DOI QR코드

DOI QR Code

Discrimination of Primary Alkyl and Arylamines by a New Binaphthyl-Azacrown-Anthracene Fluorophore

  • Lee, Kyu-Jung (Department of Chemistry and Chemistry Institute for Functional Materials, Pusan National University) ;
  • Li, Yinan (Department of Chemistry and Chemistry Institute for Functional Materials, Pusan National University) ;
  • Kim, Kwang-Soo (Department of Chemistry and Chemistry Institute for Functional Materials, Pusan National University) ;
  • Hyun, Myung-Ho (Department of Chemistry and Chemistry Institute for Functional Materials, Pusan National University)
  • Published : 2010.04.20

Abstract

Keywords

References

  1. Jiang, W.; Fu, Q.; Fan, H.; Ho, J.; Wang, W. Angew. Chem. Int. Ed.2007, 46, 8445. https://doi.org/10.1002/anie.200702271
  2. Vineis, P.; Pirastu, R. Cancer Causes and Control 1997, 8, 346. https://doi.org/10.1023/A:1018453104303
  3. Freudenthal, R. I.; Stephens, E.; Anderson, D. P. Internl. J. Tocol. 1999, 18, 353.
  4. Felknor, S. A.; Delclos, G. L.; Lerner, S.P.; Burau, K. D.; Wood, S. M.; Lusk, C. M.; Jalayer, A. D. J. Occup. Environ. Med. 2003, 45, 289. https://doi.org/10.1097/01.jom.0000052951.59271.73
  5. Oda, Y. Mutation Res. 2004, 554, 399. https://doi.org/10.1016/j.mrfmmm.2004.06.033
  6. Hauri, U.; Lutolf, B.; Schlegel, U.; Hohl, C. Mitt. Lebensm. Hyg. 2005, 96, 321.
  7. Kellen, E.; Zeegers, M.; Paulussen, A.; Vlietinck, R.; Vlem, E. V.; Veulemans, H.; Buntinx, F. Cancer Lett. 2007, 245, 51. https://doi.org/10.1016/j.canlet.2005.12.025
  8. Shiraishi, Y.; Sumiya, S.; Kohno, Y.; Hirai, T. J. Org. Chem.2008, 73, 8571. https://doi.org/10.1021/jo8012447
  9. Wang, F.; Peng, R.; Sha, Y. Molecules 2008,13, 922. https://doi.org/10.3390/molecules13040922
  10. Atilgan, S.; Ozdemir, T.; Akkaya, E. U. Org. Lett.2008, 10, 4065. https://doi.org/10.1021/ol801554t
  11. Kim, H. J.; Kim, S. H.; Kim, J. H.; Lee, E.-H.;Kim, K.-W.; Kim, J. S. Bull. Korean Chem. Soc. 2008, 29, 1831. https://doi.org/10.5012/bkcs.2008.29.9.1831
  12. Moczar, I.; Huszthy, P.; Maidics, Z.; Kadar, M.; Toth, K. Tetrahedron2009, 65, 8250. https://doi.org/10.1016/j.tet.2009.07.061
  13. Huang, J.; Xu, Y.; Qian, X. J. Org. Chem. 2009, 74, 2167. https://doi.org/10.1021/jo802297x
  14. Xu, Z.; Kim, G.-H.; Han, S. J.; Jou, M. J.;Lee, C.; Shin, I.; Yoon, J. Tetrahedron 2009, 65, 2307. https://doi.org/10.1016/j.tet.2009.01.035
  15. Kwon,S. K.; Kim, H. N.; Rho, J. H.; Swamy, K. M. K.; Shanthakumar,S. M.; Yoon, J. Bull. Korean Chem. Soc. 2009, 30, 719. https://doi.org/10.5012/bkcs.2009.30.3.719
  16. Sun, X. H.; Li, W.; Xia, P. F.; Luo, H.-B.; Wei, Y.; Wong, M.S.; Cheng, Y.-K.; Shuang, S. J. Org. Chem. 2007, 72, 2419. https://doi.org/10.1021/jo062258z
  17. Garcia-Garrido, S. E.; Caltagirone, C.; Light, M. E.; Gale, P. A. Chem. Commun. 2007, 1450.
  18. Kim, D.-S.; Ahn, K. H. J. Org. Chem. 2008, 73, 6831. https://doi.org/10.1021/jo801178y
  19. Kumar, S.; Luxami, V.; Kumar, A. Org. Lett. 2008, 10, 5549. https://doi.org/10.1021/ol802352j
  20. Chen, K.-H.; Liao, J.-H.; Chan, H.-Y.; Fang, J.-M. J. Org. Chem. 2009, 74, 895. https://doi.org/10.1021/jo802173b
  21. Jeon, N. J.; Ryu, B.J.; Lee, B. H.; Nam, K. C. Bull. Korean Chem. Soc. 2009, 30, 1675. https://doi.org/10.5012/bkcs.2009.30.7.1675
  22. Lin, J.; Zhang, H.-C.; Pu, L. Org. Lett. 2002, 4, 3297-3300. https://doi.org/10.1021/ol026565c
  23. Li, Z.-B.; Lin, J.; Qin, Y.-C.; Pu, L. Org. Lett. 2005, 7, 3441. https://doi.org/10.1021/ol0510163
  24. Xu, K.-X.; Wu, X.-J.; He, Y.-B.; Liu, S.-Y.; Qing, G.-Y.; Meng,L.-Z. Tetrahedron Assymetry 2005, 16, 833. https://doi.org/10.1016/j.tetasy.2004.12.023
  25. Kim, Y. K.; Lee,H. N.; Singh, N. J.; Choi, H. J.; Xue, J. Y.; Kim, K. S.; Yoon, J.; Hyun, M. H. J. Org. Chem. 2008, 73, 301. https://doi.org/10.1021/jo7022813
  26. Kim, K. S.; Jun, E. J.; Kim, S. K.; Choi, H. J.; Yoo, J.; Lee, C.-H.;Hyun, M. H.; Yoon, J. Tetrahedron Lett. 2007, 48, 2481. https://doi.org/10.1016/j.tetlet.2007.02.028
  27. Grun, A.; Koszegi, E.; Bitter, I. Tetrahedron 2004, 60, 5041. https://doi.org/10.1016/j.tet.2004.04.020
  28. Koszegi, E.; Grun, A.; Bitter, I. Supramol. Chem. 2006, 18, 67. https://doi.org/10.1080/10610270500373246
  29. Torrado, A.; Imperiali, B. J. Org. Chem. 1996, 61, 8940. https://doi.org/10.1021/jo961466w
  30. Benesi, H. A.; Hildebrand, J. H. J. Am. Chem. Soc. 1949, 71,2703. https://doi.org/10.1021/ja01176a030
  31. Rose, N. J.; Drago, R. S. J. Am. Chem. Soc. 1959, 81, 6138. https://doi.org/10.1021/ja01532a009
  32. de Silva, A. P.; Ripasinghe, R. A. D. D. J. Chem. Soc. Chem. Commun.1985, 1669.

Cited by

  1. Solvent-sensitive signs and magnitudes of circularly polarised luminescence and circular dichroism spectra: probing two phenanthrenes as emitters endowed with BINOL derivatives vol.16, pp.7, 2018, https://doi.org/10.1039/C7OB02308A