1529806-99-2

Upstream product

• 27421-51-8 1-methyl-1H-indole-2-carboxaldehyde 
• 603-76-9 1-methylindole 
• 120-72-9 indole 
• 1529806-79-8 4-methyl-N-(3-(2-methyl-1-tosylaziridin-2-yl)prop-2-ynyl)-N-((1-methyl-1H-indol-2-yl)-methyl)benzenesulfonamide 
• 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 
• 1262779-13-4 4-methyl-N-((1-methyl-1H-indol-2-yl)methyl)benzenesulfonamide 
• 1584210-03-6 3-(2-methyl-1-tosylaziridin-2-yl)prop-2-yn-1-ol 
• 865714-25-6 4-methyl-N-(1-methyl-1H-indol-2-ylmethylene)benzenesulfonamide 
• 70-55-3 toluene-4-sulfonamide 

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.