2017
DOI: 10.1007/s00044-016-1775-8
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Diverse C-6 substituted 4-methyl-2-(2-, 3- and 4-pyridinyl)quinolines: synthesis, in vitro anticancer evaluation and in silico studies

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Cited by 7 publications
(7 citation statements)
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“…( Hey and Williams, 1950 , Nunn and Schofield, 1952 ; Kouznetsov et al., 2012 , 2017 ; Yamaguchi et al., 2016 ; Pang et al., 2017 ; Zhang et al., 2017a , 2017b ; Roder et al., 2019 ) yellow solid was obtained by column chromatography (eluent: EtOAc/petroleum ether = 1/4) with 58% isolated yield (30.0 mg). m. p. = 128-130°C.…”
Section: Methodsmentioning
confidence: 99%
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“…( Hey and Williams, 1950 , Nunn and Schofield, 1952 ; Kouznetsov et al., 2012 , 2017 ; Yamaguchi et al., 2016 ; Pang et al., 2017 ; Zhang et al., 2017a , 2017b ; Roder et al., 2019 ) yellow solid was obtained by column chromatography (eluent: EtOAc/petroleum ether = 1/4) with 58% isolated yield (30.0 mg). m. p. = 128-130°C.…”
Section: Methodsmentioning
confidence: 99%
“…( Hey and Williams, 1950 , Nunn and Schofield, 1952 ; Kouznetsov et al., 2012 , 2017 ; Yamaguchi et al., 2016 ; Pang et al., 2017 ; Zhang et al., 2017a , 2017b ; Roder et al., 2019 ) yellow oil was obtained by column chromatography (eluent: EtOAc/petroleum ether = 1/4) with 46% isolated yield (25.3 mg). 1 H NMR (500 MHz, CDCl 3 ) δ 8.74 (d, J = 4.1 Hz, 1H), 8.65 (d, J = 7.9 Hz, 1H), 8.40 (s, 1H), 8.19 (d, J = 8.5 Hz, 1H), 8.04 (d, J = 8.2 Hz, 1H), 7.88 (t, J = 7.7 Hz, 1H), 7.73 (t, J = 7.6 Hz, 1H), 7.58 (t, J = 7.5 Hz, 1H), 7.36 (t, J = 6.2 Hz, 1H), 2.80 (s, 3H).…”
Section: Methodsmentioning
confidence: 99%
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“…In the literature, there are few reported procedures [ 45 , 46 ] for the CPA ligand synthesis, but herein, we have modified the synthetic procedure for better yield. A mixture of the appropriately Pyridine-4-carbaldehyde (5 mmol) and the appropriately substituted aniline (5 mmol) in dry toluene (50 mL) is refluxed for 5 h in the presence of molecular sieves (75 g; Davison, grade 514Å, effective pore size 4, 8–12 mesh beads).…”
Section: Methodsmentioning
confidence: 99%
“…Finally, supramolecular complexes were prepared by mixing equimolar ratios of a particular Schiff base with the para-alkoxy benzoic acid and then subjected to melting to ensure the formation of the complexes (see Scheme 2). The compounds were identified by their reported melting points: A (98 C) (Boyer et al, 2007), B (100 C) (Poronik et al, 2017), C (88 C) (Kouznetsov et al, 2017), D (74 C) (Krishna Murthy et al, 2018), E (80 C) (Boyer et al, 2007), and F (82 C).…”
Section: Methodsmentioning
confidence: 99%