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Molecules 2002, 7(8), 618-627; doi:10.3390/70800618

Synthesis of Substituted 2-Pyridyl-4-phenylquinolines

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Received: 21 June 2002 / Revised: 2 August 2002 / Accepted: 3 August 2003 / Published: 31 August 2002
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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.
Keywords: Quinoline derivatives; asymmetric bidentate aza-ligands; 2D-NMR Quinoline derivatives; asymmetric bidentate aza-ligands; 2D-NMR
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MDPI and ACS Style

Mamo, A.; Nicoletti, S.; Tat, N.C. Synthesis of Substituted 2-Pyridyl-4-phenylquinolines. Molecules 2002, 7, 618-627.

AMA Style

Mamo A, Nicoletti S, Tat NC. Synthesis of Substituted 2-Pyridyl-4-phenylquinolines. Molecules. 2002; 7(8):618-627.

Chicago/Turabian Style

Mamo, Antonino; Nicoletti, Salvatore; Tat, N. C. 2002. "Synthesis of Substituted 2-Pyridyl-4-phenylquinolines." Molecules 7, no. 8: 618-627.

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