References
- Zakharkin, L. I.; Khorlina, I. M. Terahedron Lett. 1962, 619
- Kim, S. H.; Kim, J. H.; Yoon, N. M. Bull. Korean Chem. Soc. 1989, 10, 117
- Weissman, P. M.; Brown, H. C. J. Org. Chem. 1966, 31, 283 https://doi.org/10.1021/jo01339a063
- Muraki, M.; Mukaiyama, T. Chem. Lett. 1975, 215
- Cha, J. S.; Kwon, S. S. J. Org. Chem. 1987, 55, 5486
- Yoon, N. M.; Ahn, J. H.; An, D. K.; Shon, Y. S. J. Org. Chem. 1993, 58, 1941 https://doi.org/10.1021/jo00059a058
- Yoon, N. M.; Shon, Y. S.; Ahn, J. H.; An, J. W. Bull. Korean Chem. Soc. 1993, 14, 522
- Kim, S.; Ahn, K. H. J. Org. Chem. 1984, 49, 1717 https://doi.org/10.1021/jo00184a010
- Cha, J. S.; Kwon, S. Y.; Kim, J. M.; Kwon, O. O.; Lee, K. W. Bull. Korean Chem. Soc. 1999, 20, 737
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