Microwave-Assisted Multi-Component Green Synthesis of Benzo[α]furo[2, 3-c]phenazine Derivatives via a Magnetically-Separable Fe₃O₄@rGO@ZnO-HPA Nanocatalyst under Solvent-Free Conditions

References

• K. Niknam, N. Borazjani, R. Rashidian, and A. Jamali, “Silica-Bonded N-Propylpiperazine Sodium n-Propionate as Recyclable Catalyst for Synthesis of 4H-Pyran Derivatives,” Chinese Journal of Catalysis 34, no. 12 (2013): 2245–54.
   Web of Science ®Google Scholar
• R. V. A. Orru and M. De Greef, “Recent Advances in Solution-Phase Multicomponent Methodology for the Synthesis of Heterocyclic Compounds,” Synthesis 10, no. 10 (2003): 1471–99.
   Google Scholar
• S. L. Schreiber, “Target-Oriented and Diversity-Oriented Organic Synthesis in Drug Discovery,” Science 287, no. 5460 (2000): 1964–9.
   PubMed Web of Science ®Google Scholar
• L. Weber, “The Application of Multi-Component Reactions in Drug Discovery,” Current Medicinal Chemistry 9, no. 23 (2002): 2085–93.
   PubMed Web of Science ®Google Scholar
• I. Akritopoulou-Zanze and S. W. Djuric, “Applications of MCR-Derived Heterocycles in Drug Discovery,” Topics in Heterocyclic Chemistry 25 (2010): 231–87.
   Google Scholar
• A. Nefzi, J. M. Ostresh, and R. A. Houghten, “The Current Status of Heterocyclic Combinatorial Libraries,” Chemical Reviews 97, no. 2 (1997): 449–72.
   PubMed Web of Science ®Google Scholar
• L. A. Thompson, “Recent Applications of Polymer-Supported Reagents and Scavengers in Combinatorial, Parallel, or Multistep Synthesis,” Current Opinion in Chemical Biology 4, no. 3 (2000): 324–37.
   PubMed Web of Science ®Google Scholar
• M. B. Gawande, S. N. Shelke, R. Zboril, and R. S. Varma, “Microwave-Assisted Chemistry: Synthetic Applications for Rapid Assembly of Nanomaterials and Organics,” Accounts of Chemical Research 47, no. 4 (2014): 1338–48.
   PubMed Web of Science ®Google Scholar
• D. Garella, E. Borretto, A. Di. Stilo, K. Martina, G. Cravotto, and P. Cintas, “Microwave-Assisted Synthesis of N-Heterocycles in Medicinal Chemistry,” MedChemComm 4, no. 10 (2013): 1323–43.
   Web of Science ®Google Scholar
• M. A. Zolfigol, “Silica Sulfuric Acid/NaNO2 as a Novel Heterogeneous System for Production of Thionitrites and Disulfides under Mild Conditions,” Tetrahedron 57, no. 46 (2001): 9509–11.
   Web of Science ®Google Scholar
• D. M. Pore, M. S. Soudagar, U. V. Desai, T. S. Thopate, and P. P. Wadagaonkar, “Potassium Phosphate or Silica Sulfuric Acid Catalyzed Conjugate Addition of Thiols to a,b-Unsaturated Ketones at Room Temperature under Solvent-Free Conditions,” Tetrahedron Letters 47, no. 52 (2006): 9325–8.
   Web of Science ®Google Scholar
• S. Minakata and M. Komatsu, “Organic Reactions on Silica in Water,” Chemical Reviews 109, no. 2 (2009): 711–24.
   PubMed Web of Science ®Google Scholar
• P. Salehi, M. A. Zolfigol, F. Shirini, and M. Baghbanzadeh, “Silica Sulfuric Acid and Silica Chloride as Efficient Reagents for Organic Reactions,” Current Organic Chemistry 10, no. 17 (2006): 2171–89.
   Web of Science ®Google Scholar
• K. Niknam, D. Saberi, M. Sadegheyan, and A. Deris, “Silica-Bonded S-Sulfonic Acid: An Efficient and Recyclable Solid Acid Catalyst for the Synthesis of 4,40-(Arylmethylene)Bis(1H-Pyrazol-5-Ols),” Tetrahedron Letters 51, no. 4 (2010): 692–4.
   Web of Science ®Google Scholar
• S. Rostamizadeh, M. Nojavan, R. Aryan, H. Sadeghian, and M. Davoodnejad, “A Novel and Efficient Synthesis of Pyrazolo[3,4-d]Pyrimidine Derivatives and the Study of Their Anti-Bacterial Activity,” Chinese Chemical Letters 24, no. 7 (2013): 629–32.
   Web of Science ®Google Scholar
• J. B. Laursen and J. Nielsen, “Phenazine Natural Products: Biosynthesis, Synthetic Analogues, and Biological Activity,” Chemical Reviews 104, no. 3 (2004): 1663–86.
   PubMed Web of Science ®Google Scholar
• R. Mohebat and A. Yazdani-Elah-Abadi, “Caffeine Catalyzed Green Synthesis of Novel Benzo[a][1,3]Oxazino[6,5-c]Phenazines via a One-Pot Multi-Component Sequential Protocol in a Basic Ionic Liquid,” Chinese Chemical Letters 28, no. 6 (2017): 1340–4.
   Web of Science ®Google Scholar
• D. V. Mavrodi, W. Blankenfeldt, and L. S. Thomashow, “Phenazine Compounds in Fluorescent Pseudomonas Spp. Biosynthesis and Regulation,” Annual Review of Phytopathology 44 (2006): 417–45.
   PubMed Web of Science ®Google Scholar
• D. V. Mavrodi, T. L. Peever, O. V. Mavrodi, J. A. Parejko, J. M. Raaijmakers, P. Lemanceau, S. Mazurier, L. Heide, W. Blankenfeldt, D. M. Weller, et al. “Diversity and Evolution of the Phenazine Biosynthesis Pathway,” Applied and Environmental Microbiology 76, no. 3 (2010): 866–79.
   PubMed Web of Science ®Google Scholar
• S. Nakaike, T. Yamagishi, K. Nanaumi, S. Otomo, and S. Tsukagoshi, “Cell-Killing Activity and Kinetic Analysis of a Novel Antitumor Compound NC-190, a Benzo[a]phenazine Derivative,” Japanese Journal of Cancer Research 83, no. 4 (1992): 402–9.
   PubMedGoogle Scholar
• P. Mistry, A. J. Stewart, W. Dangerfield, M. Baker, C. Liddle, D. Bootle, B. Kofler, D. Laurie, W. A. Denny, B. Baguley, et al. “In Vitro and in Vivo Characterization of XR11576, a Novel, Orally Active, Dual Inhibitor of Topoisomerase I and II,” Anti-Cancer Drugs 13, no. 1 (2002): 15–28.
   PubMed Web of Science ®Google Scholar