참고문헌
- Joseph, T.; Kumar, K. V.; Ramaswamy, A. V.; Halligudi, S. B. Catal. Commun. 2007, 8, 629. https://doi.org/10.1016/j.catcom.2006.03.004
- Khan, F. A.; Dash, J.; Sudheer, C.; Gupta, R. K. Tetrahedron Lett. 2003, 44, 7783. https://doi.org/10.1016/j.tetlet.2003.08.080
- Rai, G.; Jeong, J. M.; Lee, Y. S.; Kim, H. W.; Lee, D. S.; Chung, J. K.; Leea, M. C. Tetrahedron Lett. 2005, 46, 3987. https://doi.org/10.1016/j.tetlet.2005.04.035
- Figueras, F.; Coq, B. J. Mol. Catal. A: Chem. 2001, 173, 223. https://doi.org/10.1016/S1381-1169(01)00151-0
- Tan, X. Y.; Zhang, Z. X.; Xiao, Z. H.; Xu, Q.; Liang, C. H.; Wang, X. H. Catal. Lett. 2012, 142, 788. https://doi.org/10.1007/s10562-012-0821-5
- Zheng, Y. F.; Ma, K.; Wang, H. L.; Sun, X.; Jiang, J.; Wang, C. F.; Li, R.; Ma, J. T. Catal. Lett. 2008, 124, 268. https://doi.org/10.1007/s10562-008-9452-2
- Lagrost, C.; Preda, L.; Volanschi, E.; Hapiot, P. J. Electroanal. Chem. 2005, 585, 1. https://doi.org/10.1016/j.jelechem.2005.06.013
- Magdalene, R. M.; Leelamani, E. G.; Nanje, G. N. M. J. Mol.Catal A: Chem. 2004, 223, 17. https://doi.org/10.1016/j.molcata.2003.12.041
- Cardenas-Lizana, F.; Gomez-Quero, S.; Keane, M. A. Catal. Commun. 2008, 9, 475. https://doi.org/10.1016/j.catcom.2007.07.032
- Vilella, I. M. J.; Miguel, S. R.; Scelza, O. A. Chem. Eng. J. 2005, 114, 33. https://doi.org/10.1016/j.cej.2005.08.011
- Kuroda, K.; Ishida, T.; Haruta, M. J. Mol. Catal A: Chem. 2009, 298, 7. https://doi.org/10.1016/j.molcata.2008.09.009
- Swathi, T.; Buvaneswari, G. Materials Lett. 2008, 62, 3900. https://doi.org/10.1016/j.matlet.2008.05.028
- Kumar, P. S.; Rai, K. L. Chemical Papers 2012, 66, 772. https://doi.org/10.2478/s11696-012-0195-6
- Gowda, S.; Gowda, D. C. Tetrahedron. 2002, 58, 2211. https://doi.org/10.1016/S0040-4020(02)00093-5
- Ley, S. V.; Thomas, A. W. Angew. Chem. Int. Ed. 2003, 42, 5400. https://doi.org/10.1002/anie.200300594
- Reymond, S.; Cossy, J. Chem. Rev. 2008, 108, 5359. https://doi.org/10.1021/cr078346g
- Qiu, G. M.; Wang, C. J.; Zhang, Y. J.; Huang, S.; Liu, X. L.; Zhang, B. J.; Zhou, X. L. Bull. Korean Chem. Soc. 2012, 33, 2603. https://doi.org/10.5012/bkcs.2012.33.8.2603
- Lu, L.; Sui, M. L.; Lu, K. Science 2000, 287, 1463. https://doi.org/10.1126/science.287.5457.1463
- Safaei-Ghomi, J.; Ziarati, A.; Teymuri, R. Bull. Korean Chem. Soc. 2012, 33, 2679. https://doi.org/10.5012/bkcs.2012.33.8.2679
- Ranjit, S.; Duan, Z.; Zhang, P.; Liu, X. Org. Lett. 2010, 12, 4134. https://doi.org/10.1021/ol101729k
- Khan, F. A.; Dash, J.; Sudheer, C.; Gupta, R. K. Tetrahedron Lett. 2003, 44, 7783. https://doi.org/10.1016/j.tetlet.2003.08.080
- Chaubal, N. S.; Sawant, M. R. J. Mol. Catal A: Chem. 2007, 261, 232. https://doi.org/10.1016/j.molcata.2006.06.033
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