1291079-99-6

Upstream product

• 623-03-0 4-Cyanochlorobenzene 
• 932-88-7 1-iodo-2-phenylethyne 
• 58109-40-3 diphenyliodonium hexafluorophosphate 
• 2835-77-0 (2-aminophenyl)(phenyl)methanone 
• 1859-71-8 2-(tosylamino)benzophenone 
• 1238251-92-7 N-(2-(3-(4-chlorophenyl)-1-hydroxy-1-phenylprop-2-ynyl)phenyl)-4-methylbenzenesulfonamide 

Relevant academic research and scientific papers

Synthesis of 3-Iodoquinolines by Copper-Catalyzed Tandem Annulation from Diaryliodoniums, Nitriles, and 1-Iodoalkynes

A novel method for the synthesis of 3-iodoquinolines was developed by copper-catalyzed tandem annulation from diaryliodoniums, nitriles, and 1-iodoalkynes. It is a method that is characterized by the most convenient operation and wide molecular diversity. (Figure presented.) .

Electrophile-driven regioselective synthesis of functionalized quinolines

Highly substituted 3-iodoquinolines bearing different alkyl and aryl moieties can be synthesized in moderate to excellent yields (up to 99%) by 6-endo-dig iodocyclization of 2-tosylaminophenylprop-1-yn-3-ols with molecular iodine (I2) under mil