참고문헌
- Faust, R. Angew. Chem., Int. Ed. 2001, 40, 2251 https://doi.org/10.1002/1521-3773(20010618)40:12<2251::AID-ANIE2251>3.0.CO;2-R
- Salaun, J. Top. Curr. Chem. 2000, 207, 1 https://doi.org/10.1007/3-540-48255-5_1
- Djerassi, C.; Doss, G. A. New. J. Chem. 1990, 14, 713
- Srikrishna, A.; Krishnan, K. Tetrahedron 1992, 48, 3429 https://doi.org/10.1016/0040-4020(92)85016-8
- Yadav, J. S.; Mysorekar, S. V.; Rao, A. V. R. Tetrahedron 1989, 45, 7353 https://doi.org/10.1016/S0040-4020(01)89196-1
- Leeper, F. J.; Padmanabhan, P.; Kirby, G. W.; Sheldrake, G. N. J. Chem. Soc., Chem. Commun. 1987, 505
- Piers, E. In Comprehensive Organic Synthesis; Trost, B. M., Ed.; Pergamon Press: Oxford, 1991; Vol. 5, p 971
- Nonhebel, D. C. Chem. Soc. Rev. 1993, 347
- Reissig, H.-U. Top. Curr. Chem. 1988, 144, 73 https://doi.org/10.1007/BFb0111229
- Wong, H. N. C.; Hon, M.-Y.; Tse, C.-W.; Yip, Y.-C.; Tanko, J.; Hudlicky, T. Chem. Rev. 1989, 89, 165 https://doi.org/10.1021/cr00091a005
- Goldschmidt, Z.; Crammer, B. Chem. Soc. Rev. 1988, 17, 229 https://doi.org/10.1039/cs9881700229
- Hudlicky, T.; Fan, R.; Reed, J.; Gadamasetti, K. G. Org. React. 1992, 41, 1
- Davies, H. M. L. Tetrahedron 1993, 49, 5203 https://doi.org/10.1016/S0040-4020(01)82371-1
- Mann, J. Tetrahedron 1986, 42, 4611 https://doi.org/10.1016/S0040-4020(01)82046-9
- Doyle, M. P. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH: Weinheim, 1993; p 63
- Salaun, J. Chem. Rev. 1989, 89, 1247 https://doi.org/10.1021/cr00095a017
- Lautens, M.; Klute, W.; Tam, W. Chem. Rev. 1996, 96, 49 https://doi.org/10.1021/cr950016l
- Charette, A. B.; Marcoux, J.-F. Synlett 1995, 1197
- Reissig, H.-U. Angew. Chem., Int. Ed. 1996, 35, 971 https://doi.org/10.1002/anie.199609711
- Aratani, T. Pure Appl. Chem. 1985, 57, 1839 https://doi.org/10.1351/pac198557121839
- Hartley, R. C.; Caldwell, S. T. J. Chem. Soc., Perkin Trans. 1 2000, 477
- Donalson, W. A. Tetrahedron 2001, 57, 8589 https://doi.org/10.1016/S0040-4020(01)00777-3
- Simmons, H. E.; Cairns, T. L.; Vladuchick, S. A.; Hoiness, C. M. Org. React. 1973, 20, 1
- Furukawa, J.; Kawabata, N. Adv. Organomet. Chem. 1974, 12, 83 https://doi.org/10.1016/S0065-3055(08)60451-7
- Boersma, J. In Comprehensive Organometallic Chemistry; Wilkinson, G., Ed.; Pergamon Press: New York, 1984; Vol. 2. Chapter 16
- Charette, A. B.; Beauchemin, A. Org. React. 2001, 58, 1
- Denmark, S. E.; Beutner, G. In Cycloaddition Reactions in Organic Synthesis; Kobayashi, S., Jorgensen, K. A., Eds.; Wiley-VCH: New York, 2001; p 85
- Fang, W.-H.; Phillips, D. L.; Wang, D.-Q.; Li, Y.-L. J. Org. Chem. 2002, 67, 154 https://doi.org/10.1021/jo0107655
- Doyle, M. P.; Forbes, D. C. Chem. Rev. 1998, 98, 911 https://doi.org/10.1021/cr940066a
- Rovis, T.; Evans, D. A. Prog. Inorg. Chem. 2001, 57, 1
- Singh, V. K.; DattaGupta, A.; Sekar, G. Synthesis 1997, 137
- Calter, M. A. Curr. Org. Chem. 1997, 1, 37
- Evans, D. A.; Woerpel, K. A.; Hinman, M. M.; Faul, M. M. J. Am. Chem. Soc. 1991, 113, 726 https://doi.org/10.1021/ja00002a080
- Evans, D. A.; Woerpel, K. A.; Scott, M. J. Angew. Chem. Int. Ed. 1992, 31, 430 https://doi.org/10.1002/anie.199204301
- Tang, W.; Hu, X.; Zhang, X. Tetrahedron Lett. 2002, 43, 3075 https://doi.org/10.1016/S0040-4039(02)00317-9
- Escribano, A.; Pedregal, C.; González, R.; Fernández, A.; Burton, K.; Stephenson, G. A. Tetrahedron 2001, 57, 9423 https://doi.org/10.1016/S0040-4020(01)00949-8
- Calo, V.; Nacci, A.; Lopez, L.; Lerario, V. L. Tetrahedron Lett. 2000, 41, 8977 https://doi.org/10.1016/S0040-4039(00)01593-8
- Artaud, I.; Seyden-Penne, J.; Viout, P. Synthesis 1980, 34
- Hudlicky, T.; Radesca, L.; Luna, H.; Anderson, F. E. J. Org. Chem. 1986, 51, 4746 https://doi.org/10.1021/jo00374a055
- Hakam, K.; Thielmann, M.; Thielmann, T.; Winterfeldt, E. Tetrahedron 1987, 43, 2035 https://doi.org/10.1016/S0040-4020(01)86785-5
- Badiani, K.; Lightfoot, P.; Gani, D. J. Chem. Soc., Chem. Commun. 1996, 675
- Cluet, F.; Haudrechy, A.; Leber, P.; Sinay, P.; Wick, A. Synlett 1994, 913
- Shibata, I.; Mori, Y.; Yamasaki, H.; Bada, A.; Matsuda, H. Tetrahedron Lett. 1993, 34, 6567 https://doi.org/10.1016/0040-4039(93)88106-S
- Lee, Y. R.; Hwang, J. C. Eur. J. Org. Chem. 2005, 1568
- Lee, Y. R.; Cho, B. S.; Kwon, H. J. Tetrahedron 2003, 59, 9333 https://doi.org/10.1016/j.tet.2003.09.087
- Lee, Y. R.; Kim, D. H. Tetrahedron Lett. 2001, 42, 6561 https://doi.org/10.1016/S0040-4039(01)01345-4
- Lee, Y. R.; Suk, J. Y.; Kim, B. S. Tetrahedron Lett. 1999, 40, 8219 https://doi.org/10.1016/S0040-4039(99)01714-1
- Lee, Y. R.; Suk, J. Y. Chem. Commun. 1998, 2621
- Lee, Y. R.; Suk, J. Y. Tetrahedron 2002, 58, 2359 https://doi.org/10.1016/S0040-4020(02)00118-7
- Lee, Y. R.; Suk, J. Y. Tetrahedron Lett. 2000, 41, 4795 https://doi.org/10.1016/S0040-4039(00)00716-4
- Lee, Y. R.; Suk, J. Y.; Kim, B. S. Tetrahedron Lett. 1999, 40, 6603 https://doi.org/10.1016/S0040-4039(99)01317-9
- Taber, D. F.; Ruckle Jr., R. E.; Hennessy, M. J. J. Org. Chem. 1986, 51, 4077 https://doi.org/10.1021/jo00371a034
- Ostergaard, N.; Jensen, J. F.; Tanner, D. Tetrahedron 2001, 57, 6083 https://doi.org/10.1016/S0040-4020(01)00583-X
- Davies, H. M. L.; Beckwith, R. E. J. Chem. Rev. 2003, 103, 2861 https://doi.org/10.1021/cr0200217
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