References
- Triggle, D. J. In Comprehensive Medicinal Chemistry; Emmett, J. C., Volume Editor; Pergamon: Oxford, 1990; Vol. 3, Chapter 14.1.
- Bocker, R. H.; Guengerich, F. P. J. Med. Chem. 1986, 29, 1596. https://doi.org/10.1021/jm00159a007
- Guengerich, F. P.; Brian, W. R.; Iwasaki, M.; Sari, M.-A.; Baarnhielm, C.; Berntsson, P. J. Med. Chem. 1991, 34, 1838. https://doi.org/10.1021/jm00110a012
- Garcia, O.; Delgado, F.; Cano, A. C.; Alvarez, C. Tetrahedron Lett. 1993, 34, 623. https://doi.org/10.1016/S0040-4039(00)61635-0
- Sausins, A.; Duburs, G. Heterocycles 1988, 27, 291.
- Vanden Eynde, J.-J.; Mayence, A.; Maquestiau, A. Tetrahedron 1992, 48, 463. https://doi.org/10.1016/S0040-4020(01)89008-6
- Ko, K.-Y.; Park, J.-Y. Bull. Korean Chem. Soc. 1995, 16, 200.
- Maquestiau, A.; Mayence, A.; Vanden Eynde, J.-J. Tetrahedron Lett. 1991, 32, 3839.
- Pfister, J. R. Synthesis 1990, 689.
- Vanden Eynde, J.-J.; Delfosse, F.; Mayence, A.; Van Haverbeke, Y. Tetrahedron 1995, 51, 6511. https://doi.org/10.1016/0040-4020(95)00318-3
- Vanden Eynde, J.-J.; D'Orazio, R.; Van Haverbeke, Y. Tetrahedron 1994, 50, 2479. https://doi.org/10.1016/S0040-4020(01)86964-7
- Itoh, T.; Nagata, K.; Okada, M.; Ohsawa, A. Tetrahedron Lett. 1995, 36, 2269. https://doi.org/10.1016/0040-4039(95)00268-H
- Mashraqui, S. H.; Karnik, M. A. Synthesis 1997, 713.
- Mashraqui, S. H.; Karnik, M. A. Tetrahedron Lett. 1998, 39, 4895. https://doi.org/10.1016/S0040-4039(98)00889-2
- Varma, R. S.; Kumar, D. Tetrahedron Lett. 1999, 40, 21. https://doi.org/10.1016/S0040-4039(98)80007-5
- Jin, M.-Z.; Yang, L.; Wu, L.-M.; Liu, Y.-C.; Liu, Z.-L. Chem. Commun. 1998, 2451.
- Yadav, J. S.; Subba Reddy, B. V.; Sabitha, G.; Kiran Kumar Reddy, G. S. Synthesis 2000, 1532.
- Ko, K.-Y.; Kim, J.-Y. Tetrahedron Lett. 1999, 40, 3207. https://doi.org/10.1016/S0040-4039(99)00467-0
- Moriarty, R. M.; Vaid, R. K.; Koser, G. F. Synlett 1990, 365.
- Koser, G. F. Aldrichimica Acta 2001, 34, 89.
- Varvoglis, A. Tetrahedron 1997, 53, 1179. https://doi.org/10.1016/S0040-4020(96)00970-2
- Varma, R. S.; Kumar, D. J. Chem. Soc., Perkin Trans. 1 1999, 1755.
- Nicolaou, K. C.; Montagnon, T.; Baran, P. S.; Zhong, Y.-L. J. Am. Chem. Soc. 2002, 124, 2245. https://doi.org/10.1021/ja012127+
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