1320362-77-3

Upstream product

• 772-38-3 4-tert-Butylphenylacetylene 
• 73568-25-9 2-chloro-3-quinoline carboxaldehyde 
• 67-56-1 methanol 
• 1256285-91-2 2-((4-(tert-butyl)phenyl)ethynyl)quinoline-3-carbaldehyde 

Downstream Products

• 1320362-27-3 C₃₀H₂₉NO₃ 
• 1398566-89-6 3-(4-(tert-butyl)phenyl)-4-((4-butylphenyl)ethynyl)-1-methoxy-1H-pyrano[4,3-b]quinoline 
• 1398566-88-5 3-(4-(tert-butyl)phenyl)-1-methoxy-4-(p-tolylethynyl)-1H-pyrano[4,3-b]quinoline 
• 1398567-09-3 3-(4-(tert-butyl)benzoyl)-1-(4-butylphenyl)pyrrolo[1,2-a]quinoline-4-carbaldehyde 
• 1398567-08-2 3-(4-(tert-butyl)benzoyl)-1-(p-tolyl)pyrrolo[1,2-a]quinoline-4-carbaldehyde 

Relevant academic research and scientific papers

Site-selective electrophilic cyclization and subsequent ring-opening: A synthetic route to pyrrolo[1,2-a]quinolines and indolizines

An efficient strategy for the synthesis of pyrrolo[1,2-a]quinolines and indolizines from pyranoquinolines via site-selective electrophilic cyclization and subsequent opening of pyran ring using silver/iodine under mild reaction conditions is described. Th

Pyrano[4,3-b]quinolines library generation via iodocyclization and palladium-catalyzed coupling reactions

Synthesis of a 80-member library of novel pyrano[4,3-b]quinolines in solution-phase is reported. The key intermediate, 4-iodopyrano[4,3-b]quinolines were synthesized by the electrophilic iodocyclization of corresponding ortho-alkynyl aldehydes in good to