References
- Green, T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis, 3rd ed.; Wiley-Interscience: New York, 1999.
- Sheehan, J. C.; Yang, D. D. H. J. Am. Chem. Soc. 1958, 80, 1154. https://doi.org/10.1021/ja01538a036
- Waki, J.; Meienhofer, J. J. Org. Chem. 1977, 42, 2019. https://doi.org/10.1021/jo00431a046
- Ugi, I. Angew. Chem. Int. Ed. Engl. 1982, 21, 810. https://doi.org/10.1002/anie.198208101
- Schollkopf, U. Angew. Chem. Int. Ed. Engl. 1977, 16, 339 https://doi.org/10.1002/anie.197703393
- Effenberger, F.; Eichhorn, J. Tetrahedron: Asymmetry 1997, 8, 469. https://doi.org/10.1016/S0957-4166(96)00528-9
- Humber, L. G. J. Med. Chem. 1971, 14, 982. https://doi.org/10.1021/jm00292a024
- Iseki, K.; Mizuno, S.; Kuroki, Y.; Kobayashi, Y. Tetrahedron 1999, 55, 977. https://doi.org/10.1016/S0040-4020(98)01097-7
- Kobayashi, S.; Nishio, K. J. Org. Chem. 1994, 59, 6620. https://doi.org/10.1021/jo00101a021
- Kobayashi, S.; Yasuda, M.; Hachiya, I. Chemistry Lett. 1996, 407.
- Strazzolini, P.; Giumanini, A. G.; Cauci, S. Tetrahedron 1990, 46, 1081 https://doi.org/10.1016/S0040-4020(01)86676-X
- Blicke, F. F.; Lu, C.-J. J. Am. Chem. Soc. 1952, 74, 3933 https://doi.org/10.1021/ja01135a503
- Waki, J.; Meienhofer, J. J. Org. Chem. 1977, 42, 2019 https://doi.org/10.1021/jo00431a046
- Chen, F. M. F.; Benoiton, N. L. Synthesis 1979, 709
- Yale, H. L. J. Org. Chem. 1971, 36, 3238 https://doi.org/10.1021/jo00820a603
- Kisfaludy, L.; Laszlo, O. Synthesis 1987, 510
- Neveux, M.; Bruneau, C.; Dixneuf, P. H. J. Chem. Soc. Perkin Trans. I 1991, 1197
- Duczek, W.; Deutsch, J.; Vieth, S.; Niclas, H.-J. Synthesis 1996, 37
- Reddy, P. G.; Kumar, G. D. K.; Baskaran, S. Tetrahedron Lett. 2000, 41, 9149 https://doi.org/10.1016/S0040-4039(00)01636-1
- Fieser, L. F.; Jones, J. E. Org. Synth., Coll. Vol. III 1955, 590
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