676546-90-0

Upstream product

• 91-16-7 1,2-dimethoxybenzene 
• 14003-11-3 5-methylfuran-2-carbonyl chloride 
• 677299-77-3 (3,4-dimethoxy-phenyl)-(5-methyl-furan-2-yl)-methanone 
• 676546-91-1 (4,5-dimethoxy-2-nitrophenyl)-(5-methyl-2-furyl)-methanone 

Downstream Products

• 1318849-88-5 (3E)-4-[6,7-dimethoxy-2-(2-nitrophenyl)quinolin-3-yl]but-3-en-2-one 
• 1318849-87-4 (3E)-4-(6,7-dimethoxy-2-phenylquinolin-3-yl)but-3-en-2-one 
• 1318850-01-9 N-{4,5-dimethoxy-2-[(5-methyl-2-furyl)methyl]phenyl}thiophene-2-carboxamide 
• 1318849-98-7 N-{4,5-dimethoxy-2-[(5-methyl-2-furyl)methyl]phenyl}-2-nitrobenzamide 
• 1318849-96-5 N-{4,5-dimethoxy-2-[(5-methyl-2-furyl)methyl]phenyl}acetamide 
• 1318849-97-6 N-{4,5-dimethoxy-2-[(5-methyl-2-furyl)methyl]phenyl}benzamide 
• 924635-50-7 4-methyl-N-{4,5-dimethoxy-2-[(5-methylfuran-2-yl)methyl]phenyl}benzenesulfonamide 

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.

Simple route to 3-(2-indolyl)-1-propanones via a furan recyclization reaction

A simple route to 1-R-3-(2-indolyl)-1-propanones has been elaborated based on recyclization of 2-(2-aminobenzyl)furan derivatives. Being a modification of the Reissert indole synthesis, our approach employs the furan ring as a source of carbonyl function. This approach is general and allows varying of substituents in aromatic ring as well as in 3-position of indole nucleus.