References
- Ogilvie, K. K.; Cheriyan, U. O.; Radatus, B. K.; Smith, K. O.;Galloway, K. S.; Kennell, W. L. Can. J. Chem. 1982, 60, 3005. https://doi.org/10.1139/v82-430
- Field, A. K.; Davie, M. E.; Dewitt, C.; Perry, H. C.; Liou, R.,Germershausen, J. I.; Karkas, J. D.; Ashton, W. T.; Johnson, D. B.R.; Tolman, R. C. Proc. Natl. Acad. Sci. (USA) 1983, 80, 4139. https://doi.org/10.1073/pnas.80.13.4139
- Martin, J. C.; Dvorak, C. A; Smee, D. F.; Mattews T. R.;Verheyden, J. P. H. J. Med. Chem. 1983, 26, 759. https://doi.org/10.1021/jm00359a023
- Ashton, W. T.; Canning, L. D.; Reynolds, G. F.; Tolman, R. L.;Karkas, J. D.; Liou, R., Davies, M. -E. M.; De Witt, C. M.; PerryH. C.; Field, A. K. J. Med. Chem. 1985, 28, 926. https://doi.org/10.1021/jm00145a014
- Lin, T. -S.; Lin, M. -C. Tetrahedron Lett. 1984, 25, 905. https://doi.org/10.1016/S0040-4039(01)80058-7
- Mac Coss, M.; Chen, A.; Tolman, R. L. Tetrahedron Lett. 1985, 26, 4287. https://doi.org/10.1016/S0040-4039(00)98714-8
- Riley, T. A.; Larson, S. B.; Avery, T. L.; Finch, R. A.; Robins, R.K. J. Med. Chem. 1990, 33, 572-576. https://doi.org/10.1021/jm00164a016
- Tanaka, H.; Fukui, M.; Hanaguchi, K.; Maskai, M.; Miyasaka, T.Tetrahedron Lett. 1989, 30, 2567. https://doi.org/10.1016/S0040-4039(01)80452-4
- Lazrek, H. B.; Engels, J. W.; Pfleiderer, W. Nucl. Nucl. 1988, 17,1851.
- Hibbert, H.; Carter, N. M. J. Chem. Soc., 1928, 50, 3120. https://doi.org/10.1021/ja01398a039
- Lazrek, H. B.; Khaider, H.; Rochdi, A.; Barascut, J. L.; Imbach, J.L. Tetrahedron Lett. 1996, 37, 4701. https://doi.org/10.1016/0040-4039(96)00910-0
- Yamamoto, I.; Sekine, M.; Hata, T. J. Chem. Soc. Perkin I 1980,306-310. https://doi.org/10.1039/p19800000306
- L'abbe, G.; Hassner, A. Bull. Soc. Chim. Belg. 1971, 80, 209. https://doi.org/10.1002/bscb.19710800124
- L'abbe, G.; Galle, J. E.; Hassner, A. Tetrahedron Lett. 1970, 303-306.
- Elguero, J.; Gonzàlez, E.; Jacquier, R. Bull. Soc. Chim. France1967, 2998-3003.
- Alonso, G.; Garcia-Lôpez, M. T. Garcia-Munoz, G.; Madrenero,R.; Rico, J. J. Heterocyclic Chem. 1970, 7, 1269. https://doi.org/10.1002/jhet.5570070606
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