Mesoporous nickel hydroxyapatite nanocomposite for microwave-assisted Henry reaction

Tetrahedron Letters

Volumn 53, Issue 24, 2012, Pages 2980-2984

  Neelakandeswari, N ^a   Sangami, G ^a   Emayavaramban, P ^a   Karvembu, R ^b   Dharmaraj, N ^a   Kim, Hak Yong ^c  

^a BHARATHIAR UNIVERSITY   (India)

^b NATIONAL INSTITUTE OF TECHNOLOGY   (India)

^c Chonbuk National University   (South Korea)

Author keywords

Green chemistry; Henry reaction; Heterogeneous catalysis; Nickel hydroxyapatite

Indexed keywords

ALDEHYDE; AROMATIC COMPOUND; HYDROXYAPATITE; NANOCOMPOSITE; NICKEL; NITROMETHANE; SOLVENT;

ARTICLE; CATALYST; CHEMICAL REACTION; CHEMICAL STRUCTURE; GAS CHROMATOGRAPHY; HENRY REACTION; MICROWAVE RADIATION; NUCLEAR MAGNETIC RESONANCE; SCANNING ELECTRON MICROSCOPY; TRANSMISSION ELECTRON MICROSCOPY;

EID: 84861198851     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2012.03.086     Document Type: Article

References (29)

1. K. Mori, T. Hara, T. Mizugaki, K. Ebitani, and K. Kaneda J. Am. Chem. Soc. 126 2004 10657 10666
2. S. Wuyts, D.E. De Vos, F. Verpoort, D. Depla, R. De Gryse, and P.A. Jacobs J. Catal. 219 2003 417 424
3. M. Murata, T. Hara, K. Mori, M. Ooe, T. Mizugaki, K. Ebitani, and K. Kaneda Tetrahedron Lett. 44 2003 4981 4984
4. R. Tahir, K. Banert, A. Solhy, and S. Sebti J. Mol. Catal. A: Chem. 246 2006 39 42
5. K. Wang, G.J. Kennedy, and R.A. Cook J. Mol. Catal. A: Chem. 298 2009 88 93
6. B.M. Choudary, C. Sridhar, M.L. Kantam, G.T. Venkanna, and B. Sreedhar J. Am. Chem. Soc. 127 2005 9948 9949
7. B.M. Choudary, C. Sridhar, M.L. Kantam, and B. Sreedhar Tetrahedron Lett. 45 2004 7319 7321
8. K. Yasukazu, H. Junpei, K. Seishiro, Y. Yuichiro, O. Kohji, N. Daisuke, K. Mikio, and Y. Muneyoshi Appl. Catal. A: Chem. 395 2011 129 137
9. T. Okino, S. Nakamura, T. Furukawa, and Y. Takemoto Org. Lett. 6 2004 625 627
10. D.A. Evans, D. Seidel, M. Rueping, H.W. Lam, J.T. Shaw, and C.W. Downey J. Am. Chem. Soc. 125 2003 12692 12693
11. R. Ballini, G. Bosica, and P. Forconi Tetrahedron 52 1996 1677 1684
12. A. Cwik, A. Fuchs, Z. Hell, and J.M. Clacens Tetrahedron 61 2005 4015 4021
13. Y. Xi, and R.J. Davis J. Mol. Catal. A: Chem. 341 2011 22 27
14. B.M. Choudary, M.L. Kantam, and B. Kavita J. Mol. Catal. A: Chem. 169 2001 193 197
15. Y. Sugi, K. Komura, and T. Kawamura Cat. Commun. 8 2007 644 648
16. R. Ballini, G. Bosica, D. Livi, A. Palmieri, R. Maggi, and G. Sartori Tetrahedron Lett. 44 2003 2271 2273
17. J. McNulty, J.A. Steere, and S. Wolf Tetrahedron Lett. 39 1998 8013 8016
18. R.S. Varma, R. Dahiya, and S. Kumar Tetrahedron Lett. 38 1997 5131 5134
19. P. Lidström, J. Tierney, B. Wathey, and J. Westman Tetrahedron 57 2001 9225 9283
20. A. Lew, P.O. Krutzik, M.E. Hart, and A.R. Chamberlin J. Comb. Chem. 4 2001 95 105
21. B. Wathey, J. Tierney, P. Lidström, and J. Westman Drug Discovery Today 7 2002 373 380
22. R.S. Varma Green Chem. 1 1999 43 55
23. S. Delvin Green Chemistry 1st ed. 2006 IVY Publishing House New Delhi
24. R. Xu, J. Zhang, Y. Tian, and J. Zhou J. Iran. Chem. Soc. 6 2009 443 447
25. Z. Boukha, M. Kacimi, M.F.R. Pereira, J.L. Faria, J.L. Figueiredo, and M. Ziyad Appl. Catal. A: Gen. 317 2007 299 309
26. S. Brunauer, L.S. Deming, W.S. Deming, and E. Teller J. Am. Chem. Soc. 62 1940 1723
27. M.J. Zhi, X.Q. Chen, H. Finklea, I. Celik, and N.Q.Q. Wu J. Power Sources 183 2008 485 490
28. G. Jose Santamaria, L. Maria Martinez, and A. Lopez J. Chem. Soc., Faraday Trans. 93 1997 493 497
29. A. Loupy, L. Perreux, M. Liagre, K. Burle, and M. Moneuse Pure Appl. Chem. 73 2001 161 166