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Articles

Nano-CuFe2O4@SO3H Catalyzed Efficient One-Pot Cyclo-Dehydration of Dimedone and Synthesis of Chromeno[4,3-b]chromenes

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Pages 111-123 | Received 09 Sep 2016, Accepted 06 Jan 2017, Published online: 02 Feb 2017

References

  • Mokhtary, M. “Recent advances in catalysts immobilized on magnetic nanoparticles.” Journal of the Iranian Chemical Socitey 13 (2016): 1827–45.
  • Jiao, H., G. S. Jiao, and J. L. Wang. “Preparation and magnetic properties of CuFe2O4 nanoparticles.” Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry, 43 (2013): 131–4.
  • Parella, R., N. A. Kumar, and S. A. Babu. “Catalytic Friedel–Crafts acylation: magnetic nanopowder CuFe2O4 as an efficient and magnetically separable catalyst.” Tetrahedron Letters 54 (2013): 1738–42.
  • Kassaee, M. Z., H. Masrouri, and F. Movahedi. “Sulfamic acid-functionalized magnetic Fe3O4 nanoparticles as an efficient and reusable catalyst for one-pot synthesis of α-amino nitriles in water.” Appled Catalysis A: General 395 (2011): 28–33.
  • Khan, K. M., G. M. Maharvi, M. T. H. Khan, A. J. Shaikh, S. Perveen, S. B. Mild, and M. I. Choudhary. “Tetraketones: A new class of tyrosinase inhibitors.” Bioorganic & Medicinal Chemistry 14 (2006): 344–51.
  • Maharvi, G. M., S. Ali, N. Riaz, N. Afza, A. Malik, M. Ashraf, L. Iqbal, and M. Lateef. “Mild and efficient synthesis of new tetraketones as lipoxygenase inhibitors and antioxidants.” Journal of Enzyme Inhibition and Medicinal Chemistry 23 (2008): 62–9.
  • Sirkecioglu, O., N. Talinli, and A. Akar. “Synthesis of 14-alkyl-14H-dibenzo[a,j]xanthenes.” Journal of Chemical Research (1995): 502–6.
  • Ilangovan, A., S. Malayappasamy, S. Muralidharan, and S. Maruthamuthu. “A highly efficient green synthesis of 1, 8-dioxo-octahydroxanthenes.” Chemistry Central Journal 5 (2011): 81–6.
  • Kantevari, S., R. Bantu, and L. Nagarapu. “HClO4–SiO2 and PPA–SiO2 catalyzed efficient one-pot Knoevenagel condensation, Michael addition and cyclo-dehydration of dimedone and aldehydes in acetonitrile, aqueous and solvent free conditions: Scope and limitations.” Journal of Molecular Catalysis A: Chemical 269 (2007): 53–7.
  • Tong-Shou, J., J. S. Zhang, A. Q. Wang, and T. S. Li. “Ultrasound-assisted synthesis of 1,8-dioxo-octahydroxanthene derivatives catalyzed by p-dodecylbenzenesulfonic acid in aqueous media.” Ultrasonics Sonochemistry 13 (2006): 220–4.
  • Mahdavinia, G. H., M. A. Bigdeli, and Y. S. Hayeniaz. “Covalently anchored sulfonic acid on silica gel (SiO2-R-SO3H) as an efficient and reusable heterogeneous catalyst for the one-pot synthesis of 1,8-dioxo-octahydroxanthenes under solvent-free conditions.” Chinese Chemical Letters 20 (2009): 539–41.
  • Li, J. T., Y. W. Li, Y. L. Song, and G. F. Chen. “Improved synthesis of 2,2′-arylmethylene bis(3-hydroxy-5,5-dimethyl-2-cyclohexene-1-one) derivatives catalyzed by urea under ultrasound.” Ultrasonics Sonochemistry 19 (2012): 1–4.
  • Dadhania, A. N., V. K. Patel, and D. K. Raval. “Catalyst-free sonochemical synthesis of 1,8-dioxo-octahydroxanthene derivatives in carboxy functionalized ionic liquid.” Comptes Rendus Chimie 15 (2012): 378–83.
  • Mokhtary, M., and S. A. Mirfarjood Langroudi. “Polyvinylpolypyrrolidone-supported boron trifluoride: A mild and efficient catalyst for the synthesis of 1,8-dioxooctahydroxanthenes and 1,8-dioxodecahydroacridines.” Monatshefte für Chemie 145 (2014): 1489–94.
  • Gesson, J. P., N. Fonteneau, M. Mondon, S. Charbit, H. Ficheux, and F. Schutze. “7-carboxy-flavone derivatives preparation method and therapeutic use.” US Patent 6 (2005): 965, 039 B2.
  • Chen, Z., Q. Zhu, and W. Su. “A novel sulfonic acid functionalized ionic liquid catalyzed multicomponent synthesis of 10,11-dihydrochromeno[4,3-b]chromene-6,8(7H,9H)-dione derivatives in water.” Tetrahedron Letters 52 (2011): 2601–4.
  • Sun, X. J., J. F. Zhou, and S. J. Zhi. “Efficient one-pot synthesis of tetrahydrobenzo [c]xanthene-1,11-dione derivatives under microwave irradiation.” Synthetic Communications 42 (2012): 1987–94.
  • Anaraki-Ardakani, H., R. Ghanavatian, and M. Akbari. “An efficient one-pot Synthesis of tetrahydro-chromeno [4,3-b] chromene-6,8-dione and tetrahydro-pyrano [4,3-b]chromene-1,9-dione derivatives under solvent-free conditions.” World Applied Sciences Journal 22 (2013): 802–8.
  • Pradhan, K., S. Paul, and A. R. Das. “Fe(DS)3, an efficient Lewis acid-surfactant-combined catalyst (LASC) for the one pot synthesis of chromeno[4,3-b]chromene derivatives by assembling the basic building blocks.” Tetrahedron Letters 54 (2013): 3105–10.
  • Nemati, F., A. Elhampour, M. B. Natanzi, and S. Sabaqian. “Nano-CuFe2O4-supported sulfonic acid as a novel and recyclable nanomagnetic acid for diazotization of aromatic amines: efficient synthesis of various azo dyes.” Journal of Iranian Chemical Society 13 (2016): 1045–54.
  • Mokhtary, M., and Torabi, M. “Nano magnetite (Fe3O4), an efficient and robust catalyst for the one-pot synthesis of 1-(aryl(piperidin-1-yl)methyl)naphthalene-2-ol and 1-(a-amido alkyl)-2-naphthol under ultrasound irradiation.” Journal of Saudi Chemical Society in press, doi: 10.1016/j.jscs.2014.03.009.
  • Azgomi, N., and M. Mokhtary. “Nano-Fe3O4@SiO2 supported ionic liquid as an efficient catalyst forthe synthesis of 1,3-thiazolidin-4-ones under solvent-free conditions.” Journal of Molecular Catalysis A: Chemical 398 (2015): 58–64.
  • Baghbanian, S. M., and M. Farhang. “CuFe2O4 nanoparticles: a magnetically recoverable and reusable catalyst for the synthesis of quinoline and quinazoline derivatives in aqueous media.” RSC Advances 4 (2014): 11624–33.
  • Saha, M., K. Pradhan, and A. R. Das. “Facile and eco-friendly synthesis of chromeno[4,3-b]pyrrol-4(1H)-one derivatives applying magnetically recoverable nano crystalline CuFe2O4 involving a domino three-component reaction in aqueous media.” RSC Advances 6 (2016): 55033–38.
  • Rajput, J. K., P. Arora, G. Kaur, and M. Kaur. “CuFe2O4 magnetic heterogeneous nanocatalyst: Low power sonochemical-coprecipitation preparation and applications in synthesis of 4H-chromene-3-carbonitrile scaffolds.” Ultrasonics Sonochemistry 26 (2015): 229–40.

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