1264720-07-1Relevant academic research and scientific papers
Synthesis of 2,4-diiodoquinolines via the photochemical cyclization of o-alkynylaryl isocyanides with iodine
Mitamura, Takenori,Ogawa, Akiya
, p. 1163 - 1166 (2011)
Upon photoirradiation of o-alkynylaryl isocyanides in the presence of iodine, the intramolecular cyclization of o-alkynylaryl isocyanides proceeds to afford the corresponding 2,4-diiodoquinolines in good yields. 2,4-Diiodoquinolines can be employed in tra
Thermal aza-bergman cyclization of o-alkynylaryl isocyanides with organic diselenide, ditelluride, and iodine leading to 2,4-difunctionalized quinolines
Mitamura, Takenori,Ogawa, Akiya
supporting information; experimental part, p. 791 - 793 (2011/09/14)
Thermal aza-Bergman cyclization of o-alkynylaryl isocyanides has been achieved in the presence of organic dichalcogenides. The reactions can be induced upon heating at 40 °C to afford the corresponding 2,4-dichalcogenated quinolines. In addition, similar
