References
- Basavaiah, D.; Pandiaraju, S. Tetrahedron Lett. 1995, 36, 757. https://doi.org/10.1016/0040-4039(94)02360-N
- Basavaiah, D.; Pandiaraju, S.; Krishnamacharyulu, M. Synlett 1996, 747.
- Shen, Y.; Zhang, Z. Synth. Commun. 2000, 30, 445. https://doi.org/10.1080/00397910008087341
- Shen, Y.; Zhang, Z. J. Chem. Res. (S) 1999, 556.
- Kim, J. N.; Lee, H. J.; Lee, K. Y.; Gong, J. H. Synlett 2002, 173.
- Gong, J. H.; Im, Y. J.; Lee, K. Y.; Kim, J. N. Tetrahedron Lett. 2002, 43, 1247. https://doi.org/10.1016/S0040-4039(01)02344-9
- Chung, Y. M.; Gong, J. H.; Kim, T. H.; Kim, J. N. Tetrahedron Lett. 2001, 42, 9023. https://doi.org/10.1016/S0040-4039(01)01972-4
- Kim, J. N.; Kim, H. S.; Gong, J. H.; Chung, Y. M. Tetrahedron Lett. 2001, 42, 8341. https://doi.org/10.1016/S0040-4039(01)01791-9
- Kim, J. N.; Im, Y. J.; Gong, J. H.; Lee, K. Y. Tetrahedron Lett. 2001, 42, 4195. https://doi.org/10.1016/S0040-4039(01)00687-6
- 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, H. S.; Kim, T. Y.; Lee, K. Y.; Chung, Y. M.; Lee, H. J.; Kim, J. N. Tetrahedron Lett. 2000, 41, 2613. https://doi.org/10.1016/S0040-4039(00)00229-X
- Kim, J. N.; Lee, K. Y.; Kim, H. S.; Kim, T. Y. Org. Lett. 2000, 2, 343. https://doi.org/10.1021/ol9903741
- Lee, H. J.; Seong, M. R.; Kim, J. N. Tetrahedron Lett. 1998, 39, 6223. https://doi.org/10.1016/S0040-4039(98)01280-5
- Lee, H. J.; Kim, H. S.; Kim, J. N. Tetrahedron Lett. 1999, 40, 4363. https://doi.org/10.1016/S0040-4039(99)00749-2
- Chung, Y. M.; Lee, H. J.; Hwang, S. S.; Kim, J. N. Bull. Korean Chem. Soc. 2001, 22, 799.
- Im, Y. J.; Kim, J. M.; Mun, J. H.; Kim, J. N. Bull. Korean Chem. Soc. 2001, 22, 349.
- Kim, J. N.; Lee, K. Y. Current Organic Chemistry 2002, 6, 627. https://doi.org/10.2174/1385272023374094
- Taber, D. F.; Amedio, J. C., Jr.; Gulino, F. J. Org. Chem. 1989, 54, 3474. https://doi.org/10.1021/jo00275a038
- Taber, D. F.; Amedio, J. C., Jr.; Patel, Y. K. J. Org. Chem. 1985, 50, 3618. https://doi.org/10.1021/jo00219a035
- Miles, D. H.; Huang, B.-S. J. Org. Chem. 1976, 41, 208. https://doi.org/10.1021/jo00864a006
- Huang, B.-S.; Parish, E. J.; Miles, D. H. J. Org. Chem. 1974, 39, 2647. https://doi.org/10.1021/jo00931a051
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