Copper-alginates: A biopolymer supported Cu(II) catalyst for 1,3-dipolar cycloaddition of alkynes with azides and oxidative coupling of 2-naphthols and phenols in water

Catalysis Letters

Volumn 114, Issue 1-2, 2007, Pages 36-40

  Reddy, K Rajender ^a   Rajgopal, K ^a   Kantam, M Lakshmi ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

Alginate; Alkynes; Azides; Biopolymer; Copper(II) catalyst; Cycloaddition; Oxidative coupling; Phenols

Indexed keywords

BIOPOLYMERS; COPPER; CYCLOADDITION; FILTRATION; PHENOLS;

ALGINATE; ALKYNES; AZIDES; COPPER(II) CATALYST; OXIDATIVE COUPLING;

SALTS;

EID: 34247609879     PISSN: 1011372X     EISSN: 1572879X     Source Type: Journal    
DOI: 10.1007/s10562-007-9032-x     Document Type: Article

References (28)

1. R.A. Sheldon and H. van Bekkum, Fine Chemicals through Heterogeneous Catalysis (Wiley-VCH, Weinheim, 2001).
2. A. Kirschning, Immobilized Catalysis: Solid Phases, Immobilization and Applications (Springer, Berlin, 2004).
3. J.H. Clark and D.J. Macquarrie, Green Chemistry and Technology (Blackwell, Abingdon, 2002).
4. E. Guibal, Prog. Polym. Sci. 30 (2005) 71.
5. F. Quignard and A. Choplin, Chem. Commun. (2001) 21.
6. X. Zhang, Y. Geng, B. Han, M.-Y. Ying, M.-Y. Huang and Y.Y. Jiang, Polym. Adv. Technol. 12 (2001) 642.
7. K. Huang, L. Xue, Y.-C. Hu, M.-Y. Huang and Y.-Y. Jiang, React. Funct. Polym. 50 (2002) 199.
8. (a) D.J. Macquarrie and J.J. E. Hardy, Ind. End. Chem. Res. 44 (2005) 8499;
9. (b) F. Quignard, A. Choplin and A. Domard, Langmuir 16 (2000) 9106;
10. (c) L.F. Xiao, F.W. Li and C.G. Xia, Applied. Catal. A: 279 (2005) 125;
11. (d) K. Rajender Reddy, K. Rajgopal, C. Uma Maheswari and M. Lakshmi Kantam, New. J. Chem. 30 (2006) 1549.
12. P. Stanford and J. Baird, in: The polysaccharides, Vol. 2, (Academic Press, New York, 1983) 411.
13. A. Martinsen, G. Skjak-Braek and O. Smidsrod, Biotechnol. Bioeng. 33 (1989) 79.
14. W.R. Gombotz and S.F. Wee, Adv. Drug. Delivery. Rev. 31 (1998) 267.
15. (a) A.I. Zouboulis and I.A. Katsoyiannis, Ind. Eng. Chem. Res. 41 (2002) 6149;
16. (b) A.K. Pandey, S.D. Pandy, V. Misra and S. Dcvi, J. Hazardous. Materials. B 98 (2003) 177;
17. (c) H. Mimura, H. Ohta, K. Akiba and Y. Onodera, J. Nucl. Sci. Technol. 39 (2002) 655.
18. K. Rajender Reddy, N.S. Kumar, P.S. Reddy, B. Sreedhar and M. Lakshmi Kantam, J. Mol. Catal. A 252 (2006) 12.
19. K. Rajender Reddy, N.S. Kumar, B. Sreedhar and M. Lakshmi Kantam, J. Mol. Catal. A 252 (2006) 136.
20. K. Rajender Reddy, and N.S. Kumar, Synlett (2006) 2246.
21. Z. Aksu, G. Egretli and T. Kutsel, Process Biochem. 33 (1998) 393.
22. V.V. Rostovtsev, L.G. Green, V.V. Fokin and K.B. Sharpless, Angew. Chem. Int. Ed. 41 (2002) 2596.
23. K. Rajender Reddy, K. Rajgopal, and M. Lakshmi Kantam, Synlett (2006) 957.
24. G. Bringmann and R. Walter, Angew. Chem. Int. Ed. Engl. 29 (1990) 977.
25. E. Armengol, A. Corma, H. Garcia, and J. Primo, Eur. J. Org. Chem. (1999) 1915.
26. M. Lakshmi Kantam, B. Kavita and F. Figueras, Catal. Lett. 51 (1998) 113.
27. P. Mastrorilli, F. Muscio, G.P. Suranna, C.F. Nobile and M. Latronico, J. Mol. Catal. A 165 (2001) 81.
28. M. Matsushita, K. Kamata, K. Yamaguchi and N. Mizuno, J. Am. Chem. Soc. 127 (2005) 6632.