1287693-75-7

Upstream product

• 933-67-5 7-methyl-1H-indole 
• 68-12-2 N,N-dimethyl-formamide 
• 100-39-0 benzyl bromide 

Downstream Products

• 1529806-88-9 9-benzyl-4',8-dimethyl-1',2-ditosyl-1,1',2,3,5',9-hexahydro-spiro[pyrido[3,4-b]indole-4,2'-pyrrole] 
• 1584220-36-9 C₂₄H₂₄N₂O₂S 
• 1529806-69-6 N-((1-benzyl-7-methyl-1H-indol-2-yl)methyl)-4-methyl-N-(3-(2-methyl-1-tosylaziridin-2-yl)-prop-2-ynyl)benzenesulfonamide 
• 1584220-32-5 C₂₄H₂₂N₂O₂S 
• 1287693-66-6 1-benzyl-7-methyl-2-vinyl-1H-indole 
• 1169949-15-8 (3S,4R)-9-benzyl-4-ethyl-8-methyl-2,3,4,9-tetrahydro-1H-carbazole-3-carbaldehyde 

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.