125610-66-4Relevant academic research and scientific papers
Iodine-mediated synthesis of 3 H -indoles via intramolecular cyclization of enamines
He, Zhiheng,Li, Huanrong,Li, Zhiping
supporting information; experimental part, p. 4636 - 4639 (2010/09/15)
(Figure presented) The synthesis of 3H-indoles was achieved via the iodine-mediated intramolecular cyclization of enamines. A wide variety of 3H-indole derivatives bearing multifunctional groups were obtained in good to high yields under transition metal-free reaction conditions.
2-Aryl-4-quinolones and Fused Quinolines from β-Chloroarylidenemalonates and Related Chloro Esters
Hormi, Osmo E.,Peltonen, Carita,Heikkilae, Laila
, p. 2513 - 2515 (2007/10/02)
The β-chloroarylidenemalonates I were transformed to the anilinoarylidenemalonates II in 50-70 percent yield.Thermolysis of th β-anilinofurfurylidenemalonate IIc at 250 deg C gave 3-(ethoxycarbonyl)-2-(2-furyl)-4-quinolone III in 85percent yield.Treatment
