Beesu, Mallesh Mehta, Goverdhan Synthesis of Quinolines and Isoquinolines via Site-Selective, Domino Benzannulation of 2- and 3‑Chloropyridyl Ynones with Nitromethane An approach of general applicability to diverse quinolines and isoquinolines via a tactic that utilizes the recursive anion from nitromethane as a 1C-connector to stitch easily and appropriately crafted pyridyl ynones through a transition-metal-free, tandem Michael addition–S<sub>N</sub>Ar process is delineated. The straightforwardness, one-pot operation, and good yields mark this methodology for wider exploitation in targeting more embellished quinolines and isoquinolines and complex platforms embodying these moieties. moietie;Site-Selective;straightforwardnes;Nitromethane;applicability;1 C-connector;platform;Isoquinoline;methodology;nitromethane;tactic;Chloropyridyl;approach;Synthesi;2-;isoquinoline;tandem;Domino Benzannulation;transition-metal-free;Quinoline;yields mark;anion;Ynone;exploitation;quinoline;one-pot operation;Ar;pyridyl ynones 2019-06-14
    https://acs.figshare.com/articles/dataset/Synthesis_of_Quinolines_and_Isoquinolines_via_Site-Selective_Domino_Benzannulation_of_2-_and_3_Chloropyridyl_Ynones_with_Nitromethane/8321279
10.1021/acs.joc.9b00950.s004