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• W2110672212 abstract "The acid-catalyzed condensation of o-aminobenzophenones with aromatic acetyl derivatives, in a basic methanol/tetrahydrofuran medium, has been used to prepare a series of substituted 2-pyridyl-4-phenylquinolines. Derivatives having two aza binding sites can act as asymmetric bidendate ligands to complex transition metals such as ruthenium, osmium or iridium. All the compounds were characterized by elemental analysis, Ei or FAB (+) MS, 1H- and 13C-NMR spectroscopies. Complete assignments of the 1H spectra were accomplished by using a combination of one- and two-dimensional NMR techniques." @default.
• W2110672212 created "2016-06-24" @default.
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• W2110672212 date "2002-08-31" @default.
• W2110672212 modified "2023-10-03" @default.
• W2110672212 title "Synthesis of Substituted 2-Pyridyl-4-phenylquinolines" @default.
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• W2110672212 doi "https://doi.org/10.3390/70800618" @default.
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