DABCO: An Efficient Base Catalyst for a Short and Faster One-Pot Three-Component Synthesis of Highly Functionalized Cyclohexenones: 2-Oxo-N,4,6-triarylcyclohex-3-enecarboxamides

References

• H. Valizadeh and A. Fakhari, “New Multicomponent Approach for the Synthesis of Benzo [c] Coumarin Derivatives over MgO under Solvent-Free Conditions,” Molecular Diversity 15, no. 1 (2011): 233–37.
   PubMed Web of Science ®Google Scholar
• E. Gelens, F. J. De Kanter, R. F. Schmitz, L. A. Sliedregt, B. J. Van Steen, C. G. Kruse, R. Leurs, M. B. Groen, and R. V. Orru, “Efficient Library Synthesis of Imidazoles Using a Multicomponent Reaction and Microwave Irradiation,” Molecular Diversity 10, no. 1 (2006): 17–22.
   PubMed Web of Science ®Google Scholar
• A. Shaabani, A. Maleki, A. H. Rezayan, and A. Sarvary, “Recent Progress of Isocyanide-Based Multicomponent Reactions in Iran,” Molecular Diversity 15, no. 1 (2011): 41–68.
   PubMed Web of Science ®Google Scholar
• X. Xin, Y. Wang, S. Kumar, X. Liu, Y. Lin, and D. Dong, “Efficient One-Pot Synthesis of Substituted Pyridines through Multicomponent Reaction,” Organic & Biomolecular Chemistry 8, no. 13 (2010): 3078–82.
   PubMed Web of Science ®Google Scholar
• H. A. Oskooie, M. M. Heravi, N. Karimi, and G. Kohansal, “Cu/SiO2-Catalyzed One-Pot Synthesis of 12-Aryl-8,9,10,12-tetrahydrobenzo[α]xanthen-11-ones under Solvent-Free Conditions,” Synthetic Communications 41, no. 18 (2011): 2763–68.
   Web of Science ®Google Scholar
• L. Weber, “Multi-Component Reactions and Evolutionary Chemistry,” Drug Discovery Today 7, no. 2 (2002): 143–47.
   PubMed Web of Science ®Google Scholar
• A. Dömling, “Advances in Isocyanide-based Multicomponent Chemistry,” Current Opinion in Chemical Biology 6, no. 3 (2002): 306–13.
   PubMed Web of Science ®Google Scholar
• S. Kanakaraju, B. Prasanna, S. Basavoju, and G. V. P. Chandramouli, “Ammonium Acetate Catalyzed an Efficient One-Pot Three Component Synthesis of Pyrano [3, 2-c] chromene Derivatives,” Arabian Journal of Chemistry 10 (2017): S2705–S13.
   Web of Science ®Google Scholar
• J. Safaei‐Ghomi and Z. Alishahi, “The Preparation of Some Novel Indazole Derivatives by Using Chalcones,” Journal of Fudan University (Natural Science) 44 (2005): 789–90.
   Google Scholar
• C. M. McBride, P. A. Renhowe, C. Heise, J. M. Jansen, G. Lapointe, S. Ma, R. Piñeda, J. Vora, M. Wiesmann, and C. M. Shafer, “Design and Structure–Activity Relationship of 3-benzimidazol-2-yl-1H-indazoles as Inhibitors of Receptor Tyrosine Kinases,” Bioorganic & Medicinal Chemistry Letters 13 (2006): 3595.
   Web of Science ®Google Scholar
• B. C. Kim, J. L. Kim, and Y. U. Jhang, “A Versatile Synthesis of 3-substituted Indazoles,” Bulletin of the Korean Chemical Society 15 (1994): 97; Chemical Abstract 121, (1994): 50097z.
   Web of Science ®Google Scholar
• M. Yamaguchi, N. Maruyama, T. Koga, K. Kamei, M. Akima, T. Kuroki, M. Hamana, and N. Ohi, “Novel Antiasthmatic Agents with Dual Activities of Thromboxane A2 Synthetase Inhibition and Bronchodilation. VI. Indazole Derivatives,”Chemical & Pharmaceutical Bulletin 43, no. 2 (1995): 332–34.
   PubMed Web of Science ®Google Scholar
• D. H. Vyas, S. D. Tala, J. D. Akbari, M. F. Dhaduk, and H. S. Joshi, “Synthesis, Antimicrobial and Antitubercular Activity of Some Cyclohexenone and Indazole Derivatives,” Indian Journal of Chemistry 48B (2009): 1405–10.
   Google Scholar
• V. Gorge, L. De, U. T. Kim, and L. Jing, “Erickson-Viitanen S. Nonsymmetric P2/P2 ‘Cyclic Urea HIV Protease Inhibitors. Structure Activity Relationship, Bioavailability, and Resistance Profile of Monoindazole-Substituted P2 Analogues,” Journal of Medicinal Chemistry 41 (1998): 2411–23.
   PubMed Web of Science ®Google Scholar
• K. Ilango, P. Valentina, and G. Saluja, “Synthesis and in Vitro Anticancer Activity of Some Substituted Chalcones Derivatives,” Research Journal of Pharmaceutical, Biological and Chemical Sciences 1, no. 4 (2010): 354–59.
   Google Scholar
• M. R. Mousavi, M. T. Maghsoodlou, and S. M. Habibi-Khorassani, “One-Pot Diastreoselective Synthesis of Highly Functionalized Cyclohexenones: 2-Oxo-N,4,6-triarylcyclohex-3-enecarboxamides,” Molecular Diversity 18, no. 4 (2014): 821–28.
   PubMed Web of Science ®Google Scholar
• M. R. Mousavi, H. Gharari, M. T. Maghsoodlou, N. Hazeri, P. Dastorani, R. Soria-Martínez, and S. García-Granda, “Diastereoselective and One-Pot Synthesis of Highly Substituted Cyclohexenones Using Claisen-Schmidt Condensation and Michael Addition,” Journal of Chemical Research 39, no. 9 (2015): 509.
   Web of Science ®Google Scholar
• M. R. Mousavi, M. T. Maghsoodlou, and H. Gharari, “Carbonate-Catalyzed Claisen–Schmidt Condensation: One-Pot Synthesis of Highly Functionalized Cyclohexenones under Environmental Conditions,” Research on Chemical Intermediates 42, no. 3 (2016): 2233–46.
   Web of Science ®Google Scholar
• S. R. Mousavi, “Claisen–Schmidt Condensation: Synthesis of (1S, 6R)/(1R, 6S)‐2‐Oxo‐N,4,6‐triarylcyclohex‐3‐enecarboxamide Derivatives with Different Substituents in H2O/EtOH,” Chirality 28, no. 11 (2016): 728–36.
   PubMed Web of Science ®Google Scholar