Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Asymmetric Synthesis of Aziridines and Arylalanine Derivatives

  • Published : 2005.02.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Osborn, H. M. I.; Sweeney, J. Tetrahedron: Asymmetry 1997, 8, 1693 https://doi.org/10.1016/S0957-4166(97)00177-8
  2. Tanner, D. Angew. Chem. Int. Ed. Engl. 1994, 33, 599 https://doi.org/10.1002/anie.199405991
  3. Jacobsen, E. N. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Ed.; Springer-Verlag: Berlin, Heidelberg, New York, 1999; Vol. 2, p 607
  4. Atkinson, R. S. Tetrahedron 1999, 55, 1519 https://doi.org/10.1016/S0040-4020(98)01199-5
  5. Cardillo, G.; Gentilucci, L.; Tolomelli, A. Aldrichimica Acta 2003, 36, 57
  6. Yadav, J. S.; Reddy, B. V. S.; Rao, M. S.; Reddy, P. N. Tetrahedron Lett. 2003, 44, 5275 https://doi.org/10.1016/S0040-4039(03)01264-4
  7. Antilla, J. C.; Wulff, W. D. J. Am. Chem. Soc. 1999, 121, 5099 https://doi.org/10.1021/ja9905187
  8. Loncaric, C.; Wulff, W. D. Org. Lett. 2001, 3, 3675 https://doi.org/10.1021/ol010180x
  9. Casarrubios, L.; Perez, J. A.; Brookhart, M.; Templeton, J. L. J. Org. Chem. 1996, 61, 8358 https://doi.org/10.1021/jo961391w
  10. Ha, H.-J.; Kang, K.-H.; Suh, J.-M.; Ahn, Y.-G. Tetrahedron Lett. 1996, 37, 7069 https://doi.org/10.1016/0040-4039(96)01554-7
  11. Sengupta, S.; Mondal, S. Tetrahedron Lett. 2000, 41, 6245 https://doi.org/10.1016/S0040-4039(00)01042-X
  12. Juhl, K.; Hazell, R. G.; Jorgensen, K. A. J. Chem. Soc. Perkin Trans. 1 1999, 2293
  13. Lee, S.-H.; Han, T.-D.; Yu, K. A.; Ahn, K.-H. Bull. Korean Chem. Soc. 2000, 22, 449
  14. Rasmussen, K. G.; Jorgensen, K. A. J. Chem. Soc., Perkin Trans. 1 1997, 1287
  15. Mayer, M. F.; Hossain, M. M. J. Org. Chem. 1998, 63, 6839 https://doi.org/10.1021/jo9804792
  16. Kubo, T.; Sakasguchi, S.; Ishii, Y. Chem. Commun. 2000, 625
  17. Nagayama, S.; Kobayashi, S. Chem. Lett. 1998, 685
  18. Xie, W.; Fang, J.; Li, J.; Wang, P. G. Tetrahedron 1999, 55, 12929 https://doi.org/10.1016/S0040-4020(99)00791-7
  19. Chang, J.-W.; Bae, J. H.; Shin, S.-H.; Park, C. S.; Choi, D.; Lee, W. K. Tetrahedron Lett. 1998, 39, 9193 https://doi.org/10.1016/S0040-4039(98)02095-4

Cited by

  1. Recent Advances in the Stereoselective Synthesis of Aziridines vol.114, pp.16, 2014, https://doi.org/10.1021/cr400553c
  2. Diastereoselective formation of aziridines from diazocarbonyl compounds and N-(O-pivaloylated d-galactosyl)benzylideneamines and ring-opening reactions with p-toluenethiol vol.12, pp.21, 2014, https://doi.org/10.1039/c4ob00443d
  3. Asymmetric Synthesis of Aziridines and Arylalanine Derivatives. vol.36, pp.26, 2005, https://doi.org/10.1002/chin.200526057
  4. -Arylaziridine Carboxylates vol.351, pp.16, 2009, https://doi.org/10.1002/adsc.200900474
  5. Highly Diastereoselective Alkylation of Aziridine-2-carboxylate Esters: Enantioselective Synthesis of LFA-1 Antagonist BIRT-377 vol.117, pp.38, 2005, https://doi.org/10.1002/ange.200500923
  6. Highly Diastereoselective Alkylation of Aziridine-2-carboxylate Esters: Enantioselective Synthesis of LFA-1 Antagonist BIRT-377 vol.44, pp.38, 2005, https://doi.org/10.1002/anie.200500923
  7. Application of Microwave Activation Techniques to the N-Alkenyl Protection of Lactams vol.27, pp.2, 2005, https://doi.org/10.5012/bkcs.2006.27.2.286
  8. Recent developments in asymmetric aziridination vol.66, pp.8, 2005, https://doi.org/10.1016/j.tet.2009.11.089
  9. Double Stereodifferentiation in the Catalytic Asymmetric Aziridination of Imines Prepared from α‐Chiral Amines vol.18, pp.17, 2005, https://doi.org/10.1002/chem.201102520