[1]
|
A. U. Lesanko and D. G. Hall, “Wanted: New Multicomponent Reactions for Generating Libraries of Polycyclic Natural Products,” Current Opinion in Chemical Biology, Vol. 9, No. 3, 2005, pp. 266-276.
doi:10.1016/j.cbpa.2005.04.003
|
[2]
|
N. Li, P. Wang, S. L. Lai, W. Liu, C. S. Lee, S. T. Lee and Z. Liu, “Synthesis of Multiaryl-Substituted Pyridine Derivatives and Applications in Non-Doped Deep-Blue OLEDs as Electron-Transporting Layer with High Hole-Blocking Ability,” Advanced Materials, Vol. 22, No. 4, 2010, pp. 527-530. doi:10.1002/adma.200902430
|
[3]
|
L. C. W. Chang, J. K. Von Frijtag, D. Kunzel, T. M. Mulder-Kriegger, R. F. Spangersberg, S. F. Roerink, G. Hout, M. W. Beukers, J. Brussee and A. P. Ijzerman, “A Series of Ligands Displaying a Remarkable Agonistic-Antagonistic Profile at the Adenosine A1 Receptor,” Journal of Medicinal Chemistry, Vol. 48, No. 6, 2005, pp. 2045-2053. doi:10.1021/jm049597+
|
[4]
|
M. W. Beukers, L. W. Chang, J. K. von Frijtag, D. Künzel, T. Mulder-Krieger, R. F. Spanjersberg, J. Brussee and A. P. I. Jzerman, “New, Non-Adenosine, High-Potency Agonists for the Human Adenosine A2B Receptor with an Improved Selectivity Profile Compared to the Reference Agonist N-Ethylcarboxamidoadenosine,” Journal of Medicinal Chemistry, Vol. 47, No. 15, 2004, pp. 3707-3709.
doi:10.1021/jm049947s
|
[5]
|
A. D. Pillai, P. D. Rathod, P. X. F. M. Patel, M. Nivsarkar, K. K. Vasu, H. Padh and V. Sudarsanam, “Novel Drug Designing Approach for Dual Inhibitors as Anti-Inflammatory Agents: Implication of Pyridine Template,” Biochemical and Biophys Research Communications, Vol. 301, No. 1, 2003, pp. 183-186.
doi:10.1016/S0006-291X(02)02996-0
|
[6]
|
G. W. Cave, M. J. Hardie, B. A. Roberts and C. L. Raston, “A Versatile Six-Component Molecular Capsule Based on Benign Synthons—Selective Confinement of a Heterogeneous Molecular Aggregate,” European Journal of Organic Chemistry, Vol. 2001, No. 17, 2001, pp. 3227-3231. doi:10.1002/1099-0690(200109)2001:17<3227::AID-EJOC3227>3.0.CO;2-V
|
[7]
|
R. R. Jetti, A. Nagia, F. Xue and T. C. W. Mak, “Polar Host-Guest Assembly Mediated by Halogen…π Interaction: Inclusion Complexes of 2,4,6-Tris (4-halophenoxy)-1,3,5-triazine (Halo = Chloro, Bromo) with Trihalobenzene (Halo = Bromo, Iodo),” Chemical Communications, No. 10, 2001, pp. 919-920. doi:10.1039/b102150h
|
[8]
|
Z. C. Watson, N. Bampos and J. M. Sanders, “Mixed Cyclic Trimers of Porphyrins and Dioxoporphyrins: Geometry vs. Electronics in Ligand Recognition,” New Journal of Chemistry, Vol. 22, No. 11, 1998, pp. 1135-1138.
doi:10.1039/a805504a
|
[9]
|
F. Chubb, A. S. Hay and R. B. Sandin, “The Leuckart Reaction of Some 1,5-Diketones,” Journal of American Chemical Society, Vol. 75, No. 23, 1953, pp. 6042-6044.
doi:10.1021/ja01119a508
|
[10]
|
R. S. Tewari and A. K. Dubey, “Studies on Cycloimmonium Ylides. Synthesis of Some 2,4,6-Triaryl-Substituted Pyridines via Isoquniolinium Ylides,” Journal of Chemical Engineering Data, Vol. 25, No. 1, 1980, pp. 91-92.
doi:10.1021/je60084a032
|
[11]
|
S. P. Kendurkar and R. S. Tewari, “Synthesis of Some New 2,4,6-Triaryl-Substituted Pyridines Via Aroylmethy-lenepyridinium Ylides,” Journal of Chemical Engineering Data, Vol. 19, No. 2, 1974, pp. 184-188.
doi:10.1021/je60061a004
|
[12]
|
F. Krohnke, W. Zecher, J. Curtze, D. Drechsler, K. Pfleghar, K. E. Schnalke and W. Weis, “Syntheses Using the Michael Adddition of Pyridinium Salts,” Angewandte Chemie International Edition in English, Vol. 1, No. 12, 1962, pp. 626-632. doi:10.1002/anie.196206261
|
[13]
|
K. T. Potts, M. J. Cipullo, P. Ralli and G. Theodoridis, “Ketenedithioacetals as Synthetic Intermediates. A Versatile Synthesis of Pyridenes, Polypyridinyls, and Pyrylium Salts,” Journal of American Chemical Society, Vol. 103, No. 12, 1981, pp. 3584-3585.
http://dx.doi.org/10.1021/ja00402a062
|
[14]
|
T. Kobayashi, H. Kakiuchi and H. Kato, “On the Reaction of N-(Diphenylphosphinyl)-1-phenylethanimine with Aromatic Aldehydes Giving 4-Aryl-2,6-diphenylpyridine Derivatives,” Bulletin of the Chemical Society of Japan, Vol. 64, No. 2, 1991, pp. 392-395. doi:10.1246/bcsj.64.392
|
[15]
|
F. Palacios, A. O. Retana and J. A. Oyarzabal, “A ‘One Pot’ Synthesis of Polysubstituted Pyridines from Metallated Alkylphosphonates, Nitriles and α,β-Unsaturated Ketones,” Tetrahedron Letters, Vol. 37, No. 26, 1996, pp. 4577-4580. doi:10.1016/0040-4039(96)00850-7
|
[16]
|
G. W. V. Cave and C. L. Raston, “Towards Benign SynThesis of Pyridines Involving Sequential Solvent Free Aldol and Michael Addition Reactions,” Chemical Communications, No. 22, 2000, pp. 2199-2200.
doi:10.1039/b007431o
|
[17]
|
S. Tu, T. Li, F. Shi, F. Fang, S. Zhu, X. Wei and Z. Zong, “An Efficient Improve for the Krohnke Reaction: One-Pot Synthesis of 2,4,6-Triarylpyridines Using Raw Materials under Microwave Irradiation,” Chemistry Letters, Vol. 34, No. 5, 2005, pp. 732-733.
doi:10.1246/cl.2005.732
|
[18]
|
K. Motokura, S. Matsunaga, A. Miyaji, Y. Sakamoto and T. Baba, “Heterogeneous Allylsilation of Aromatic and Aliphatic Alkenes Catalyzed by Proton-Exchanged Montmorillonite,” Organic Letters, Vol. 12, No. 7, 2010, pp. 1508-1511. doi:10.1021/ol100228t
|
[19]
|
K. Motokura, M. Tada and Y. Iwasawa, “Layered Materials with Coexisting Acidic and Basic Sites for Catalytic One-Pot Reaction Sequences,” Journal of American Chemical Society, Vol. 131, No. 23, 2009, pp. 7944-7945.
doi:10.1021/ja9012003
|
[20]
|
M. Nose, T. Mizugaki, K. Jitsukawa and K. Kaneda, “Reusable Montmorillonite-Entrapped Organocatalyst for Asymmetric Diels-Alder Reaction,” Tetrahedron Letters, Vol. 49, No. 38, 2008, pp. 5464-5466.
doi:10.1016/j.tetlet.2008.07.011
|
[21]
|
S. B. Neji, M. Trabelsi and M. H. Frikha, “Esterification of Fatty Acids with Short-Chain Alcohols over Commercial Acid Clays in a Semi-Continuous Reactor,” Energies, Vol. 2, No. 4, 2009, pp. 1107-1117.
doi:10.3390/en20401107
|
[22]
|
M. R. Dintzner, Y. A. Mondjnou and D. J. Pileggi, “Montmorillonite Clay-Catalyzed Cyclotrimerization and Oxidation of Aliphatic Aldehydes,” Tetrahedron Letters, Vol. 51, No. 5, 2010, pp. 826-827.
doi:10.1016/j.tetlet.2009.12.009
|
[23]
|
T. Kobayashi, H. Kakiuchi and H. Kato, “On the Reaction of N-(Diphenylphosphinyl)-1-phenylethanimine with Aromatic Aldehydes Giving 4-Aryl-2,6-diphenylpyridine Derivatives,” Bulletin of the Chemical Society of Japan, Vol. 64, No. 2, 1991, pp. 392-395. doi:10.1246/bcsj.64.392
|
[24]
|
P. G. Ingole, S. V. Jadhav and H. C. Bajaj, “Ionic Liquid Mediated One Pot Synthesis of Substituted 2,4,6-Triarylpyridines,” International Journal of Chemical Technological Research, Vol. 2, No. 1, 2010, pp. 289-294.
|
[25]
|
M. Adib, H. Tahermansouri, S. A. Koloogani, B. Mohammadi and H. R. Bijanzadeh, “Krohnke Pyridines: An Efficient Solvent Free Synthesis of 2,4,6-triarylpyridines,” Tetrahedron Letters, Vol. 47, No. 33, 2006, pp. 5957- 5960. doi:10.1016/j.tetlet.2006.01.162
|
[26]
|
X. Q. Huang, H. X. Li, J. X. Wang and X. F. Jia, “A Rapid and Efficient Synthesis of 2,4,6-Triarylpyridines under Microwave Irradiation,” Chinese Chemical Letters, Vol. 16, No. 5, 2005, pp. 607-608.
|