1383129-55-2

Upstream product

• 1383129-32-5 N-(2,2-diethoxyethyl)-4-methoxy-3,5-dimethylaniline 
• 637-44-5 phenylpropyolic acid 
• 55215-54-8 5-iodo-2-methoxy-1,3-dimethylbenzene 
• 645-36-3 2,2-diethoxy-ethanamine 

Downstream Products

• 1383129-78-9 1-(2,2-diethoxyethyl)-3-iodo-7,9-dimethyl-4-phenyl-1-azaspiro[4.5]deca-3,6,9-triene-2,8-dione 
• 1383129-20-1 2-(3-iodo-7,9-dimethyl-2,8-dioxo-4-phenyl-1-azaspiro[4.5]deca-3,6,9-trien-1-yl)acetaldehyde 
• 1383129-22-3 (6aS,7S,10aR)-2-iodo-7,9-dimethyl-1-phenyl-6a,7-dihydropyrrolo[2,1-i]indole-3,6,8(5H)-trione 

Relevant academic research and scientific papers

Desymmetrization of cyclohexadienones viad-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction

Enantioselective desymmetrization of cyclohexadienones via a d-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction was realized. With 10 mol% of camphor-derived triazolium salt E and 10 mol% of DIEA, various substituted cyclohexadienones proceeded through an intramolecular Stetter reaction, affording tricyclic products in moderate to good yields and excellent ee.