1584209-01-7

Upstream product

• 10605-68-2 4-methyl-4-penten-2-yn-1-ol 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 1584206-86-9 tert-butyldimethyl(4-methylpent-4-en-2-ynyloxy)silane 
• 78-80-8 2-methylbut-1-en-3-yne 
• 70-55-3 toluene-4-sulfonamide 

Downstream Products

• 1529806-85-6 9-benzyl-4',5-dimethyl-1',2-ditosyl-1,1',2,3,5',9-hexahydro-spiro[pyrido[3,4-b]indole-4,2'-pyrrole] 
• 1529806-86-7 9-benzyl-4',6-dimethyl-1',2-ditosyl-1,1',2,3,5',9-hexahydro-spiro[pyrido[3,4-b]indole-4,2'-pyrrole] 
• 1529806-87-8 9-benzyl-4',7-dimethyl-1',2-ditosyl-1,1',2,3,5',9-hexahydro-spiro[pyrido[3,4-b]indole-4,2'-pyrrole] 
• 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] 
• 1529806-89-0 9-benzyl-5-methoxy-4'-methyl-1',2-ditosyl-1,1',2,3,5',9-hexahydrospiro[pyrido[3,4-b]indole-4,2'-pyrrole] 
• 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] 
• 1529806-92-5 9-benzyl-7-chloro-4'-methyl-1',2-ditosyl-1,1',2,3,5',9-hexa-hydrospiro[pyrido[3,4-b]indole-4,2'-pyrrole] 
• 1529806-95-8 7-benzyl-4'-methyl-1',9-ditosyl-1',5',7,8,9,10-hexahydro-spiro[benzo[e]pyrido[3,4-b]indole-11,2'-pyrrole] 
• 1529806-97-0 5-benzyl-4'-methyl-1',7-ditosyl-1',5,5',6,7,8-hexahydro-spiro[[1,3]dioxolo[4,5-f]pyrido[3,4-b]indole-9,2'-pyrrole] 
• 1529806-99-2 4',9-dimethyl-1',2-ditosyl-1,1',2,3,5',9-hexahydrospiro-[pyrido[3,4-b]indole-4,2'-pyrrole] 
• 1529807-00-8 9-ethyl-4'-methyl-1',2-ditosyl-1,1',2,3,5',9-hexahydro-spiro[pyrido[3,4-b]indole-4,2'-pyrrole] 
• 1529807-01-9 9-allyl-4'-methyl-1',2-ditosyl-1,1',2,3,5',9-hexahydro-spiro[pyrido[3,4-b]indole-4,2'-pyrrole] 
• 1584210-03-6 3-(2-methyl-1-tosylaziridin-2-yl)prop-2-yn-1-ol 
• 1529806-65-2 N-((1-benzyl-1H-indol-2-yl)methyl)-4-methyl-N-(3-(2-methyl-1-tosylaziridin-2-yl)prop-2-ynyl)benzenesulfonamide 

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.