Copper nanoparticles supported on silica coated maghemite as versatile, magnetically recoverable and reusable catalyst for alkyne coupling and cycloaddition reactions

Applied Catalysis A: General

Volumn 455, Issue , 2013, Pages 39-45

  Nador, F ^a   Volpe, M A ^b   Alonso, F ^c   Feldhoff, A ^d   Kirschning, A ^d   Radivoy, G ^a  

^a UNIVERSIDAD NACIONAL DEL SUR   (Argentina)

^b PLAPIQUI UNS CONICET   (Argentina)

^c UNIVERSITY OF ALICANTE   (Spain)

^d LEIBNIZ UNIVERSITY HANNOVER   (Germany)

Author keywords

Alkyne; Copper nanoparticles; Coupling; Cycloaddition; Magnetic support

Indexed keywords

1 ,3-DIPOLARCYCLOADDITION; ALKYNE; COPPER NANOPARTICLES; COPPER-BASED CATALYSTS; MAGHEMITE NANOPARTICLE; MAGNETIC SUPPORT; RECOVERABLE AND REUSABLE CATALYST; SOLVENT FREE CONDITIONS;

CATALYST ACTIVITY; COUPLINGS; CYCLOADDITION; HYDROCARBONS; METAL NANOPARTICLES; ORGANIC SOLVENTS; SILICA;

CATALYST SUPPORTS;

EID: 84875971203     PISSN: 0926860X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apcata.2013.01.023     Document Type: Article

References (51)

1. P.J. Walsh, and A. de Parradi Angew. Chem. Int. Ed. Engl. 48 2009 4679 4682
2. C. Glaser Ber. Dtsch. Chem. Ges. 2 1869 422 424
3. C. Glaser Ann. Chem. Pharm. 154 1870 137 171
4. L. Brandsma Synthesis of Acetylenes, Allenes and Cumulenes 2004 Elsevier Academic Press Amsterdam chapter 15
5. P. Siemsen, R.C. Livingston, and F. Diederich Angew. Chem. Int. Ed. 39 2000 2632 2657
6. F. Alonso, and M. Yus ACS Catal. 2 2012 1441 1451
7. L. Zani, and C. Bolm Chem. Commun. 2006 4263 4275
8. C. C.-J- Li Acc. Chem. Res. 43 2010 581 590
9. W.-J. Yoo, L. Zhao, and C.-J. Li Aldrichima Acta 44 2011 43 51
10. R. Huisgen, G. Szeimies, and L. Moebius Chem. Ber. 98 1965 4014 4021
11. R. Huisgen Pure Appl. Chem. 61 1989 613 628
12. C.W. Tornøe, C. Christensen, and M.J. Meldal J. Org. Chem. 67 2002 3057 3064
13. V.V. Rostovtsev, L.G. Green, V.V. Fokin, and K.B. Sharpless Angew. Chem. Int. Ed. 41 2002 2596 2599
14. M. Meldal, and C.W. Tornøe Chem. Rev. 108 2008 2952 3015
15. D. Astruc Nanoparticles and Catalysis 2008 Wiley-VCH Verlag GmbH & Co, KGaA Weinheim chapter 1
16. J. Zhang, Y. Wang, H. Ji, Y. Wei, N. Wu, B. Zuo, and Q. Wang J. Catal. 229 2005 114 118
17. H.M.R. Gardimalla, D. Mandal, P.D. Stevens, M. Yen, and Y. Gao Chem. Commun. 2005 4432 4434
18. P.D. Stevens, G. Li, J. Fan, M. Yen, and Y. Gao Chem. Commun. 2005 4435 4437
19. J. Lee, D. Lee, E. Oh, J. Kim, Y.-P. Kim, S. Jin, H.-S. Kim, Y. Hwang, J.H. Kwak, J.-G. Park, C.-H. Shin, J. Kim, and T. Hyeon Angew. Chem. Int. Ed. 44 2005 7427 7432
20. T.-J. Yoon, J.S. Kim, B.G. Kim, K.N. Yu, M.-H. Cho, and J.-K. Lee Angew. Chem. Int. Ed. 44 2005 1068 1071
21. U. Laska, C.G. Frost, G.J. Price, and P.K. Plucinski J. Catal. 268 2009 318 328
22. A.K. Gupta, and M. Gupta Biomaterials 26 2005 3995 4021
23. B.C. Zhu, and X.Z. Jiang Appl. Organomet. Chem. 21 2007 345 349
24. P. Kuhn, A. Alix, M. Kumarraja, B. Louis, P. Pale, and J. Sommer Eur. J. Org. Chem. 2009 423 429
25. T. Oishi, T. Katayama, K. Yamaguchi, and N. Mizuno Chem. Eur. J. 15 2009 7539 7542
26. C. Wei, Z. Li, and C.-J. Li Synlett 2004 1472 1483
27. C.-J. Li Acc. Chem. Res. 43 2010 581 590
28. W.J. Yoo, L. Zhao, and C.-J. Li Aldrichima Acta 44 2011 43 51
29. M.J. Aliaga, D.J. Ramón, and M. Yus Org. Biomol. Chem. 8 2010 43 46
30. M. Laksmi Kantam, V. Swarna Jaya, B. Sreedhar, M. Mohan Rao, and B.M. Choudary J. Mol. Catal. A Chem. 256 2006 273 277
31. H. Sharghi, M.H. Beyzavi, A. Safavi, M.M. Doroodmand, and R. Khalifeh Adv. Synth. Catal. 351 2009 2391 2410
32. H. Sharghi, R. Khalifeh, and M.M. Doroodmand Adv. Synth. Catal. 351 2009 207 218
33. V. Bénéteau, A. Olmos, T. Boningari, J. Sommer, and P. Pale Tetrahedron Lett. 51 2010 3673 3677
34. F. Alonso, C. Vitale, G. Radivoy, and M. Yus Synthesis 2003 443 447
35. F. Alonso, Y. Moglie, G. Radivoy, C. Vitale, and M. Yus Appl. Catal. A Gen. 271 2004 171 176
36. G. Radivoy, F. Alonso, Y. Moglie, C. Vitale, and M. Yus Tetrahedron 61 2005 3859 3864
37. F. Nador, L. Fortunato, Y. Moglie, C. Vitale, and G. Radivoy Synthesis 2009 4027 4031
38. F. Alonso, Y. Moglie, G. Radivoy, and M. Yus Tetrahedron Lett. 50 2009 2358 2362
39. F. Alonso, Y. Moglie, G. Radivoy, and M. Yus Eur. J. Org. Chem. 2010 1875 1884
40. F. Alonso, Y. Moglie, G. Radivoy, and M. Yus Adv. Synth. Catal. 352 2010 3208 3214
41. F. Alonso, Y. Moglie, G. Radivoy, and M. Yus Org. Biomol. Chem. 9 2011 6385 6395
42. F. Alonso, Y. Moglie, G. Radivoy, and M. Yus J. Org. Chem. 76 2011 8394 8405
43. F. Alonso, Y. Moglie, G. Radivoy, and M. Yus Heterocycles 84 2012 1033 1044
44. M.J. Albaladejo, F. Alonso, Y. Moglie, and M. Yus Eur. J. Org. Chem. 2012 3093 3104
45. F. Alonso, T. Melkonian, Y. Moglie, and M. Yus Eur. J. Org. Chem. 2011 2524 2530
46. D.D. Perrin, and W.L.F. Amarego Purification of Laboratory Chemicals 1988 Pergamon Press Oxford
47. J. Jung, S. Bae, and W. Lee Appl. Catal. B 127 2012 148 158
48. J.J. Scholten, A.P. Pijpers, and M.L. Hustings Catal. Rev. Sci. Eng. 27 1985 151 206
49. Th.J. Osinga, B.G. Linsen, and W.P. van Beet J. Catal. 7 1967 227 279
50. L. Brandsma, H.D. Verkruijsse, and B. Walda Synth. Commun. 21 1991 137 139
51. For a review, see: L.D. Pachón, and G. Rothenberg Appl. Organomet. Chem. 22 2008 288 299