1339872-52-4

Upstream product

• 57489-92-6 5-tert-butyl-furan-2-carbonyl chloride 
• 91-16-7 1,2-dimethoxybenzene 

Downstream Products

• 1339872-56-8 (2-amino-4,5-dimethoxyphenyl)(5-tert-butyl-2-furyl)methanone 
• 1339872-58-0 C₁₇H₂₃NO₃ 
• 1318849-99-8 N-{2-[(5-tert-butyl-2-furyl)methyl]-4,5-dimethoxyphenyl}benzamide 
• 1339872-43-3 N-{2-[(5-tert-butyl-2-furyl)methyl]-4,5-dimethoxyphenyl}-2-phenylacetamide 
• 1339872-44-4 N-{2-[(5-tert-butyl-2-furyl)methyl]-4,5-dimethoxyphenyl}-2-chloroacetamide 
• 1318849-89-6 (1E)-1-(6,7-dimethoxy-2-phenylquinolin-3-yl)-4,4-dimethylpent-1-en-3-one 
• 1339872-46-6 (1E)-1-(2-benzyl-6,7-dimethoxyquinolin-3-yl)-4,4-dimethylpent-1-en-3-one 
• 1339872-54-6 (5-tert-butyl-2-furyl)(4,5-dimethoxy-2-nitrophenyl)methanone 

Relevant academic research and scientific papers

Furan ring opening - Pyridine ring closure: New route to quinolines under the Bischler-Napieralski reaction conditions

A new approach to highly functionalized quinolines is proposed. This approach is based on the electrophilic recyclization of 2-[2-(acylamino)benzyl] furans under the Bischler-Napieralski reaction conditions. Georg Thieme Verlag Stuttgart. New York.