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Articles

SiO2-BiCl3 as Heterogeneous Catalyzed Synthesis of 6-Methyl-2-aryl-4,5-dihydropyridazin-3(2H)-one Derivatives

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Pages 1501-1509 | Received 27 Sep 2018, Accepted 06 Dec 2018, Published online: 15 Feb 2019

References

  • B. S. Kwak, “Applications of Heterogeneous Catalystic Processes to the Environmentally Friendly Synthesis of Chemicals,” Catalysis Surveys from Asia 9, no. 2 (2005): 103–16.
  • M. J. Climent, A. Corma, and S. Iborra, “Heterogeneous Catalysts for the One-Pot Synthesis of Chemicals and Fine Chemicals,” Chemical Reviews 111, no. 2 (2011): 1072–133.
  • A. Corma, “Inorganic Solid Acids and Their Use in Acid-Catalyzed Hydrocarbon Reactions,” Chemical Reviews 95, no. 3 (1995): 559–614.
  • K. Wilson and J. H. Clark, “Solid Acids and Their Use as Environmentally Friendly Catalysts in Organic Synthesis,” Pure and Applied Chemistry 72, no. 7 (2000): 1313–19.
  • T. Okuhara, “Water-Tolerant Solid Acid Catalysts,” Chemical Reviews 102, no. 10 (2002): 3641–66.
  • J. H. Clark, “Solid Acids for Green Chemistry,” Accounts of Chemical Research 35, no. 9 (2002): 791–97.
  • A. Corma and H. Garcia, “Lewis Acids: From Conventional Homogeneous to Green Homogeneous and Heterogeneous Catalysis,” Chemical Reviews 103, no. 11 (2003): 4307–66.
  • G. Sartori, R. Ballini, F. Bigi, G. Bosica, R. Maggi, and P. Righi, “Protection (and Deprotection) of Functional Groups in Organic Synthesis by Heterogeneous Catalysis,” Chemical Reviews 104, no. 1 (2004): 199–250.
  • M. Postel and E. Duñach, “Bismuth Derivatives for the Oxidation of Organic Compounds,” Coordination Chemical Reviews 155 (1996): 127–44.
  • H. Suzuki, T. Ikegami, and Y. Matano, “Bismuth in Organic Transformations,” Synthesis 3, no. 3 (1997): 249–67.
  • N. M. Leonard, L. C. Wieland, and R. S. Mohan, “Applications of Bismuth(III) Compounds in Organic Synthsis,”Tetrahedron 58, no. 42 (2002): 8373–97.
  • C. Le Roux, J. Dubac, “Bismuth(III) Chloride and Triflate: Novel Catalysts for Acylation and Sulfonylation Reactions: Survey and Mechanistic Aspects,” Synlett 2 (2002): 181–200.
  • H. Gaspard-Iloughmane and C. Le Roux, “Bismuth(III) Triflate in Organic Synthesis,” European Journal of Organic Chemistry 12 (2004): 2517–32.
  • H. Gaspard-Iloughmane and C. Le Roux, “Recent Advances in the Use of Bismuth(III) Triflate in Organic Synthesis: An Update,” Trends in Organic Chemistry 11 (2006): 65–80.
  • R. Hua, “Recent Advances in Bismuth-Catalyzed Organic Synthesis,” Current Organic Synthesis 5, no. 1 (2008): 1–27.
  • J. M. Bothwell, S. W. Krabbe, and R. S. Mohan, “Applications of Bismuth(III) Compounds in Organic Synthesis,” Chemical Society Reviews 40, no. 9 (2011): 4649–707.
  • K. Aghapoor, L. Ebadi-Nia, F. Mohsenzadeh, M. Mohebi Morad, Y. Balavar, and H. R. Darabi, “Silica-Supported Bismuth(III) Chloride as a New Recyclable Heterogeneous Catalyst for the Paal-Knorr Pyrrole Synthesis,” Journal of Organometallic Chemistry 708 (2012): 25–30.
  • E. Ruijter, R. Scheffelaar, and R. V. A. Orru, “Multicomponent Reaction Design in the Quest for Molecular Complexity and Diversity,” Angewandte Chemie International Edition 50, no. 28 (2011): 6234–46.
  • B. Ganem, “Strategies for Innovation in Multicomponent Reaction Design,” Accounts of Chemical Research 42, no. 3 (2009): 463–72.
  • L. El Kaïm and L. Grimaud, “Ugi-Smiles Couplings: New Entries to N-Aryl Carboxamide Derivatives,” Molecular Diversity 14, no. 4 (2010): 855–67.
  • M. Tisler and B. Stanovnlk, “Synthesis of Pyridazine Derivatives-XIII: Formation of Some Substituted Imidazo (1.2-b) Pyridazines.” Tetrahedron 23 (1967): 2739–2746.
  • T. Eicher and S. Hauptmann, The Chemistry of Heterocycles: Structure, Reactions, Syntheses, and Applications (Wiley-VCH, 2003), 7206.
  • A. Husain, A. Ahmad, A. Bhandari, and V. Ram, “Synthesis and Antitubercular Activity of Pyridazinone Derivatives,” Journal of the Chilean Chemical Society 56, no. 3 (2011): 778–81.
  • M. Asif, “General Study of Pyridazine Compounds against Cyclooxygenase Enzyme and Their Relation with Analgesic, Anti-inflammatory and anti-Arthritic Activities,” Chronicles of Young Scientist 1 (2010): 3–9.
  • M. S. R. Murty, B. Ramalingeswara Rao, K. R. Ram, J. S. Yadav, J. Antony, and R. J. Anto, “Synthesis and Preliminary Evaluation Activity Studies of Novel 4-(Aryl/heteroaryl-2-ylmethyl)-6-phenyl-2-[3-(4-substituted-piperazine-1-yl)propyl]pyridazin-3(2H)-One Derivatives as Anticancer Agents,” Medicinal Chemistry Research 21, no. 10 (2012): 3161–69.
  • M. Asif and A. Singh, “Exploring Potential, Synthetic Methods and General Chemistry of Pyridazine and Pyridazinone: A Brief Introduction,” International Journal of Chemical Technical Research 2 (2010): 1112–28.
  • T. Costas, P. Besada, A. Piras, L. Acevedo, M. Yañez, F. Orallo, R. Laguna, and C. Terán, “New Pyridazinone Derivatives with Vasorelaxant and Platelet Antiaggregatory Activities,” Bioorganic Medicinal Chemistry Letters 20, no. 22 (2010): 6624–27.
  • M. Asif, S. Deewan, and S. Anita, “Analgesic Activity of Some 6-Phenyl-4-Substituted Benzylidene Tetrahydro Pyridazin-3(2H)-Ones,” Global Journal of Pharmacology 5 (2011): 18–22.
  • M. Asif and S. Anita, “Anticonvulsant Activity of 4-(Substituted Benzylidene)-6-(3-nitrophenyl)-4,5-dihydroPyridazin-3(2H)-Ones Against Maximal Electro Shock Induced Seizure,” Middle-East Journal of Scientific Research 9 (2011): 481–85.
  • S. Seth, A. Sharma, and D. Raj, “Pyridazinones: A Monder Nucleus with Scaffold of Pharmacological Activities,” American Journal of Biological and Pharmaceutical Research 1 (2014): 105–16.
  • G. Toth, S. Molnar, T. Tamas, and I. Borbely, “An Efficient Synthesis of 4,5-Dihydro-3(2H)-Pyridazinone Derivatives,” Synthetic Communications 27 (1997): 3513–23.
  • K. Alex, A. Tillack, N. Schwarz, and M. Beller, “First Synthesis of 4,5-dihydro-3(2H)-Pyridazinones via Zn-Mediated Hydrohydrazination,”Tetrahedron Letters 49, no. 31 (2008): 4607–09.
  • A. Albrecht, J. Koszuk, M. Kobuciński, and T. Janecki, “New, Simple and Versatile Synthesis of 4,6-Disubstituted Pyridazin-3(2H)-Ones,” Organic & Biomolecular Chemistry 6, no. 7 (2008): 1197–200.
  • K. Aghapor, L. Ebadi-Nia, F. Mohsenzadeh, M. W. Morad, Y. Balavar, and H. R. Darabi, “Silica-Supported Bismuth(III) Chloride as a New Recyclable Heterogeneous Catalyst for the Paal–Knorr Pyrrole Synthesis,” Journal of Organic Chemistry 708 (2012): 25–30.

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