One-Pot Multicomponent Synthesis of 2-Amino-4-Aryl-4H-Benzo[h]Chromene Derivatives

References

• G. Singh, A. Sharma, H. Kaur, and M. Ishar, “Chromanyl-Isoxazolidines as Antibacterial Agents: Synthesis, Biological Evaluation, Quantitative Structure Activity Relationship, and Molecular Docking Studies,” Chemical Biology & Drug Design 87 (2016): 213–23.
   PubMed Web of Science ®Google Scholar
• N. D. Vala, H. H. Jardosh, and M. P. Patel, “5-PS-TBD Triggered General Protocol for the Synthesis of 4H-Chromenes, Pyrano[4,3-b]pyran and Pyrano[3,2-c]chromene Derivatives of 1H-Pyrazole and their Biological Activities,” Chinese Chemical Letters 27 (2016): 168–72.
   Web of Science ®Google Scholar
• C. Bingi, N. R. Emmadi, M. Chennapuram, Y. Poornachandra, C. G. Kumar, J. B. Nanubolu, and K. Atmakur, “One-Pot Catalyst Free Synthesis of Novel Kojic Acid Tagged 2-Aryl/alkyl Substituted-4H-Chromenes and Evaluation of their Antimicrobial and Anti-Biofilm,” Bioorganic & Medicinal Chemistry Letters 25 (2015): 1915–19.
   PubMed Web of Science ®Google Scholar
• D. Killander and O. Sterner, “Synthesis of the Bioactive Benzochromenes Pulchrol and Pulchral, Metabolites,” European Journal of Organic Chemistry 8 (2014): 1594–96.
   Web of Science ®Google Scholar
• B. V. S. Reddy, B. Divya, M. Swain, T. P. Rao, J. S. Yadav, M. V. P. S. Vishnu Vardhan, “A Domino Knoevenagel Hetero-Diels-Alder Reaction for the Synthesis of Polycyclic Chromene Derivatives and Evaluation of Their Cytotoxicity,” Bioorganic & Medicinal Chemistry Letters 22 (2012): 1995–99.
   PubMed Web of Science ®Google Scholar
• K. V. Sashidhara, M. Kumar, R. K. Modukuri, A. Srivastava, and A. Puri, “Discovery and Synthesis of Novel Substituted Benzocoumarins as Orally Active Lipid Modulating Agents,” Bioorganic & Medicinal Chemistry Letters 21 (2011): 6709–13.
   PubMed Web of Science ®Google Scholar
• A. A. Fadda, M. A. Berghot, F. A. Amer, D. S. Badawy, and N. M. Bayoumy, “Synthesis and Antioxidant and Antitumor Activity of Novel Pyridine, Chromene, Thiophene and Thiazole Derivatives,” Archives of Pharmaceutical Chemistry 345 (2012): 378–85.
   PubMed Web of Science ®Google Scholar
• N. Jain, J. Xu, R. M. Kanojia, F. Du, G. Jian-Zhong, E. Pacia, M.-T. Lai, A. Musto, G. Allan, M. Reuman, et al., “Identification and Structure-Activity Relationships of Chromene-Derived Selective Estrogen Receptor Modulators for Treatment of Postmenopausal Symptoms,” Journal of Medical Chemistry 52 (2009): 7544–69.
   PubMed Web of Science ®Google Scholar
• A. T. El-Sayed and M. A. Ibrahim, “Synthesis and Antimicrobial Activity of Chromone-linked-2-Pyridone Fused with 1,2,4-Triazoles, 1,2,4-Triazines and 1,2,4-Triazepines Ring Systems,” Journal of the Brazilian Chemical Society 21 (2010): 1007–16.
   Web of Science ®Google Scholar
• M. T. MacDonough, T. E. Strecker, E. Hamel, J. J. Hall, D. J. Chaplin, M. L. Trawick, and K. G. Pinney, “Synthesis and Biological Evaluation of Indole-Based, Anti-Cancer Agents Inspired by the Vascular Disrupting Agent 2-(3'-hydroxy-4'-methoxyphenyl)-3-(3′′,4′′,5′′-trimethoxybenzoyl)-6-methoxyindole (OXi8006),” Bioorganic & Medical Chemistry 21 (2013): 6831–43.
   PubMed Web of Science ®Google Scholar
• C. Kirilmis, M. Ahmedzade, S. Servi, M. Koca, A. Kizirgil, and C. Kazaz, “Synthesis and Antimicrobial Activity of Some Novel Derivatives of Benzofuran: Part 2. The Synthesis and Antimicrobial Activity of Some Novel 1-(1-Benzofuran-2-yl)-2-mesitylethanone Derivatives,” European Journal of Medical Chemistry 43 (2008): 300–8.
   PubMed Web of Science ®Google Scholar
• M. N. Elinson, A. I. Ilovaisky, V. M. Merkulova, P. A. Belyakov, A. O. Chizhov, and G. I. Nikishin, “Solvent-Free Cascade Reaction: Direct Multicomponent Assembling of 2-Amino-4H-Chromene Scaffold from Salicylaldehyde, Malononitrile or Cyanoacetate And Nitroalkanes,” Tetrahedron 66 (2010): 4043–48.
   Web of Science ®Google Scholar
• H. Mehrabi and M. Kazemi-Mireki, “CuO Nanoparticles: An Efficient and Recyclable Nanocatalyst for the Rapid and Green Synthesis of 3,4-Dihydropyrano[c]Chromenes,” Chinese Chemical Letters 22 (2011): 1419–22.
   Web of Science ®Google Scholar
• S. Makarem, A. A. Mohammadi, and A. R. Fakhari, “A Multi-Component Electro-Organic Synthesis of 2-Amino-4H-chromenes,” Tetrahedron Letters 49 (2008): 7194–96.
   Web of Science ®Google Scholar
• M. N. Elinson, A. S. Dorofeev, S. K. Feducovich, R. F. Nasybullin, S. V. Gorbunov, and G. I. Nikishin, “Electrocatalytic Chain Transformation of Salicylaldehydes and Malononitrile into Substituted 4H-Chromenes,” Electrochemistry Communications 8 (2006): 1567–71.
   Web of Science ®Google Scholar
• G. Zbancioc and I. I. Mangalagiu, “Microwave-Assisted Synthesis of Highly Fluorescent Pyrrolopyridazine Derivatives,” Synlett 5 (2006): 804–6.
   Google Scholar
• J. Safari and L. Javadian, “Ultrasound Assisted the Green Synthesis of 2-Amino-4H-Chromene Derivatives Catalyzed by Fe3O4-Functionalized Nanoparticles with Chitosan as a Novel and Reusable Magnetic Catalyst,” Ultrasonics and Sonochemistry 22 (2015): 341–48.
   PubMed Web of Science ®Google Scholar
• S. Caddick and R. Fitzmaurice, “Microwave Enhanced Synthesis,” Tetrahedron 65 (2009): 3325–55.
   Web of Science ®Google Scholar
• C. O. Kappe and D. Dallinger, “The Impact of Microwave Synthesis on Drug Discovery,” Nature Reviews Drug Discovery 5 (2006): 51–63.
   PubMed Web of Science ®Google Scholar
• V. P. Mehta, S. G. Modha, E. Ruijter, K. Van Hecke, L. Van Meervelt, C. Pannecouque, J. Balzarini, R. V. A. Orru, and E. Van der Eycken, “A Microwave-Assisted Diastereoselective Multicomponent Reaction to Access Dibenzo[c,e]azepinones: Synthesis and Biological Evaluation,” Journal of Organic Chemistry 76 (2011): 2828–39.
   PubMed Web of Science ®Google Scholar
• B. Groenendaal, D. J. Vugts, R. F. Schmitz, F. J. J. de Kanter, E. Ruijter, M. B. Groen, and R. V. A. Orru, “A Multicomponent Synthesis of Triazinane Diones,” Journal of Organic Chemistry 73 (2008): 719–22.
   PubMed Web of Science ®Google Scholar
• H. Ren, R. Yu, J. Wang, Q. Jin, M. Yang, D. Mao, D. Kisailus, H. Zhao, and D. Wang, “Multishelled TiO2 Hollow Microspheres as Anodes with Superior Reversible Capacity for Lithium Ion Batteries,” Nano Letters 14 (2014): 6679–84.
   PubMed Web of Science ®Google Scholar
• G. Zbancioc, A. M. Zbancioc, and I. I. Mangalagiu, “Ultrasound and Microwave Assisted Synthesis of Dihydroxyacetophenone Derivatives with or without 1,2-Diazine Skeleton,” Ultrasonics and Sonochemistry 21 (2014): 802–11.
   PubMed Web of Science ®Google Scholar
• S. Shinde, S. Damate, S. Morbale, M. Patil, and S. S. Patil, “Aegle marmelos in Heterocyclization: Greener, Highly Efficient, One-Pot Three-Component Protocol for the Synthesis of Highly Functionalized 4H-Benzochromenes and 4H-Chromenes,” RSC Advances 7 (2017): 7315–28.
   Web of Science ®Google Scholar