References
- X. Gao, L. Cen, F. Li, R. Wen, H. Yan, H. Yao, and S. Zhu, “Oral Administration of Indole Substituted Dipyrido[2,3-d]Pyrimidinederivative Exhibits anti-Tumor Activity via Inhibiting AKT and ERK1/2on Hepatocellular Carcinoma,” Biochemical and Biophysical Research Communications 505 (2018): 1–7. doi:https://doi.org/10.1016/j.bbrc.2018.09.120
- P. Jahanshahi, M. Mamaghani, F. Haghbin, R. Hossein Nia, and M. Rassa, “One-Pot Chemoselective Synthesis of Novel Pyrrole-Substituted Pyrido[2,3-d]Pyrimidines Using [γ-Fe2O3@HAp-SO3H] as an Efficient Nanocatalyst,” Journal of Molecular Structure 1155 (2018): 520–9. doi:https://doi.org/10.1016/j.molstruc.2017.11.034
- R. Naresh Kumar, G. Jitender Dev, N. Ravikumar, D. Krishna Swaroop, B. Debanjan, G. Bharath, B. Narsaiah, S. Nishant Jain, and A. Gangagni Rao, “Synthesis of Novel Triazole/Isoxazole Functionalized 7-(Trifluoromethyl)Pyrido[2,3-d]Pyrimidine Derivatives as Promising Anticancer and Antibacterial Agents,” Bioorganic & Medicinal Chemistry Letters 26, no. 12 (2016): 2927–30. doi:https://doi.org/10.1016/j.bmcl.2016.04.038
- B. Hurlbert and B. Valenti, “Studies on Condensed Pyrimidine Systems. XXIV. The Condensation of 2,4,6-Triaminopyrimidine with Malondialdehyde Derivatives,” Journal of Medicinal Chemistry 11, no. 4 (1968): 708–10. doi:https://doi.org/10.1021/jm00310a016
- A. B. A. El-Gazzar and H. N. Hafez, “Synthesis of 4-Substituted Pyrido[2,3-d]Pyrimidin-4(1H)-One as Analgesic and anti-Inflammatory Agents,” Bioorganic & Medicinal Chemistry Letters 19, no. 13 (2009): 3392–7. doi:https://doi.org/10.1016/j.bmcl.2009.05.044
- D. Heber, C. Heers, and U. Ravens, “Positive Inotropic Activity of 5-Amino-6-Cyano-1,3-Dimethyl-1,2,3,4-Tetrahydropyrido[2,3-d]Pyrimidine-2,4-Dione in Cardiac Muscle from guinea-Pig and Man. Part 6: Compounds with Positive Inotropic Activity,” Die Pharmazie 48, no. 7 (1993): 537–41.
- J. R. Piper, G. S. McCaleb, J. A. Montgomery, R. L. Kisliuk, Y. Gaumont, and F. M. Sirotnak, “Syntheses and Antifolate Activity of 5-Methyl-5-Deaza Analogues of Aminopterin, Methotrexate, Folic Acid, and N10-Methylfolic Acid,” Journal of Medicinal Chemistry 29, no. 6 (1986): 1080–7. doi:https://doi.org/10.1021/jm00156a029
- J. Quiroga, C. Cisneros, B. Insuasty, R. Abonia, S. Cruz, M. Nogueras, J. M. Torre, M. Sortino, and S. Zacchino, “Microwave-Assisted Three-Component Synthesis and in Vitro Antifungal Evaluation of 6-Cyano-5,8-Dihydropyrido[2,3-d]Pyrimidin-4(3H)-Ones,” Journal of Heterocyclic Chemistry 43, no. 2 (2006): 299–306. doi:https://doi.org/10.1002/jhet.5570430208
- J. W. Ellingboe, “Substituted Pyridopyrimidines and Antihyperintensives” (US Patent 5,466,692, 1996). Chem Abstr 124:176134.
- K. Rana, B. Kaur, and B. Kumar, “Synthesis and anti-Hypertensive Activity of Some Dihydropyrimidines,” Indian Journal of Chemistry 43B, (2004): 1553–7.
- M. Ghorab and A. Hassan, “Synthesis and Antibacterial Properties of New Dithienyl Containing Pyran, Pyrano[2,3-b]Pyridine, Pyrano[2,3-d]Pyrimidine and Pyridine Derivatives.” Phosphorus, Sulfur and Silicon and the Related Elements 141, no. 1 (1998): 251–61. doi:https://doi.org/10.1080/10426509808033737.
- V. Furuya and T. Ohtaki, “Pyrido[2,3-d]Pyrimidines and Their Use as Endothelin Antagonists” (Eur Pat EP 608565 A1, Aug 3, 1994). Chem Abstr 121:205395.
- Kurosh Rad-Moghadam and Leila Youseftabar-Miri, “Tetramethylguanidinium Triflate: An Efficient Catalyst Solvent for the Convergent Synthesis of Fused Spiro[1,4-Dihydropyridine-Oxindole] Compounds,” Journal of Fluorine Chemistry. 135 (2012): 213–9. doi:https://doi.org/10.1016/j.jfluchem.2011.11.007
- N. K. Satti, K. A. Suri, O. P. Sun, and A. Kapil, “Synthesis and Antileishmanial Activity of Some Pyrido (1,2-a)Pyrimidines and Phenanthrolines,” Indian Journal of Chemistry Section B: Organic Chemistry Including Medicinal Chemistry 24 (1993): 978–81.
- A. Rosowsky, C. E. Mota, and S. F. Queener, “Synthesis and Antifolate Activity of 2,4-Diamino-5,6,7,8-Tetrahydropyrido[4,3-d]Pyrimidine Analogues of Trimetrexate and Piritrexim,” Journal of Heterocyclic Chemistry 32, no. 1 (1995): 335–40. doi:https://doi.org/10.1002/jhet.5570320155
- O. G. Jolodar, F. Shirini, and M. Seddighi, “Efficient Synthesis of Pyrano[2,3-d]Pyrimidinone and Pyrido[2,3-d]Pyrimidine Derivatives in Presence of Novel Basic Ionic Liquid Catalyst,” Chinese Journal of Catalysis 38, no. 7 (2017): 1245–51. doi:https://doi.org/10.1016/S1872-2067(17)628274
- M. Kidwai, A. Jain, and S. Bhardwaj, “Magnetic Nanoparticles Catalyzed Synthesis of Diverse N-Heterocycles,” Molecular Diversity 16, no. 1 (2012): 121–8. doi:https://doi.org/10.1007/s11030-011-9336-z
- A. M. Rad, and M. Mokhtary, “Efficient One-Pot Synthesis of Pyrido[2,3-d]Pyrimidines Catalyzed by Nanocrystalline MgO in Water,” International Nano Letters 5, no. 2 (2015): 109–23. doi:https://doi.org/10.1007/s40089-015-0145-8.
- B. Sabour, M. H. Peyrovi, and M. Hajimohammadi, “Al-HMS-20 Catalyzed Synthesis of Pyrano[2,3-d]Pyrimidines and Pyrido[2,3-d]Pyrimidines via Three-Component Reaction,” Research on Chemical Intermediates 41, no. 3 (2015): 1343–50. doi:https://doi.org/10.1007/s11164-013-1277-y
- P. Bhattacharyya, S. Paul, and A. R. Das, “Facile Synthesis of Pyridopyrimidine and Coumarin Fused Pyridine Libraries over a Lewis Base-Surfactant-Combined Catalyst TEOA in Aqueous Medium,” RSC Advances 3, no. 10 (2013): 3203–8. doi:https://doi.org/10.1039/c3ra23254a
- S. Abdolmohammadi and S. Balalaie, “A Clean Procedure for Synthesis of pyrido[d]pyrimidine derivatives under solvent-free conditions catalyzed by ZrO(2) nanoparticles,” Combinatorial Chemistry & High Throughput Screening 15, no. 5 (2012): 395–9. doi:https://doi.org/10.2174/138620712800194486
- P. S. Naidu, P. Borah, and P. J. Bhuyan, “Synthesis of Some Novel Functionalized Dihydropyrido[2,3-d]Pyrimidines via an One-Pot Three-Component Reaction Catalysed by InCl3,” Tetrahedron Letters 53no. 31 (2012): 4015–7.
- J. P. Brand, J. Charpentier, and J. Waser, “Direct Alkynylation of Indole and Pyrrole Heterocycles,” Angewandte Chemie (International ed. in English) 48, no. 49 (2009): 9346–9 . doi:https://doi.org/10.1002/anie.200905419
- M. Inman and Ch J. Moody, “Indole Synthesis–Something Old, Something New,” Chemical Science 4, no. 1 (2013): 29–41. doi:https://doi.org/10.1039/C2SC21185H
- M. Z. Zhang, Q. Chen, and G. F. Yang, “A Review on Recent Developments of Indole-Containing Antiviral Agents,” European Journal of Medicinal Chemistry 89, (2015): 421–41. doi:https://doi.org/10.1016/j.ejmech.2014.10.065.
- H. Fan, J. Peng, M. T. Hamann, and J. F. Hu, “Lamellarins and Related Pyrrole-Derived Alkaloids from Marine Organisms,” Chemical Reviews 108, no. 1 (2008): 264–87. doi:https://doi.org/10.1021/cr078199m.
- F. Del Monte, M. Morales, D. Levy, A. Fernandez, M. Ocana, A. Roig, E. Molins, K. O'Grady, and C. Serna, “Formation of γ-Fe2O3 Isolated Nanoparticles in a Silica Matrix,” Langmuir 13, no. 14 (1997): 3627–34. doi:https://doi.org/10.1021/la9700228.
- C. Pascal, J. Pascal, F. Favier, M. Elidrissi. Moubtassim, and C. Payen, “Electrochemical Synthesis for the Control of γ-Fe2O3 Nanoparticle Size. Morphology, Microstructure, and Magnetic Behavior,” Chemistry of Materials 11, no. 1 (1999): 141–7. doi:https://doi.org/10.1021/cm980742f
- Y. Zhang, Z. Li, W. Sun, and C. Xia, “A Magnetically Recyclable Heterogeneous Catalyst: cobalt Nano-Oxide Supported on Hydroxyapatite-Encapsulated γ-Fe2O3 Nanocrystallites for Highly Efficient Olefin Oxidation with H2O2,” Catalysis Communications 10, no. 2 (2008): 237–42. doi:https://doi.org/10.1016/j.catcom.2008.08.030
- A. Corma and H. García, “Lewis Acids: From Conventional Homogeneous to Green Homogeneous and Heterogeneous Catalysis,” Chemical Reviews 103, no. 11 (2003): 4307–66. doi:https://doi.org/10.1021/cr030680z
- V. Polshettiwar and R. S. Varma, “Green Chemistry by Nano-Catalysis,” Green Chemistry 12, no. 5 (2010): 743–54. doi:https://doi.org/10.1039/B921171C
- A. Maleki, “Fe3O4/SiO2 Nanoparticles: An Efficient and Magnetically Recoverable Nanocatalyst for the One-Pot Multicomponent Synthesis of Diazepines,” Tetrahedron 68, no. 38 (2012): 7827–33. doi:https://doi.org/10.1016/j.tet.2012.07.034
- M. Mamaghani, F. Shirini, M. Sheykhan, and M. Mohsenimehr, “Synthesis of a Copper(ii) Complex Covalently Anchoring a (2-Iminomethyl)Phenol Moiety Supported on HAp- Encapsulated-α-Fe2O3 as an Inorganic–Organic Hybrid Magnetic Nanocatalyst for the Synthesis of Primary and Secondary Amides,” RSC Advances 5, no. 55 (2015): 44524–9. doi:https://doi.org/10.1039/C5RA03977K
- M. Mohsenimehr, M. Mamaghani, F. Shirini, M. Sheykhan, S. Abbaspour, and L. S. Sabet, “One-Pot Synthesis of Novel Pyrimido[4,5-b]Quinolines and Pyrido[2,3-d: 6,5-d′]Dipyrimidines Using Encapsulated-γ-Fe2O3 Nanoparticles,” Journal of Chemical Sciences 127, no. 11 (2015): 1895–904. doi:https://doi.org/10.1007/s12039-015-0964-1
- M. Mohsenimehr, M. Mamaghani, F. Shirini, M. Sheykhan, and F. A. Moghaddam, “One-Pot Synthesis of Novel Pyrido[2,3-d]Pyrimidines Using HAp-Encapsulated-γ-Fe2O3 Supported Sulfonic Acid Nanocatalyst under Solvent-Free Conditions,” Chinese Chemical Letters 25, no. 10 (2014): 1387–91. doi:https://doi.org/10.1016/j.cclet.2014.04.025
- M. Mamaghani, M. Sheykhan, M. Sadeghpour, and F. Tavakoli, “An Expeditious One-Pot Synthesis of Novel Bioactive Indole-Substituted Pyrido[2,3-d]Pyrimidines Using Fe3O4@SiO2-Supported Ionic Liquid Nanocatalyst,” Monatshefte Für Chemie – Chemical Monthly 149, no. 8 (2018): 1437–46. doi:https://doi.org/10.1007/s00706-018-2166-2
- S. A. Mirfarjood, M. Mamaghani, and M. Sheykhan, “Copper-Incorporated Fluorapatite Encapsulated Iron Oxidenanocatalyst for Synthesis of Benzimidazoles,” Journal of Nanostructure in Chemistry 7, no. 4 (2017): 359–66. doi:https://doi.org/10.1007/s40097-017-0245-2
- Seyed-Abdollah Mirfarjood, Manouchehr Mamaghani, and Mehdi Sheykhan, “Copper-Exchanged magnetic-FAp: Surface Catalysis in Decarboxylative Coupling of α-Oxocarboxylic Acids with Formamides,” Chemistry Select 2, no. 27 (2017): 8650–7. doi:https://doi.org/10.1002/slct.201701438
- X. J. Qin, Y. L. Zhao, P. K. Lunga, X. W. Yang, C. W. Song, G. G. Cheng, L. Liu, Y. Y. Chen, Y. P. Liu, and X. D. Luo, “Indole Alkaloids with Antibacterial Activity from Aqueous Fraction of Alstonia scholaris,” Tetrahedron Letters. 71, no. 25 (2015): 4372–8. doi:https://doi.org/10.1016/j.tet.2015.04.046
- Mardia Telep El-Sayed, Sibel Suzen, Nurten Altanlar, Knut Ohlsen, and Andreas Hilgeroth, “Discovery of Bisindolyl-Substituted Cycloalkane-Anellated Indoles as Novel Class of Antibacterial Agents against S. aureus and MRSA,” Bioorganic & Medicinal Chemistry Letters 26, no. 1 (2016): 218–21. doi:https://doi.org/10.1016/j.bmcl.2015.10.085