참고문헌
- Basavaiah, D.; Rao, P. D.; Hyma, R. S. Tetrahedron 1996, 52, 8001 https://doi.org/10.1016/0040-4020(96)00154-8
- Ciganek, E. Organic Reactions; John Wiley & Sons: New York, 1997; Vol. 51, pp 201-350
- Drewes, S. E.; Roos, G. H. P. Tetrahedron 1988, 44, 4653 https://doi.org/10.1016/S0040-4020(01)86168-8
- Langer, P. Angew. Chem., Int. Ed. Engl. 2000, 39, 3049 https://doi.org/10.1002/1521-3773(20000901)39:17<3049::AID-ANIE3049>3.0.CO;2-5
- Kim, J. N.; Lee, K. Y. Curr. Org. Chem. 2002, 6, 627 https://doi.org/10.2174/1385272023374094
- Basavaiah, D.; Rao, A. J.; Satyanarayana, T. Chem. Rev. 2003, 103, 811 https://doi.org/10.1021/cr010043d
- Lee, C. G.; Lee, K. Y.; Kim, S. C.; Kim, J. N. Bull Korean Chem. Soc. 2005, 26, 485 https://doi.org/10.1007/s11814-009-0082-1
- Lee, C. G.; Gowrisankar, S.; Kim, J. N. Bull. Korean Chem. Soc. 2005, 26, 481 https://doi.org/10.5012/bkcs.2005.26.3.481
- Lee, M. J.; Lee, K. Y.; Kim, J. N. Bull. Korean Chem. Soc. 2005, 26, 477 https://doi.org/10.5012/bkcs.2005.26.3.477
- Gowrisankar, S.; Na, J. E.; Lee, M. J.; Kim, J. N. Bull. Korean Chem. Soc. 2005, 26, 319 https://doi.org/10.5012/bkcs.2005.26.2.319
- Lee, C. G.; Lee, K. Y.; Lee, S.; Kim, J. N. Tetrahedron 2005, 61, 1493 https://doi.org/10.1016/j.tet.2004.11.082
- Lee, K. Y.; Kim, T. H.; Kim, J. N. Bull. Korean Chem. Soc. 2004, 25, 1966 https://doi.org/10.5012/bkcs.2004.25.12.1966
- Gowrisankar, S.; Lee, C. G.; Kim, J. N. Tetrahedron Lett. 2004, 45, 6949 https://doi.org/10.1016/j.tetlet.2004.07.070
- Gowrisankar, S.; Lee, K. Y.; Lee, C. G.; Kim, J. N. Tetrahedron Lett. 2004, 45, 6141 https://doi.org/10.1016/j.tetlet.2004.06.057
- Lee, K. Y.; Gowrisankar, S.; Kim, J. N. Tetrahedron Lett. 2004, 45, 5485 https://doi.org/10.1016/j.tetlet.2004.05.064
- Kim, J. M.; Lee, K. Y.; Lee, S.-k.; Kim, J. N. Tetrahedron Lett. 2004, 45, 2805 https://doi.org/10.1016/j.tetlet.2004.02.047
- Lee, K. Y.; Kim, J. M.; Kim, J. N. Tetrahedron Lett. 2003, 44, 6737 https://doi.org/10.1016/S0040-4039(03)01648-4
- Kim, J. N.; Kim, J. M.; Lee, K. Y. Synlett 2003, 821
- Im, Y. J.; Lee, C. G.; Kim, H. R.; Kim, J. N. Tetrahedron Lett. 2003, 44, 2987 https://doi.org/10.1016/S0040-4039(03)00397-6
- Lee, K. Y.; Kim, J. M.; Kim, J. N. Synlett 2003, 357
- Lee, K. Y.; Kim, J. M.; Kim, J. N. Tetrahedron 2003, 59, 385
- Kim, J. N.; Lee, H. J.; Lee, K. Y.; Kim, H. S. Tetrahedron Lett. 2001, 42, 3737 https://doi.org/10.1016/S0040-4039(01)00552-4
- Kim, J. N.; Lee, K. Y.; Kim, H. S.; Kim, T. Y. Org. Lett. 2000, 2, 343 https://doi.org/10.1021/ol9903741
- Familoni, O. B.; Kaye, P. T.; Klaas, P. J. J. Chem. Soc., Chem. Commun. 1998, 2563
- Lee, K. Y.; Kim, J. N. Bull. Korean Chem. Soc. 2002, 23, 939 https://doi.org/10.5012/bkcs.2002.23.7.939
- Lee, K. Y.; Kim, J. M.; Kim, J. N. Bull. Korean Chem. Soc. 2002, 23, 1493 https://doi.org/10.5012/bkcs.2002.23.10.1493
- Kabalka, G. W.; Varma, R. S. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Oxford: Pergamon, 1991; Vol 8, pp 363-379
- Kamm, O. Org. Syn. Coll; 1932; Vol. 1, p 445
- Patrick, T. B.; Schield, J. A.; Kirchner, D. G. J. Org. Chem. 1974, 39, 1758 https://doi.org/10.1021/jo00925a037
- Ross, S. D.; Kahan, G. J.; Leach, W. A. J. Am. Chem. Soc. 1952, 74, 4122 https://doi.org/10.1021/ja01136a049
- Ross, S. D.; Kuntz, I. J. Am. Chem. Soc. 1952, 74, 1297 https://doi.org/10.1021/ja01125a046
- Kronja, O.; Matijevic-Sosa, J.; Ursic, S. J. Chem. Soc., Chem. Commun. 1987, 463
- Pilepic, V.; Ursic, S. Tetrahedron Lett. 1994, 35, 7425 https://doi.org/10.1016/0040-4039(94)85332-0
- Corbett, M. D.; Corbett, B. R. J. Org. Chem. 1980, 45, 2834 https://doi.org/10.1021/jo01302a017
- Ursic, S.; Pilepic, V.; Vrcek, V.; Gabricevic, M.; Zorc, B. J. Chem. Soc., Perkin Trans. 2 1993, 509
- Attanasi, O. A.; Filippone, P.; Fiorucci, C. Tetrahedron 1997, 53, 1467 https://doi.org/10.1016/S0040-4020(96)01081-2
- Boekelheide, V.; Linn, W. J. J. Am. Chem. Soc. 1954, 76, 1286 https://doi.org/10.1021/ja01634a026
- Coutts, R. T.; Wibberley, D. G. J. Chem. Soc. 1962, 2518
- Suzuki, M.; Ohuchi, Y.; Asanuma, H.; Kaneko, T.; Yokomori, S.; Ito, C.; Isobe, Y.; Muramatsu, M. Chem. Pharm. Bull. 2000, 48, 2003 https://doi.org/10.1248/cpb.48.2003
- Aoyagi, Y.; Abe, T.; Ohta, A. Synthesis 1997, 891
피인용 문헌
- Recent Advances in Construction of Nitrogen-containing Heterocycles from Baylis-Hillman Adducts vol.43, pp.1, 2011, https://doi.org/10.1080/00304948.2011.549065
- Synthesis of Quinoline N-Oxides from the Baylis—Hillman Adducts of 2-Nitrobenzaldehydes: Conjugate Addition of Nitroso Intermediate. vol.36, pp.48, 2005, https://doi.org/10.1002/chin.200548160
- The Baylis–Hillman approach to quinoline derivatives vol.4, pp.21, 2005, https://doi.org/10.1039/b608592j
- Synthesis of Indoles and Benzisoxazolines from Baylis-Hillman Adducts of 2-Nitrobenzaldehydes vol.28, pp.2, 2005, https://doi.org/10.5012/bkcs.2007.28.2.333
- Advances in the Baylis-Hillman reaction-assisted synthesis of cyclic frameworks vol.64, pp.20, 2008, https://doi.org/10.1016/j.tet.2008.02.087