Copper(I) and palladium nanoparticles supported on ethylenediamine- functionalized cellulose as an efficient catalyst for the 1,3-dipolar cycloaddition/direct arylation sequence

Applied Organometallic Chemistry

Volumn 28, Issue 2, 2014, Pages 116-119

  Keshipour, Sajjad ^a   Shaabani, Ahmad ^a  

^a SHAHID BEHESHTI UNIVERSITY   (Iran)

Author keywords

1,3 dipolar cycloaddition; arylation; cellulose; heterogeneous catalyst

Indexed keywords

1 ,2 ,3-TRIAZOLES; 1 ,3-DIPOLARCYCLOADDITION; ARYLATIONS; BIO-SUPPORTED CATALYST; EFFICIENT CATALYSTS; ETHYLENE DIAMINE; HETEROGENEOUS CATALYST; PALLADIUM NANOPARTICLES;

AROMATIC COMPOUNDS; CELLULOSE; CYCLOADDITION; NANOPARTICLES; SYNTHESIS (CHEMICAL);

CATALYSTS;

EID: 84893699681     PISSN: 02682605     EISSN: 10990739     Source Type: Journal    
DOI: 10.1002/aoc.3091     Document Type: Article

References (20)

1. M. J. Gronnow, R. J. White, J. H. Clark, D. J. Macquarrie, Org. Process Res. Dev. 2005, 9, 516-518.
2. A. Barau, R. Luque, V. Budarin, A. Prelle, V. S. Teodorescu, A. Caragheorgheopol, D. J. Macquarrie, M. Zaharescu, in 14th International Sol-Gel Conference, Montpellier, France, Book of Abstracts, 2007, p. 604.
3. W. C. Ketchie, M. Murayama, R. J. Davis, J. Catal. 2007, 250, 264-273.
4. P. Raveendran, J. Fu, S. L. Wallen, Green Chem. 2006, 8, 34-38.
5. M. F. Lengke, M. E. Fleet, G. Southam, Langmuir 2007, 23, 8982-8987.
6. D. Klemm, B. Heublein, H. P. Fink, A. Bohn, Angew. Chem. Int. Ed. 2005, 44, 3358-3393.
7. K. R. Reddy, N. S. Kumar, P. S. Reddy, B. Sreedhar, M. L. Kantam, J. Mol. Catal. A: Chem. 2006, 252, 12-16.
8. C. M. Cirtiu, A. F. Dunlop-Brière, A. Moores, Green Chem. 2011, 13, 288-291.
9. V. V. Rostovtsev, L. G. Green, V. V. Fokin, K. B. Sharpless, Angew. Chem. Int. Ed. 2002, 41, 2596-2599.
10. M. S. Costa, N. Boechat, E. A. Rangel, F. D. Da Silva, A. M. T. de Souza, C. R. Rodrigues, H. C. Castro, I. N. Junior, M. C. S. Lourenco, S. Wardell, V. F. Ferreira, Bioorg. Med. Chem. 2006, 14, 8644-8653.
11. H. Nandivada, X. W. Jiang, J. Lahann, Adv. Mater. 2007, 19, 2197-2208.
12. G. C. Tron, T. Pirali, R. A. Billington, P. L. Canonico, G. Sorba, A. A. Genazzani, Med. Res. Rev. 2008, 28, 278-308.
13. S. Chuprakov, N. Chernyak, A. S. Dudnik, V. Gevorgyan, Org. Lett. 2007, 9, 2333-2336.
14. L. Ackermann, H. K. Potukuchi, D. Landsberg, R. Vicente, Org. Lett. 2008, 10, 3081-3084.
15. B. C. Boren, S. Narayan, L. K. Rasmussen, L. Zhang, H. Zhao, Z. Lin, G. Jia, V. V. Fokin, J. Am. Chem. Soc. 2008, 130, 8923-8930.
16. B. Liégault, D. Lapointe, L. Caron, A. Vlassova, K. Fagnou, J. Org. Chem. 2009, 74, 1826-1834.
17. L. Ackermann, R. Vicente, Org. Lett. 2009, 11, 4922-4925.
18. H. C. Kolb, M. G. Finn, K. B. Sharpless, Angew. Chem. Int. Ed. 2001, 40, 2004-2021.
19. S. Keshipour, S. Shojaei, A. Shaabani, Cellulose 2013, 20, 973-980.
20. J. J. Verendel, T. L. Church, P. G. Andersson, Synthesis 2011, 1649-1677.