참고문헌
- Lee, J. H.; Bang, H. B.; Han, S. Y.; Jun, J. G. Tetrahedron Lett. 2007, 48, 2889. https://doi.org/10.1016/j.tetlet.2007.02.088
- Manian, R. D. R. S.; Jayashankaran, J.; Raghunathan, R. A. Tetrahedron Lett. 2007, 48, 1385. https://doi.org/10.1016/j.tetlet.2006.12.106
- Zhao, H.; Neamati, N.; Hong, H.; Mazumder, A.; Wang, S.; Sunder, S.; Milne, G. W. A.; Pommier, Y.; Burke, T. R. J. Med. Chem. 1997, 40, 242. https://doi.org/10.1021/jm960450v
- Appendino, G.; Cravotto, G.; Tagliapietra, S.; Ferraro, S.; Nano, G. M.; Palmisano, G. Helv. Chim. Acta. 1991, 74, 1451. https://doi.org/10.1002/hlca.19910740708
- Manolov. I.; Moessmer, C. M.; Danchev, N. D. Eur. J. Med. Chem. 2006, 41, 882. https://doi.org/10.1016/j.ejmech.2006.03.007
- Khan, K. M.; Iqbal, S.; Lodhi, M. A.; Maharvi, G. M.; Zia-u-Allah Choudhary, M. I.; Rahman, A. U.; Perveen, S. Bioorg. Med. Chem. 2004, 12, 1963. https://doi.org/10.1016/j.bmc.2004.01.010
- Wang, J.; Shi, D. Q.; Zhuang, Q. Y.; Wang, X. S.; Tu, S. J. Chin. J. Org. Chem. 2005, 25, 926.
- Kidwi, M.; Bansal, V.; Mothsra, P.; Saxena, S.; Somvanshi, R. K.; Dey, S.; Singh, T. P. J. Mol. Catal. A:Chem. 2007, 268, 76. https://doi.org/10.1016/j.molcata.2006.11.054
- Khurana, J. M.; Kumar, S. Tetrahedron Lett. 2009, 50, 4125. https://doi.org/10.1016/j.tetlet.2009.04.125
- Qadir, S.; Ahmad Dar, A.; Zaman Khan, Kh. Syn. Commun. 2008, 38, 3490. https://doi.org/10.1080/00397910802162942
- Gong, G. X.; Zhou, J. F.; An, L. T.; Duan, X. L.; Ji, S. J. Syn. Commun. 2009, 39, 497. https://doi.org/10.1080/00397910802398272
- Pope, M. T. Heteropoly and Isopoly Oxometalates; Springer-Verlag: Berlin, 1983.
- Mizuno, N.; Misono, M. Chem. Rev. 1998, 98, 199. https://doi.org/10.1021/cr960401q
- Sadakane, M.; Steckhan, E. Chem. Rev. 1998, 98, 219. https://doi.org/10.1021/cr960403a
- Coronado, E.; Gomez-Garcia, C. J. Chem. Rev. 1998, 98, 273. https://doi.org/10.1021/cr970471c
- Katsoulis, D. E. Chem. Rev. 1998, 98, 359. https://doi.org/10.1021/cr960398a
- Kozhevnikov, I. V. In Catalysts for Fine Chemical Synthesis, Catalysis by Polyoxometalates 2, Derouane, E., Ed.; Wiley: New York, 2002.
- Okuhara, T.; Mizuno, N.; Misono, M. Adv. Catal. 1996, 41, 113. https://doi.org/10.1016/S0360-0564(08)60041-3
- Pope, M. T. In Progress in Inorganic Chemistry; Lippard, S. J., Ed.; Wiley: New York, 1991, 39, 181. https://doi.org/10.1002/9780470166406.ch4
- Hill, C. L. J. Mol. Catal. A: Chem. 1996, 114, 1. https://doi.org/10.1016/S1381-1169(96)00338-X
- Hill, C. L. Chem. Rev. 1998, 98, 1. https://doi.org/10.1021/cr960395y
- Gouzerh, P.; Proust, A. Chem. Rev. 1998, 98, 77. https://doi.org/10.1021/cr960393d
- Strong, J. B.; Yap, G. P. A.; Ostrander, R.; Liable-Sands, L. M.; Rheingold, A. L.; Thouvenot, R.; Gouzerh, P.; Maatta E. A. J. Am. Chem. Chem. 2000, 122, 639. https://doi.org/10.1021/ja9927974
- Davoodnia, A.; Allameh, S.; Fakhari, A. R.; Tavakoli-Hoseini, N. Chin. Chem. Lett. 2010, 21, 550. https://doi.org/10.1016/j.cclet.2010.01.032
- Zeinali-Dastmalbaf, M.; Davoodnia, A.; Heravi, M. M.; Tavakoli- Hoseini, N.; Khojastehnezhad, A.; Zamani, H. A. Bull. Korean Chem. Soc. 2011, 32, 656. https://doi.org/10.5012/bkcs.2011.32.2.656
- Davoodnia, A.; Tavakoli-Nishaburi, A.; Tavakoli-Hoseini, N. Bull. Korean Chem. Soc. 2011, 32, 635. https://doi.org/10.5012/bkcs.2011.32.2.635
- Davoodnia, A.; Khojastehnezhad, A.; Tavakoli-Hoseini, N. Bull. Korean Chem. Soc. 2011, 32, 2243. https://doi.org/10.5012/bkcs.2011.32.7.2243
- Fournier, M. In Inorganic Synthesis; Ginsberg, A. P., Ed.; John Wiley: New York, 1990, 27, 80.
- Chary, M. V.; Keerthysri, N. C.; Vupallapati, S. V. N.; Lingaiah, N.; Kantevari, S. Catal. Commun. 2008, 9, 2013. https://doi.org/10.1016/j.catcom.2008.03.037
- Reinheimer, E. W.; Fourmigue, M.; Dunbar, K. R. J. Chem. Crystallogr. 2009, 39, 723. https://doi.org/10.1007/s10870-009-9521-4
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