Pure and Applied Chemistry

Pure Appl. Chem., 2009, Vol. 81, No. 2, pp. 247-253

http://dx.doi.org/10.1351/PAC-CON-08-08-02

Aminolithiation of carbon-carbon double bonds as a powerful tool in organic synthesis

References

• 1. (a). M. Shimano, A. I. Meyers. J. Am. Chem. Soc. 116, 6437 (1994); (http://dx.doi.org/10.1021/ja00093a055)
• 1. (b). F. Dumas, B. Mezrhab, J. d'Angelo. J. Org. Chem. 61, 2293 (1996); (http://dx.doi.org/10.1021/jo951414r)
• 1. (c). N. Asao, T. Shimada, T. Sudo, N. Tsukada, K. Yazawa, Y. S. Gyoung, T. Uyehara, Y. Yamamoto. J. Org. Chem. 62, 6274 (1997). (http://dx.doi.org/10.1021/jo970435d)
• 2. (a). J. M. Hawkins, G. C. Fu. J. Org. Chem. 51, 2820 (1986); (http://dx.doi.org/10.1021/jo00364a041)
• 2. (b). S. G. Davies, O. Ichihara. Tetrahedron: Asymmetry 2, 183 (1991); (http://dx.doi.org/10.1016/S0957-4166(00)82354-X)
• 2. (c). D. Enders, H. Wahl, W. Bettray. Angew. Chem., Int. Ed. Engl. 34, 455 (1995); (http://dx.doi.org/10.1002/anie.199504551)
• 2. (d). S. G. Davies, A. D. Smith, P. D. Price. Tetrahedron: Asymmetry 16, 2833 (2005). (http://dx.doi.org/10.1016/j.tetasy.2005.08.006)
• 3. (a). M. Mizuno, K. Fujii, K. Tomioka. Angew. Chem., Int. Ed. Engl. 37, 515 (1998); (http://dx.doi.org/10.1002/(SICI)1521-3773(19980302)37:4<515::AID-ANIE515>3.0.CO;2-Q)
• 3. (b). M. Shindo, K. Koga, K. Tomioka. J. Org. Chem. 63, 9351 (1998); (http://dx.doi.org/10.1021/jo9813181)
• 3. (c). M. Iguchi, K. Tomioka. Org. Lett. 4, 4329 (2002). (http://dx.doi.org/10.1021/ol0269749)
• 4. Y. Yamamoto, H. Suzuki, Y. Yasuda, A. Iida, K. Tomioka. Tetrahedron Lett. 49, 4582 (2008). (http://dx.doi.org/10.1016/j.tetlet.2008.05.101)
• 5. H. Doi, T. Sakai, M. Iguchi, K. Yamada, K. Tomioka. J. Am. Chem. Soc. 125, 2886 (2003). (http://dx.doi.org/10.1021/ja029633z)
• 6. H. Doi, T. Sakai, K. Yamada, K. Tomioka. Chem. Commun. 1850 (2004). (http://dx.doi.org/10.1039/b405347h)
• 7. T. Sakai, H. Doi, Y. Kawamoto, K. Yamada, K. Tomioka. Tetrahedron Lett. 45, 9261 (2004). (http://dx.doi.org/10.1016/j.tetlet.2004.10.050)
• 8. T. Sakai, H. Doi, K. Tomioka. Tetrahedron 62, 8351 (2006). (http://dx.doi.org/10.1016/j.tet.2006.06.040)
• 9. N. Yasuda, Y. Hsiao, M. S. Jensen, N. R. Rivera, C. Yang, M. Wells, J. Yau, M. Palucki, L. Tan, P. G. Dormer, R. P. Volante, D. L. Hughes, P. J. Reider, J. Org. Chem. 69, 1959 (2004). (http://dx.doi.org/10.1021/jo030297u)
• 10. T. Sakai, Y. Kawamoto, K. Tomioka. J. Org. Chem. 71, 4706 (2006). (http://dx.doi.org/10.1021/jo060588d)
• 11. T. Sakai, K. Yamada K. Tomioka. Chem. Asian J. 3, 1486 (2008). (http://dx.doi.org/10.1002/asia.200700423)
• 12. T. Ogata, A. Ujihara, S. Tsuchida, T. Shimizu, A. Kaneshige, K. Tomioka. Tetrahedron Lett. 48, 6648 (2007). (http://dx.doi.org/10.1016/j.tetlet.2007.07.117)
• 13. S. Tsuchida, A. Kaneshige, T. Ogata, H. Baba, Y. Yamamoto, K. Tomioka. Org. Lett. 10, 3635 (2008). (http://dx.doi.org/10.1021/ol801397v)