Bulletin of the Korean Chemical Society

  • 제30권12호
  • /
  • Pages.3082-3084
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  • 2009
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Pd(OAc)2 Immobilized on Fe3O4 as Magnetically Separable Heteogeneous Catalyst for Suzuki Reaction in Water

  • Jung, Ji-Young (Department of Chemical Science and Engineering, Inha University) ;
  • Kim, Jin-Beom (Department of Chemical Science and Engineering, Inha University) ;
  • Taher, Abu (Department of Chemical Science and Engineering, Inha University) ;
  • Jin, Myung-Jong (Department of Chemical Science and Engineering, Inha University)
  • 발행 : 2009.12.20
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참고문헌

  1. For reviews, see: (a) Kotha, S.; Lahiri, K.; Kashinath, D. Tetrahedron 2002, 58, 9633.(Please refer to the other references for details:no.9-no.10) https://doi.org/10.1016/S0040-4020(02)01188-2
  2. (a) Billingsley, K. L.; Buchwald, S. L. Angew. Chem. Int. Ed. 2008, 47, 4695.(Please refer to the other references for details:no.11-no.13) https://doi.org/10.1002/anie.200801465
  3. (a) Hardy, J. J. E.; Hubert, S.; Macquarrie, D. J.; Wilson, A. J.Green Chem. 2004, 6, 53.(Please refer to the other references for details:no.14-no.17) https://doi.org/10.1039/b312145n
  4. (a) Jain, N.; Kumar, A.; Chauhan, S.; Chauhan, S. M. S. Tetrahedron 2005, 61, 1015.(Please refer to the other references for details:no.18-no.19) https://doi.org/10.1016/j.tet.2004.10.070
  5. (a) Mehnert, C. P. Chem. Eur. J. 2005, 11, 50.(Please refer to the other references for details:no.20-no.21) https://doi.org/10.1002/chem.200400683
  6. (a) Tsang, S. C.; Caps, V.; Paraskevas, I.; Chadwick, D.; Thompsett, D. Angew. Chem. Int. Ed. 2004, 43, 5645.(Please refer to the other references for details:no.22-no.26) https://doi.org/10.1002/anie.200460552
  7. Brenna, S.; Posset, T.; Furrer, J.; Blumel, J. Chem. Eur. J. 2006, 12, 2880 https://doi.org/10.1002/chem.200501193
  8. Yin, L.; Liebscher, J. Chem. Rev. 2007, 107, 133 https://doi.org/10.1021/cr0505674
  9. (b) Nicolaou, K. C.; Bulger, P. G.; Sarlah, D. Angew. Chem. Int. Ed. 2005, 44, 4442. https://doi.org/10.1002/anie.200500368
  10. (c) Phan, N. T. S.; Sluys, M. V. D.; Jones C. W. Adv. Synth. Catal. 2006, 348, 609. https://doi.org/10.1002/adsc.200505473
  11. (b) Phan, N. T. S.; Styring, P. Green. Chem. 2008, 10, 1055. https://doi.org/10.1039/b805290e
  12. (c) Suzuki, K.; Sawaki, T.; Hori, Y.; Kobayashi, T. Synlett 2008, 12, 1809. https://doi.org/10.1055/s-2008-1078525
  13. (d) Zotto, A. D.; Amoroso, F.; Baratte, W.; Rigo, P.; Eur. J. Org. Chem. 2009, 110. https://doi.org/10.1002/ejoc.200800874
  14. (b) Kim, Y.-M.; Jin, M.-J. Bull. Korean Chem. Soc. 2005, 26, 373. https://doi.org/10.5012/bkcs.2005.26.3.373
  15. (c) Yang, Q.; Ma, S.; Li, J.; Xiao, F.; Xiong, H. Chem. Commun. 2006, 2495. https://doi.org/10.1039/b605733k
  16. (d) Sayah, R.; Glegola, K.; Framery, E.; Dufaud, V. Adv. Synth. Catal. 2007, 349, 373. https://doi.org/10.1002/adsc.200600286
  17. (e) Qiu, H.; Sarkar, S. M.; Lee, D.-H.; Jin, M.-J. Green Chem. 2008, 10, 37. https://doi.org/10.1039/b712624g
  18. (b) Akiyama, T.; Suzuki, A.; Fuchibe, K. Synlett 2005, 1024. https://doi.org/10.1055/s-2005-864816
  19. (c) Ranu, B. C.; Banerjee, S.; Jana, R. Tetrahedron 2007, 63, 776. https://doi.org/10.1016/j.tet.2006.10.077
  20. (b) Hagiwara, H.; Ko, K. H.; Hoshi, T.;Suzuki, T. Chem. Commun. 2007, 2838. https://doi.org/10.1039/b704098a
  21. (c) Jung, J.-Y.; Taher, A.; Kim, H.-J.; Ahn, W.-S. Synlett 2009, 39.
  22. (b) Hu, A.; Yee, T. G.; Lin, W. J. Am. Chem. Soc. 2005, 127, 12486. https://doi.org/10.1021/ja053881o
  23. (c) Dalaigh, C.; Corr, S. A.; Gun'ko, Y.; Connon, S. J. Angew. Chem., Int. Ed. 2007, 46, 4329. https://doi.org/10.1002/anie.200605216
  24. (d) Ge, J.; Huynh, T.; Hu, Y.; Yin, Y. Nano Lett 2008, 8, 931. https://doi.org/10.1021/nl080020f
  25. (e) Schatz, A.; Hager, M.; Reiser, O. Adv. Funct. Mater. 2009, 19, 2109. https://doi.org/10.1002/adfm.200801861
  26. (f) Shylesh, S.; Schweizer, J.; Demeshko, S.; Schunemann, V.; Ernst, S.; Thiel, W. R. Adv. Synth. Catal. 2009, 351, 1789. https://doi.org/10.1002/adsc.200900416

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  14. as Magnetically Separable Heterogeneous Catalyst for Suzuki Reaction in Water. vol.41, pp.18, 2010, https://doi.org/10.1002/chin.201018085
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  17. Iron Oxide Nanoparticles: An Efficient Nano-catalyst vol.23, pp.9, 2009, https://doi.org/10.2174/1385272823666190314153208
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