References
- Greene, T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis; Wiley: New York, 1999; pp 494-564
- Mulzer, J. In Comprehensive Organic Synthesis, Trost, B. M.; Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 6, pp 322-417
- Vogel, A. Practical Organic Chemistry, Longman Scientific & Technical and Wiley: New York, 1989; pp 708-710
- Smith, M. B.; March, J. March's Advanced Organic Chemistry, 5th ed.; Wiley: New York, 2001; pp 506-512
- Kang, Y. J.; Chung, H. A.; Kim, J. J.; Yoon, Y. J. Synthesis 2002, 733
- Wakasugi, K.; Nakamura, A.; Tanabe, Y. Tetrahedron Lett. 2001, 42, 7427 https://doi.org/10.1016/S0040-4039(01)01444-7
- Katrizky, A. R.; He, H.-Y.; Suzuki, K. J. Org. Chem. 2000, 65, 8210 https://doi.org/10.1021/jo000792f
- Kondo, K.; Sekimoto, E.; Nakao, J.; Murakami, Y. Tetrahedron 2000, 56, 5843 https://doi.org/10.1016/S0040-4020(00)00549-4
- Yasuhara, T.; Nagaoka, Y.; Tomioka, K. J. Chem. Soc., Perkin Trans. 1 1999, 2233
- Blagbrough, I. S.; Geall, A. J. Tetrahedron Lett. 1998, 39, 439 https://doi.org/10.1016/S0040-4039(97)10542-1
- Kartrizky, A. R.; Yang, B.; Semenzin, D. J. Org. Chem. 1997, 62, 726 https://doi.org/10.1021/jo961537r
- Kartrizky, A. R.; Chang, H. X. Synthesis 1995, 503
- Murahashi, S.-I.; Naota, T. Synthesis 1993, 433
- Akikusa, N.; Mitsui, K.; Sakamoto, T.; Kikugawa, Y. Synthesis 1992, 1058
- Kikukawa, Y.; Mitsui, K.; Sakamoto, T.; Kawase, M.; Tamiya, H. Tetrahedorn Lett. 1990, 31, 243 https://doi.org/10.1016/S0040-4039(00)94382-X
- Murahashi, S.-I.; Naota, T.; Nakajima, N. Chem. Lett. 1987, 879
- Murahashi, S.-I.; Naota, T.; Saito, E. J. Am. Chem. Soc. 1986, 108, 7846 https://doi.org/10.1021/ja00284a066
- Atwell, G. L.; Denny, W. A. Synthesis 1984, 1032
- Staab, H. A.; Walther, G. Angew. Chem. 1960, 72, 35
- Kim, J. J.; Park, Y. D.; Lee, W. S.; Cho, S. D.; Yoon, Y. J. Synthesis 2003, 1517
- Kim, J. J.; Park, Y. D.; Kweon, D. H.; Kang, Y. J.; Kim, H. K.; Lee, S. G.; Cho, S. D.; Lee, W. S.; Yoon, Y. J. Bull. Kor. Chem. 2004, 25, 501 https://doi.org/10.5012/bkcs.2004.25.4.501
- Lee, S. G.; Kim, J. J.; Kim, H. K.; Kweon, D. H.; Kang, Y. J.; Cho, S. D.; Kim, S. K.; Yoon, Y. J. Curr. Org. Chem. 2004, 8, 1463 https://doi.org/10.2174/1385272043369818
- Won, J. E.; Kim, H. K.; Kim, J. J.; Yim, H. S.; Kim, M. J.; Kang, S. B.; Chung, H. A; Lee, S. G.; Yoon, Y. J. Tetrahedron 2007, 63, 12720 https://doi.org/10.1016/j.tet.2007.10.011
- Chung, H. A.; Kweon, D. H.; Kang, Y. J.; Park, J. W.; Yoon, Y. J. J. Heterocylic Chem. 1999, 36, 905 https://doi.org/10.1002/jhet.5570360413
- Cho, S. D.; Choi, W. Y.; Yoon, Y. J. J. Heterocyclic Chem. 1996, 33, 1579 https://doi.org/10.1002/jhet.5570330605
- Zacuto, M. J.; Xu, F. J. Org. Chem. 2007, 72(16), 6298 https://doi.org/10.1021/jo070553t
- Liley, M. J.; Johnson, T.; Gibson, S. E. J. Org. Chem. 2006, 71(4), 1322 https://doi.org/10.1021/jo051742j
- Fairfull-Smith, K. E.; Jenkins, I. D.; Loughlin, W. A. Org. & Biomol. Chem. 2004, 2(14), 1979 https://doi.org/10.1039/b406770c
- Wang, X.; Widenhoefer, R. A. Organometallics 2004, 23(8), 1649 https://doi.org/10.1021/om0498549
- Shaabani, A.; Soleimani, E.; Rezayan, A. H. Tetrahedron Lett. 2007, 48(35), 6137 https://doi.org/10.1016/j.tetlet.2007.06.136
- Wu, X.; Ekegren, J. K.; Larhed, M. Orgnometallics 2006, 25(6), 1434 https://doi.org/10.1021/om051044p
- Gertzmann, R.; Guertler, C. Tetrahedron Lett. 2005, 46(39), 6659 https://doi.org/10.1016/j.tetlet.2005.07.156
- Khan, M. W.; Reza, A. F. G. M. Tetrahedron 2005, 61(47), 11204 https://doi.org/10.1016/j.tet.2005.09.032
- Ruan, Z.; Lawrence, R. M.; Cooper, C. B. Tetrahedron Lett. 2006, 47(43), 7649 https://doi.org/10.1016/j.tetlet.2006.08.024
- Bandgar, S. B.; Bandgar, B. P.; Korbad, B. L.; Sawant, S. S. Tetrahedron Lett. 2007, 48(7), 1287 https://doi.org/10.1016/j.tetlet.2006.12.024
- Kumar, A.; Narasimhan, B.; Kumar, D. Bioorg. & Med. Chem. 2007, 15(12), 4113 https://doi.org/10.1016/j.bmc.2007.03.074
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