Bulletin of the Korean Chemical Society

  • 제32권11호
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  • Pages.3853-3854
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  • 2011
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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CuO Nanoparticles as an Efficient and Reusable Catalyst for the One-pot Friedlander Quinoline Synthesis

  • Nezhad, Jafar Mohammad (Chemistry Department, Shahre Ghods Branch, Islamic Azad University) ;
  • Akbari, Jafar (Chemistry Department, Buinzahra Branch, Islamic Azad University) ;
  • Heydari, Akbar (Research Center for Organic Chemical Synthesis) ;
  • Alirezapour, Behrooz (Nuclear Medicine Research Group, Agricultural, Medical and Industrial Research School (AMIRS), Nuclear Science and Technology Institute)
  • 투고 : 2011.08.23
  • 심사 : 2011.09.21
  • 발행 : 2011.11.20
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참고문헌

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  1. Copper Based Nanoparticles-Catalyzed Organic Transformations vol.17, pp.3-4, 2013, https://doi.org/10.1007/s10563-013-9159-2
  2. Function of Nanocatalyst in Chemistry of Organic Compounds Revolution: An Overview vol.2013, pp.1687-4129, 2013, https://doi.org/10.1155/2013/341015
  3. Nickel nanoparticles: a highly efficient and retrievable catalyst for the solventless Friedlander annulation of quinolines and their in silico molecular docking studies as histone deacetylase inhibitors vol.5, pp.57, 2015, https://doi.org/10.1039/C5RA06593C
  4. Imidazole-functionalized magnetic Fe3O4 nanoparticles: an efficient, green, recyclable catalyst for one-pot Friedländer quinoline synthesis vol.42, pp.6, 2016, https://doi.org/10.1007/s11164-015-2411-9
  5. Recyclable nano copper oxide catalyzed synthesis of quinoline-2,3-dicarboxylates under ligand free conditions vol.4, pp.29, 2011, https://doi.org/10.1039/c3ra47212d
  6. An environmentally benign, simple and proficient synthesis of quinoline derivatives catalyzed by FeCl3.6H2O as a green and readily available catalyst vol.14, pp.1, 2021, https://doi.org/10.1080/17518253.2020.1869840
  7. NH 4 CL /Zn powder: An efficient, chemoselective reducing catalyst for the microwave‐assisted synthesis of 2,3‐disubstituted quinolines via tandem Knoevenagel condensati vol.58, pp.2, 2011, https://doi.org/10.1002/jhet.4203