%0 Generic %A Beesu, Mallesh %A Mehta, Goverdhan %D 2019 %T Synthesis of Quinolines and Isoquinolines via Site-Selective, Domino Benzannulation of 2- and 3‑Chloropyridyl Ynones with Nitromethane %U https://acs.figshare.com/articles/dataset/Synthesis_of_Quinolines_and_Isoquinolines_via_Site-Selective_Domino_Benzannulation_of_2-_and_3_Chloropyridyl_Ynones_with_Nitromethane/8321276 %R 10.1021/acs.joc.9b00950.s003 %2 https://acs.figshare.com/ndownloader/files/15593936 %K moietie %K Site-Selective %K straightforwardnes %K Nitromethane %K applicability %K 1 C-connector %K platform %K Isoquinoline %K methodology %K nitromethane %K tactic %K Chloropyridyl %K approach %K Synthesi %K 2- %K isoquinoline %K tandem %K Domino Benzannulation %K transition-metal-free %K Quinoline %K yields mark %K anion %K Ynone %K exploitation %K quinoline %K one-pot operation %K Ar %K pyridyl ynones %X 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–SNAr 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. %I ACS Publications