1456710-51-2

Upstream product

• 1456710-29-4 5-(3-hydroxy-3-methylbut-1-ynyl)-6-(methylamino)-2H-chromen-2-one 
• 106-49-0 p-toluidine 
• 95-51-2 o-chloroaniline 
• 95-79-4 5-chloro-2-methyl-benzenamine 
• 87-60-5 3-chloro-2-methylbenzenamine 
• 583-68-6 2-bromo-p-toluidine 
• 99-09-2 3-nitro-aniline 
• 95-53-4 o-toluidine 
• 162131-02-4 6-(methylamino)-2H-chromen-2-one 
• 1023659-38-2 C₁₀H₈BrNO₂ 

Relevant academic research and scientific papers

Regioselective synthesis of pyrano[3,2-f]quinoline and phenanthroline derivatives using molecular iodine

A series of polysubstituted pyrano[3,2-f]quinoline and phenanthroline derivatives have been synthesized by molecular iodine-catalyzed tandem reaction of various propargylic alcohols with or without substituted amines in excellent yields. Moreover, the cyclized side products are also pyrano[3,2-f]quinoline and phenanthroline derivatives.