Pure Appl. Chem., 2007, Vol. 79, No. 2, pp. 163-172
http://dx.doi.org/10.1351/pac200779020163
Recent results toward the stereoselective synthesis of biologically active natural products
References
- 1. L. C. Dias, L. G. de Oliveira, J. D. Vilcachagua, F. Nigsch. J. Org. Chem. 70, 2225 (2005). (http://dx.doi.org/10.1021/jo047732k)
- 2. L. C. Dias, L. G. de Oliveira. Org. Lett. 3, 3951 (2001). (http://dx.doi.org/10.1021/ol016845c)
- 3. L. C. Dias, P. R. R. Meira. J. Org. Chem. 70, 4762 (2005). (http://dx.doi.org/10.1021/jo050352u)
- 4. R. Jansen, P. Washausen, B. Kunze, H. Reichenbach, G. Hofle. Eur. J. Org. Chem. 1085 (1999). (http://dx.doi.org/10.1002/(SICI)1099-0690(199905)1999:5<1085::AID-EJOC1085>3.0.CO;2-G)
- 5. (a). B. Kunze, R. Jansen, G. Hofle, H. Reichenbach. J. Antibiot. 47, 881 (1994);
- 5. (b). B. Kunze, R. Jansen, F. Sasse, G. Hofle, H. Reichenbach. J. Antibiot. 51, 1075 (1998).
- 6. (a). J. T. Feutrill, M. A. Rizzacasa. Aust. J. Chem. 56, 783 (2003); (http://dx.doi.org/10.1071/CH03026)
- 6. (b). T. K. Chakraborty, P. Laxman. Tetrahedron Lett. 44, 4989 (2003). (http://dx.doi.org/10.1016/S0040-4039(03)01171-7)
- 7. (a). J. T. Feutrill, M. J. Lilly, M. A. Rizzacasa. Org. Lett. 2, 3365 (2000); (http://dx.doi.org/10.1021/ol0064664)
- 7. (b). T. K. Chakraborty, S. Jayaprakash. Tetrahedron Lett. 42, 497 (2001); (http://dx.doi.org/10.1016/S0040-4039(00)02002-5)
- 7. (c). L. C. Dias, L. G. de Oliveira. Org. Lett. 3, 3951 (2001). (http://dx.doi.org/10.1021/ol016845c)
- 8. (a). J. T. Feutrill, M. J. Lilly, M. A. Rizzacasa. Org. Lett. 4, 525 (2002); (http://dx.doi.org/10.1021/ol017092x)
- 8. (b). T. K. Chakraborty, P. Laxman. Tetrahedron Lett. 43, 2645 (2002); (http://dx.doi.org/10.1016/S0040-4039(02)00289-7)
- 8. (c). L. C. Dias, L. G. de Oliveira, J. D. Vilcachagua, F. Nigsch. J. Org. Chem. 70, 2225 (2005). (http://dx.doi.org/10.1021/jo047732k)
- 9. (a). M. K. Gurjar, T. P. Khaladkar, R. G. Borhade, A. Murugan. Tetrahedron Lett. 44, 5183 (2003); (http://dx.doi.org/10.1016/S0040-4039(03)01256-5)
- 9. (b). S. Raghavan, R. Reddy. Tetrahedron Lett. 45, 5593 (2004); (http://dx.doi.org/10.1016/j.tetlet.2004.05.130)
- 9. (c). M. Besev, C. Brehm, A. Furstner. Collect. Czech. Chem. Commun. 70, 1696 (2005); (http://dx.doi.org/10.1135/cccc20051696)
- 9. (d). J. S. Yadav, P. V. Reddy, L. Chandraiah. Tetrahedron Lett. 48, 145 (2007). (http://dx.doi.org/10.1016/j.tetlet.2006.10.141)
- 10. (a). M. Isobe, M. Kitamura, S. Mio, T. Goto. Tetrahedron Lett. 23, 221 (1982); (http://dx.doi.org/10.1016/S0040-4039(00)86790-8)
- 10. (b). M. Kitamura, M. Isobe, Y. Ichikawa, Y. Goto. J. Org. Chem. 49, 3517 (1984); (http://dx.doi.org/10.1021/jo00193a015)
- 10. (c). K. Maruyama, M. Ueda, S. Sasaki, Y. Iwata, M. Miyazawa, M. Miyashita. Tetrahedron Lett. 39, 4517 (1998). (http://dx.doi.org/10.1016/S0040-4039(98)00804-1)
- 11. L. Jiang, G. E. Job, A. Klapars, S. P. Buchwald. Org. Lett. 5, 3667 (2003). (http://dx.doi.org/10.1021/ol035355c)
- 12. X. Pan, Q. Cai, D. Ma. Org. Lett. 6, 1809 (2004). (http://dx.doi.org/10.1021/ol049464i)
- 13. M. Kobayashi, K. Higuchi, N. Murakami, H. Tajima, S. Aoki. Tetrahedron Lett. 38, 2859 (1997). (http://dx.doi.org/10.1016/S0040-4039(97)00482-6)
- 14. N. Murakami, W. Wang, M. Aoki, Y. Tsutsui, K. Higuchi, S. Aoki, M. Kobayashi. Tetrahedron Lett. 38, 5533 (1997). (http://dx.doi.org/10.1016/S0040-4039(97)01194-5)
- 15. (a). T. Hamamoto, H. Seto, T. Beppu. J. Antibiot. 36, 646 (1983);
- 15. (b). Absolute stereochemistry and synthesis of leptomycin B: M. Kobayashi, W. Wang, Y. Tsutsui, M. Sugimoto, N. Murakami. Tetrahedron Lett. 39, 8291 (1998). (http://dx.doi.org/10.1016/S0040-4039(98)01809-7)
- 16. (a). N. Murakami, W. Wang, M. Aoki, Y. Tsutsui, M. Sugimoto, M. Kobayashi. Tetrahedron Lett. 39, 2349 (1998); (http://dx.doi.org/10.1016/S0040-4039(98)00151-8)
- 16. (b). M. T. Crimmins, B. W. King. J. Am. Chem. Soc. 120, 9084 (1998); (http://dx.doi.org/10.1021/ja9817500)
- 16. (c). A. B. Smith III, B. M. Brandt. Org. Lett. 3, 1685 (2001); (http://dx.doi.org/10.1021/ol0158922)
- 16. (d). M. Kalesse, M. Quitschalle, C. P. Khandavalli, A. Saeed. Org. Lett. 3, 3107 (2001); (http://dx.doi.org/10.1021/ol016365l)
- 16. (e). J. L. Vicario, A. Job, M. Wolberg, M. Muller, D. Enders. Org. Lett. 4, 1023 (2002); (http://dx.doi.org/10.1021/ol0256116)
- 16. (f). J. A. Marshall, M. P. Bourbeau. J. Org. Chem. 67, 2751 (2002); (http://dx.doi.org/10.1021/jo016025d)
- 16. (g). M. Lautens, T. A. Stammers. Synthesis 1993 (2002); (http://dx.doi.org/10.1055/s-2002-34386)
- 16. (h). M. Kalesse, K. P. Chary, M. Quitschalle, A. Burzlaff, C. Kasper, T. Scheper. Chem. Eur. J. 9, 1129 (2003); (http://dx.doi.org/10.1002/chem.200390130)
- 16. (i). N. F. Langille, J. S. Panek. Org. Lett. 6, 3203 (2004). (http://dx.doi.org/10.1021/ol048664r)
- 17. (a). N. Murakami, M. Sugimoto, M. Kobayashi. Bioorg. Med. Chem. 9, 57 (2001); (http://dx.doi.org/10.1016/S0968-0896(00)00220-0)
- 17. (b). N. Murakami, M. Sugimoto, T. Nakajima, M. Kawanishi, Y. Tsutsui, M. Kobayashi. Bioorg. Med. Chem. 8, 2651 (2000). (http://dx.doi.org/10.1016/S0968-0896(00)00199-1)
- 18. M. Kalesse, M. Christmann. Synthesis 981 (2002). (http://dx.doi.org/10.1055/s-2002-31946)
- 19. (a). L. C. Dias, P. R. R. Meira. Tetrahedron Lett. 43, 185 (2002); (http://dx.doi.org/10.1016/S0040-4039(01)02104-9)
- 19. (b). L. C. Dias, P. R. R. Meira. Tetrahedron Lett. 43, 8883 (2002). (http://dx.doi.org/10.1016/S0040-4039(02)02200-1)
- 20. (a). J. R. Gage, D. A. Evans. Org. Synth. 68, 83 (1990);
- 20. (b). D. A. Evans, J. Bartroli, T. L. Shih. J. Am. Chem. Soc. 103, 2127 (1981); (http://dx.doi.org/10.1021/ja00398a058)
- 20. (c). D. A. Evans, T. R. Taber. Tetrahedron Lett. 21, 4675 (1980). (http://dx.doi.org/10.1016/0040-4039(80)88091-9)
- 21. (a). H. Nagaoka, Y. Kishi. Tetrahedron 37, 3873 (1981); (http://dx.doi.org/10.1016/S0040-4020(01)93261-2)
- 21. (b). B. H. Lipshutz, J. Kozlowski, R. S. Wilhelm. J. Am. Chem. Soc. 104, 2305 (1982); (http://dx.doi.org/10.1021/ja00372a032)
- 21. (c). H. Kigoshi, K. Suenaga, T. Mutou, T. Ishigaki, T. Atsumi, H. Ishiwata, A. Sakakura, T. Ogawa, M. Ojika, K. Yamada. J. Org. Chem. 61, 5326 (1996). (http://dx.doi.org/10.1021/jo9606113)
- 22. K. Takai, K. Nitta, K. Utimoto. J. Am. Chem. Soc. 108, 7408 (1986). (http://dx.doi.org/10.1021/ja00283a046)
- 23. (a). J. A. Marshall, Z. H. Lu, B. A. Johns. J. Org. Chem. 63, 817 (1998); (http://dx.doi.org/10.1021/jo971900+)
- 23. (b). J. A. Marshall, B. A. Johns. J. Org. Chem. 63, 7885 (1998); (http://dx.doi.org/10.1021/jo9811423)
- 23. (c). N. Miyaura, A. Suzuki. Chem. Rev. 95, 2457 (1995); (http://dx.doi.org/10.1021/cr00039a007)
- 23. (d). C. R. Johnson, M. P. Braun. J. Am. Chem. Soc. 115, 11014 (1993). (http://dx.doi.org/10.1021/ja00076a079)
- 24. (a). D. B. Dess, J. C. Martin. J. Am. Chem. Soc. 113, 7277 (1991); (http://dx.doi.org/10.1021/ja00019a027)
- 24. (b). D. B. Dess, J. C. Martin. J. Org. Chem. 48, 4155 (1983); (http://dx.doi.org/10.1021/jo00170a070)
- 24. (c). R. E. Ireland, L. Liu. J. Org. Chem. 58, 2899 (1993). (http://dx.doi.org/10.1021/jo00062a040)