Nano-copper catalyzed three-component reaction to construct 1,4-substituted 1,2,3-triazoles

Tetrahedron Letters

Volumn 55, Issue 14, 2014, Pages 2312-2316

  Huang, Lina ^a   Liu, Wei ^a   Wu, Juncheng ^a   Fu, Ying ^a   Wang, Kehu ^a   Huo, Congde ^a   Du, Zhengyin ^a  

^a NORTHWEST NORMAL UNIVERSITY   (China)

Author keywords

Click chemistry; Copper nanoparticles; Cycloaddition; Multicomponent reaction; Phenylacetylene

Indexed keywords

1,2,3 TRIAZOLE DERIVATIVE; ALKYNE; COPPER NANOPARTICLE; HALIDE; SODIUM AZIDE;

ARTICLE; CATALYSIS; CATALYST; CYCLOADDITION; PARTICLE SIZE; SUBSTITUTION REACTION; SURFACE PROPERTY;

EID: 84897458713     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2014.02.114     Document Type: Article

References (36)

1. B.S.P. Anil Kumar, K.H.V. Reddy, B. Madhav, K. Ramesh, and Y.V.D. Nageswar Tetrahedron Lett. 53 2012 4595 4599
2. R. Breslow Acc. Chem. Res. 24 1991 159 164
3. R. Breslow Acc. Chem. Res. 37 2004 471 478
4. M. Meldal, and C.W. Tornøe Chem. Rev. 108 2008 2952 3015
5. I.P. Beletskaya, and A.V. Cheprakov Coord. Chem. Rev. 248 2004 2337 2364
6. V.V. Fokin ACS Chem. Biol. 2 2007 775 778
7. B.H. Lipshutz, and Y. Yamamoto Chem. Rev. 108 2008 2793 2795
8. B.C. Ranu, R. Dey, T. Chatterjee, and S. Ahammed ChemSusChem 5 2012 22 44
9. P. Appukkuttan, V.P. Mehta, and E.V.V. Der Eycken Chem. Soc. Rev. 39 2010 1467 1477
10. J.E. Moses, and A.D. Moorhouse Chem. Soc. Rev. 36 2007 1249 1262
11. J.F. Lutz Angew. Chem., Int. Ed. 46 2007 1018 1025
12. Q.A. Pankhurst, J. Jones, and S.K. Connolly Appl. Phys. 36 2003 167 181
13. J.M. Perez, F.J. Simeone, Y. Saeki, L. Josephson, and R. Weissleder J. Am. Chem. Soc. 125 2003 10192 10193
14. B. Kaboudin, Y. Abedi, and T. Yokomatsu Org. Biomol. Chem. 10 2012 4543 4548
15. M. Takahashi, and D. Suga Synthesis 7 1998 986 990
16. J. Das, S.N. Patil, R. Awasthi, C.P. Narasimhulu, and S. Trehan Synthesis 2005 1801 1806
17. J. Gavenois, and T.D. Tilley Organometallics 21 2002 5549 5563
18. J. Gavenonis, and T.D. Tilley J. Am. Chem. Soc. 124 2002 8536 8537
19. E.D. Goddard-Borger, and R.V. Stick Org. Lett. 9 2007 3797 3800
20. C.Z. Tao, X. Cui, J. Li, A.X. Liu, L. Liu, and Q.X. Guo Tetrahedron Lett. 48 2007 3525 3529
21. Q. Liu, and Y. Tor Org. Lett. 5 2003 2571 2572
22. Y. Li, L.X. Gao, and F.S. Han Chem. Eur. J. 16 2010 7969 7972
23. H. Yang, Y. Li, M. Jiang, J. Wang, and H. Fu Chem. Eur. J. 17 2011 5652 5660
24. F. Alonso, Y. Moglie, G. Radivoy, and M. Yus Synlett 2012 2179 2182
25. G.A. Molander, and J. Ham Org. Lett. 13 2006 2767 2770
26. F. Ilgen, and B. Konig Green Chem. 11 2009 848 854
27. N. Mukherjee, S. Ahammed, S. Bhadra, and B.C. Ranu Green Chem. 15 2013 389 397
28. B. Kaboudin, Y. Abedi, and T. Yokomatsub Org. Biomol. Chem. 10 2012 4543 4548
29. A.K. Feldman, B. Colasson, and V.V. Fokin Org. Lett. 22 2004 3897 3899
30. S. Lal, and S. Díez-Gonzalez J. Org. Chem. 76 2011 2367 2373
31. Y.M.A. Yamada, S.M. Sarkar, and Y. Uozumi J. Am. Chem. Soc. 134 2012 9285 9290
32. K. Szabolcs, K. Zih-Perényi, R. Ádám, and N. Zoltán Synthesis 24 2012 3722 3730
33. P. Veerakumar, M. Velayudham, K.L. Lub, and S. Rajagopal Catal. Sci. Technol. 1 2011 1512
34. H. Sharghi, R. Khalifeh, and M.M. Doroodmand Adv. Synth. Catal. 351 2009 207 218
35. P. Abdulkin, Y. Moglie, B.R. Knappett, D.A. Jefferson, M. Yus, F. Alonso, and A.E.H. Wheatley Nanoscale 5 2013 342 350
36. L.D. Pachon, J.H. van Maarseveen, and G. Rothenberg Adv. Synth. Catal. 347 2005 811 815