. Synthesis of new pyrrolidino[3,4-c]carbazoles by intramolecular Michael addition

We have reported on the synthesis of carbazoles by inter- and intramolecular Michael addition. Ellipticine derivatives are related to these compounds, and especially those with 9-methoxy- and 9-hydroxy substituents exhibit appreciable antitumor and antile