Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Molecular Recognition of Amino Sugars by a Porphyrin-based Receptor in Aqueous Media

  • Lee, Jung-Deog (Department of Chemistry, Seoul National University) ;
  • Jang, Dong-Hak (Department of Chemistry, Seoul National University) ;
  • Hong, Jong-In (Department of Chemistry, Seoul National University)
  • Received : 2010.07.15
  • Accepted : 2010.07.16
  • Published : 2010.09.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Lis, H.; Sharon, N. Chem. Rev. 1998, 98, 637-674. https://doi.org/10.1021/cr940413g
  2. Quiocho, F. A. Pure Appl. Chem. 1989, 61, 1293-1306. https://doi.org/10.1351/pac198961071293
  3. Lemieux, R. U. Chem. Soc. Rev. 1989, 18, 347-374. https://doi.org/10.1039/cs9891800347
  4. Lis, H.; Sharon, N. Lectins; Kluwer Academic Publishers: Dordrecht, The Netherlands, 2003.
  5. Dormitzer, P. R.; Sun, Z. Y.; Wagner, G.; Harrison, S. C. EMBO J. 2002, 21, 885-897. https://doi.org/10.1093/emboj/21.5.885
  6. Davis, A. P.; Wareham, R. S. Angew. Chem. Int. Ed. 1999, 38, 2978-2996. https://doi.org/10.1002/(SICI)1521-3773(19991018)38:20<2978::AID-ANIE2978>3.0.CO;2-P
  7. Mazik, M. Chem. Soc. Rev. 2009, 38, 935-956. https://doi.org/10.1039/b710910p
  8. Aoyama, Y. In Comprehensive Supramolecular Chemistry; Atwood, J. L., Davis, J. E. D., MacNicol, D. D., Vogtle, F., Eds.; Vol. 2, Pergamon: Oxford, 1996; pp 279-307.
  9. Lecollinet, G.; Dominey, A. P.; Velasco, T.; Davis, A. P. Angew. Chem. Int. Ed. 2002, 41, 4093-4096. https://doi.org/10.1002/1521-3773(20021104)41:21<4093::AID-ANIE4093>3.0.CO;2-I
  10. Velasco, T.; Lecollinet, G.; Ryan, T.; Davis, A. P. Org. Biomol. Chem. 2004, 2, 645-647. https://doi.org/10.1039/b315447e
  11. Welti, R.; Diederich, F. Helv. Chim. Acta 2003, 86, 494-503. https://doi.org/10.1002/hlca.200390049
  12. Abe, H.; Aoyagi, Y.; Inouye, M. Org. Lett. 2005, 7, 59-61. https://doi.org/10.1021/ol047907c
  13. Mazik, M.; Bandmann, H.; Sicking, W. Angew. Chem. Int. Ed. 2000, 39, 551-554. https://doi.org/10.1002/(SICI)1521-3773(20000204)39:3<551::AID-ANIE551>3.0.CO;2-7
  14. Mazik, M.; Cavga, H.; Jones, P. G. J. Am. Chem. Soc. 2005, 127, 9045-9052. https://doi.org/10.1021/ja043037i
  15. Ishi-i, T.; Mateos-Timoneda, M. A.; Timmerman, P.; Crego-Calama, M.; Reinhoudt, D. N.; Shinkai, S. Angew. Chem. Int. Ed. 2003, 42, 2300-2305. https://doi.org/10.1002/anie.200350956
  16. Kim, H.-J.; Kim, Y.-H.; Hong, J.-I. Tetrahedron Lett. 2001, 42, 5049-5052. https://doi.org/10.1016/S0040-4039(01)00915-7
  17. Cho, H.-K.; Kim, H.-J.; Lee, K.-H.; Hong, J.-I. Bull. Korean Chem. Soc. 2004, 25, 1714-1716. https://doi.org/10.5012/bkcs.2004.25.11.1714
  18. Lee, D.-H.; Kim, H.-J.; Hong, J.-I. Supramolecular Chemistry 2007, 19, 251-256. https://doi.org/10.1080/10610270701268799
  19. Klein, E.; Crump, M. P.; Davis, A. P. Angew. Chem. Int. Ed. 2005, 44, 298-302. https://doi.org/10.1002/anie.200461409
  20. Mazik, M.; Cavga, H.; Jones, P. G. J. Am. Chem. Soc. 2005, 127, 9045-9052. https://doi.org/10.1021/ja043037i
  21. Quiocho, F. A.; Wilson, D. K.; Vyas, N. K. Nature 1989, 340, 404. https://doi.org/10.1038/340404a0
  22. Kim, Y.-H.; Hong, J.-I. Angew. Chem. Int. Ed. 2002, 41, 2947-2950. https://doi.org/10.1002/1521-3773(20020816)41:16<2947::AID-ANIE2947>3.0.CO;2-H
  23. Ladomenou, K.; Bonar-Law, R. P. Chem. Commun. 2002, 2108-2109.
  24. Mazik, M.; Cavga, H. J. Org. Chem. 2006, 71, 2957-2963. https://doi.org/10.1021/jo052479p
  25. Mazik, M.; Cavga, H. Eur. J. Org. Chem. 2007, 3633-3638.
  26. Mazik, M.; Cavga, H. J. Org. Chem. 2007, 72, 831-838. https://doi.org/10.1021/jo061901e
  27. Mohamadi, F.; Richards, N. G. J.; Guida, W. C.; Liskamp, R.; Lipton, M.; Caufield, C.; Chang, G.; Hendrickson, T.; Still, W. C. J. Comput. Chem. 1990, 11, 440. https://doi.org/10.1002/jcc.540110405

Cited by

  1. Gold-Catalyzed Reactions of 2-C-Branched Carbohydrates: Mild Glycosidations and Selective Anomerizations vol.2011, pp.13, 2011, https://doi.org/10.1002/ejoc.201100134
  2. Absolute Stereochemical Determination of Chiral Carboxylates Using an Achiral Molecular Tweezer vol.18, pp.39, 2012, https://doi.org/10.1002/chem.201200371