Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Alkylselenite-catalyzed Oxidative Carbonylation of Amines: Density Functional Theory Study

  • Hwang, Sun (Department of Chemistry and Research Institute of Basic Sciences, Kyung Hee University) ;
  • Kim, Hoon Sik (Department of Chemistry and Research Institute of Basic Sciences, Kyung Hee University) ;
  • Cheong, Minserk (Department of Chemistry and Research Institute of Basic Sciences, Kyung Hee University)
  • Received : 2012.07.30
  • Accepted : 2012.09.03
  • Published : 2012.11.20
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Abstract

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References

  1. Macho, V.; Harustiak, M. J. Mol. Catal. 1994, 91, L155. https://doi.org/10.1016/0304-5102(94)00062-X
  2. Grate, J. H.; Hamm, D. R.; Valentine, D. H. U.S. Patent 4,600,793.
  3. Aresta, M.; Quaranta, E. J. Chem. Soc., Dalton Trans. 1992, 1893.
  4. Yoshida, Y.; Inoue, S. J. Chem. Soc., Perkin Trans. 1979, 1, 3146.
  5. Skoog, S. H.; Campbell, J. P.; Gladfelter, W. L. Organometallics 1994, 13, 4137. https://doi.org/10.1021/om00023a005
  6. Fukuoka, S.; Chono, M.; Kohno, M. CHEMTECH 1984, 670.
  7. Lee, C. W.; Lee, J. S.; Lee, S. M.; Kim, K. D.; Cho, N. S.; Oh, J. S. J. Mol. Catal. 1993, 81, 17. https://doi.org/10.1016/0304-5102(93)80019-Q
  8. Giannoccaro, P. J. Organomet. Chem. 1987, 336, 271. https://doi.org/10.1016/0022-328X(87)87174-7
  9. Tafesh, A. M.; Weiguny, J. Chem. Rev. 1996, 96, 2035. https://doi.org/10.1021/cr950083f
  10. Macho, V.; Kralik, M.; Halmo, F. J. Mol. Catal. A: Chem. 1996, 109, 119. https://doi.org/10.1016/1381-1169(96)00006-4
  11. Gargulak, J. D.; Gladfelter, W. L. J. Am. Chem. Soc. 1994, 116, 3792. https://doi.org/10.1021/ja00088a015
  12. Fournier, J.; Bruneau, C.; Dixneuf, P. H.; Lecolier, S. J. Org. Chem. 1991, 56, 4456. https://doi.org/10.1021/jo00014a024
  13. Li, K. T.; Peng, Y. J. J. Catal. 1993, 143, 631. https://doi.org/10.1006/jcat.1993.1306
  14. Gupte, S. P.; Chaudhari, R. V. J. Catal. 1988, 114, 246.
  15. Gupte, S. P.; Chaudhari, R. V. Ind. Eng. Chem. Res. 1992, 31, 2069. https://doi.org/10.1021/ie00009a001
  16. Fukuoka, S.; Chono, M. J. Chem. Soc., Chem. Commun. 1984, 399.
  17. Fukuoka, S.; Chono, M.; Kohono, M. J. Org. Chem. 1984, 49, 1460. https://doi.org/10.1021/jo00182a036
  18. Alper, H.; Hartstock, F. W. J. Chem. Soc., Chem. Commun. 1985, 1141.
  19. Giannoccaro, P.; Nobile, C. F.; Moro, G. J. Mol. Catal. 1989, 53, 349. https://doi.org/10.1016/0304-5102(89)80067-7
  20. Desai, M. N.; Butt, J. B.; Dranoff, J. S. J. Catal. 1983, 79, 95. https://doi.org/10.1016/0021-9517(83)90292-0
  21. Ferragina, C.; Massucci, M. A.; Patrono, O.; La Ginestra, A.; Tomlinson, A. A. G. J. Chem. Soc., Dalton Trans. 1988, 851.
  22. Giannoccaro, P. Inorg. Chim. Acta 1988, 142, 81. https://doi.org/10.1016/S0020-1693(00)80662-3
  23. Gupte, S. P.; Mulla, S. A.; Rode, C. V.; Kelkar, A. A. J. Mol. Catal. A: Chem. 1997, 122, 103. https://doi.org/10.1016/S1381-1169(97)00023-X
  24. Kim, H. S.; Kim, Y. J.; Lee, H.; Park, K. Y.; Chin, C. S. J. Catal. 1998, 176, 264. https://doi.org/10.1006/jcat.1998.2074
  25. Kim, H. S.; Kim, Y. J.; Lee, H.; Lee, S. D.; Chin, C. S. J. Catal. 1999, 184, 526. https://doi.org/10.1006/jcat.1999.2458
  26. Kim, H. S.; Kim, Y. J.; Lee, H.; Park, K. Y.; Lee, C. M.; Chin, C. S. Angew. Chem., Int. Ed. 2002, 41, 4300. https://doi.org/10.1002/1521-3773(20021115)41:22<4300::AID-ANIE4300>3.0.CO;2-V
  27. Kim, H. S.; Kim, Y. J.; Bae, J. Y.; Kim, S. J.; Lah, M. S.; Chin, C. S. Organometallics 2003, 22, 2498. https://doi.org/10.1021/om030005f
  28. Cheong, M.; Schmid, R.; Ziegler, T. Organometallics 2000, 19, 1973. https://doi.org/10.1021/om9910221
  29. Frisch, M. J. et al. Gaussian 09, Revision A.1, Gaussian Inc., Wallingford, CT, USA, 2009.
  30. Khanna, R. K.; Moore, M. H. Spectrochim. Acta A: Mol. Biomol. Spectros. 1999, 55A, 961.
  31. Xie, H.-B.; Zhou, Y.; Zhang, Y.; Johnson, J. K. J. Phys. Chem. A 2010, 114, 11844. https://doi.org/10.1021/jp107516k
  32. Barzagli, F.; Mani, F.; Peruzzini, M. Energy Environ. Sci. 2010, 3, 772. https://doi.org/10.1039/b924889g

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