1082409-91-3Relevant academic research and scientific papers
Heterocycle-heterocycle strategies: (2-nitrophenyl)isoxazole precursors to 4-aminoquinolines, 1 H-indoles, and quinolin-4(1 H)-ones
Coffman, Keith C.,Palazzo, Teresa A.,Hartley, Timothy P.,Fettinger, James C.,Tantillo, Dean J.,Kurth, Mark J.
, p. 2062 - 2065 (2013/06/05)
Reductive heterocycle-heterocycle (heterocycle → heterocycle; H-H) transformations that give 4-aminoquinolines, 3-acylindoles, and quinolin-4(1H)-ones from 2-nitrophenyl substituted isoxazoles are reported. When this methodology is applied to 3,5-, 4,5-,
Regioselective one pot synthesis of 3,3′-diindolylethylene derivatives and study of their cytotoxic activity
Mandal, Madhumita,Kumar, Deepak,Roy, Rajneeta,Sen, Rupashree,Das, Padma,Chatterjee, Mitali,Jaisankar, Parasuraman
supporting information; experimental part, p. 3084 - 3087 (2011/06/24)
2,2′-Diphenyl-3,3′-diindolylethylene (DPDIE) derivatives 3a-g were regioselectively prepared in one pot from indoles 1a-g in the presence of Lewis acids and were subsequently evaluated for cytotoxic activity against human leukemic cell lines, U937 and K56
