1529806-65-2

Upstream product

• 81787-94-2 1-benzylindole-2-carbaldehyde 
• 3377-71-7 N-benzylindole 
• 120-72-9 indole 
• 1584209-01-7 2-(3-(tert-butyldimethylsilyloxy)prop-1-yn-1-yl)-2-methyl-1-tosylaziridine 
• 1584206-86-9 tert-butyldimethyl(4-methylpent-4-en-2-ynyloxy)silane 
• 10605-68-2 4-methyl-4-penten-2-yn-1-ol 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 78-80-8 2-methylbut-1-en-3-yne 
• 1262779-17-8 N-((1-benzylindol-2-yl)methyl)-4-methylbenzenesulfonamide 
• 1584210-03-6 3-(2-methyl-1-tosylaziridin-2-yl)prop-2-yn-1-ol 
• 70-55-3 toluene-4-sulfonamide 
• 100-39-0 benzyl bromide 

Downstream Products

• 1529806-84-5 9-benzyl-4'-methyl-1',2-ditosyl-1,1',2,3,5',9-hexahydro-spiro[pyrido[3,4-b]indole-4,2'-pyrrole] 

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.