Pure and Applied Chemistry

Pure Appl. Chem., 2010, Vol. 82, No. 9, pp. 1845-1853

http://dx.doi.org/10.1351/PAC-CON-09-09-40

Published online 2010-05-30

Enantioselective reactions catalyzed by chiral pyridine 2,6-bis(5',5'-diphenyloxazoline)-metal complexes

References

• 1a. A. Pfaltz. Acc. Chem. Res. 26, 339 (1993). (http://dx.doi.org/10.1021/ar00030a007)
• 1b. A. K. Ghosh, P. Mathivanan, J. Cappiello. Tetrahedron: Asymmetry 9, 1 (1998). (http://dx.doi.org/10.1016/S0957-4166(97)00593-4)
• 1c. D. A. Evans, T. Rovis, J. S. Johnson. Pure Appl. Chem. 71, 1407 (1999). (http://dx.doi.org/10.1351/pac199971081407)
• 1d. J. S. Johnson, D. A. Evans. Acc. Chem. Res. 33, 325 (2000). (http://dx.doi.org/10.1021/ar960062n)
• 1e. D. Rechavi, M. Lemaire. Chem. Rev. 102, 3467 (2002). (http://dx.doi.org/10.1021/cr020008m)
• 1f. H. A. MacManus, P. J. Guiry. Chem. Rev. 104, 4151 (2004). (http://dx.doi.org/10.1021/cr040642v)
• 1g. G. Desimoni, G. Faita, K. A. Jørgensen. Chem. Rev. 106, 3561 (2006). (http://dx.doi.org/10.1021/cr0505324)
• 1h. G. C. Hargaden, P. J. Guiry. Chem. Rev. 109, 2505 (2009). (http://dx.doi.org/10.1021/cr800400z)
• 2. H. Nishiyama, H. Sakaguchi, T. Nakamura, M. Horihata, M. Kondo, K. Itoh. Organometallics 8, 846 (1989). (http://dx.doi.org/10.1021/om00105a047)
• 3a. A. DattaGupta, D. Bhuniya, V. K. Singh. Tetrahedron 50, 13725 (1994). (http://dx.doi.org/10.1016/S0040-4020(01)85684-2)
• 3b. A. DattaGupta, V. K. Singh. Unpublished result.
• 4a. A. DattaGupta, V. K. Singh. Tetrahedron Lett. 37, 2633 (1996). (http://dx.doi.org/10.1016/0040-4039(96)00347-4)
• 4b. G. Sekar, A. DattaGupta, V. K. Singh. J. Org. Chem. 63, 2961 (1998). (http://dx.doi.org/10.1021/jo972132p)
• 4c. S. K. Ginotra, V. K. Singh. Tetrahedron 62, 3573 (2006). (http://dx.doi.org/10.1016/j.tet.2006.01.093)
• 4d. S. K. Ginotra, V. K. Singh. Org. Biomol. Chem. 4, 4370 (2006). (http://dx.doi.org/10.1039/b612423b)
• 5a. A. Bisai, V. K. Singh. Org. Lett. 8, 2405 (2006). (http://dx.doi.org/10.1021/ol060793f)
• 5b. A. Bisai, V. K. Singh. Unpublished result.
• 6. P. K. Singh, A. Bisai, V. K. Singh. Tetrahedron Lett. 48, 1127 (2007). (http://dx.doi.org/10.1016/j.tetlet.2006.12.081)
• 7a. S. Barroso, G. Blay, J. R. Pedro. Org. Lett. 9, 1983 (2007). (http://dx.doi.org/10.1021/ol0705752)
• 7b. S. Barroso, G. Blay, M. C. Muñoz, J. R. Pedro. Adv. Synth. Catal. 351, 107 (2009). (http://dx.doi.org/10.1002/adsc.200800606)
• 8. P. K. Singh, V. K. Singh. Org. Lett. 10, 4121 (2008). (http://dx.doi.org/10.1021/ol8016929)
• 9. Y. Liu, D. Shang, X. Zhou, X. Liu, X. Feng. Chem.—Eur. J. 15, 2055 (2009). (http://dx.doi.org/10.1002/chem.200802210)
• 10a. J. Lu, S.-J. Ji, Y.-C. Teo, T.-P. Loh. Org. Lett. 7, 159 (2005). (http://dx.doi.org/10.1021/ol047711c)
• 10b. J. Lu, S.-J. Ji, T.-P. Loh. Chem. Commun. 2345 (2005). (http://dx.doi.org/10.1039/b500086f)
• 10c. J. Lu, M.-L. Hong, S.-J. Ji, Y.-C. Teo, T.-P. Loh. Chem. Commun. 4217 (2005). (http://dx.doi.org/10.1039/b507768k)
• 10d. J. Lu, S.-J. Ji, Y.-C. Teo, T.-P. Loh. Tetrahedron Lett. 46, 7435 (2005). (http://dx.doi.org/10.1016/j.tetlet.2005.08.090)
• 10e. W.-Y. Chen, X.-S. Li. Lett. Org. Chem. 4, 398 (2007). (http://dx.doi.org/10.2174/157017807781467605)
• 11. R. Dodda, C.-G. Zhao. Tetrahedron Lett. 48, 4339 (2007). (http://dx.doi.org/10.1016/j.tetlet.2007.04.124)