78631-18-2Relevant academic research and scientific papers
Synthesis of 2-Acyl- and 2-Benzoylindoles
Mali, Raghao S.,Tilve, Santosh G.,Desai, Vidya G.
, p. 150 - 158 (2007/10/03)
2-Nitrobenzaldehydes (3a-c) on reaction with phosphoranes (4a and 4b), and triphenyl phosphine in refluxing diphenylether provide 2-acylindoles (6a-c) and 2-benzoylindoles (6d-f). Alternatively 2-nitrobenzaldehydes (3a-c) on reaction with phosphoranes (4a and 4b) give nitroketones (5a-f) which on refluxing with triphenyl phosphine in refluxing diphenyl ether furnish 2-acyl- and 2-benzoylindoles (6a-f).
Preparation, reduction chimique et electrochimique d'α-nitrostyrylcetones - synthese d'heterocycles azotes
Marcot, Bernard,Rabaron, Alain,Viel, Claude,Bellec, Christian,Deswarte, Stephane,Maitte, Pierre
, p. 1224 - 1234 (2007/10/02)
Nitration of styryl ketones with nitrogen peroxide leads to the corresponding α-nitroethylenic ketones in good yield.However, the presence of methoxy groups involves a nitration on the aromatic nucleus.LiAlH4 reduction of α-nitrostyrylketones yields the c
