Novel basic mesoporous catalysts for the Friedländer reaction from 2-Aminoaryl ketones: Quinolin-2(1H)-ones versus quinolines

ChemCatChem

Volumn 1, Issue 2, 2009, Pages 241-243

  Domínguez Fernández, Fernando ^a   López Sanz, Jesús ^a   Pérez Mayoral, Elena ^a   Bek, David ^b   Martín Aranda, Rosa M ^a   López Peinado, Antonio J ^a   Čejka, Jiri ^b  

^a UNIVERSIDAD NACIONAL DE EDUCACIÓN A DISTANCIA   (Spain)

^b J HEYROVSKÝ INSTITUTE OF PHYSICAL CHEMISTRY   (Czech Republic)

Author keywords

Basicity; Heterogeneous catalysis; Ketones; Mesoporous materials; Quinolines

Indexed keywords

ACID/BASE PROPERTIES; EFFICIENT CATALYSTS; ETHYLACETOACETATE; MESOPOROUS CATALYSTS; QUINOLINES;

ALKALINITY; CATALYSIS; CATALYSTS; MESOPOROUS MATERIALS; MOLECULAR SIEVES;

KETONES;

EID: 77952986646     PISSN: 18673880     EISSN: 18673899     Source Type: Journal    
DOI: 10.1002/cctc.200900097     Document Type: Article

References (26)

1. V. Kouznetsov, L. Y. V. Móndez, C. M. M. Gómez, Curr. Org. Chem. 2005, 9, 141-161.
2. J. P. Michael, Nat. Prod. Rep. 2002, 19, 742-746.
3. G. R. Newkome, W. W. Paudler in Contemporary Heterocyclic Chemistry, Wiley, New York, 1982, pp. 199-231.
4. A. R. Katritzky, Handbook of Heterocyclic Chemistry, Pergamon Press, Oxford, 1985.
5. a) C.-C. Cheng, S.-J. Yan, Org. React. 1982, 28, 37-201;
6. b) J. Marco- Contelles, E. Pérez-Mayoral, A. Samadi, M. C. Carreiras, E. Soriano, Chem. Rev. 2009, 109, 2652-2671.
7. J. M. Muchowski, M. L. Maddox, Can. J. Chem. 2004, 82, 461-478.
8. K. Mogilaiah, K. Vidya, Indian J. Chem., Sect. B 2007, 46B, 1721-1723.
9. a) A. Shaabani, E. Soleimani, Z. Badri, Monatsh. Chem. 2006, 137, 181- 184;
10. b) M. A. Zolfigol, P. Salehi, M. Shiri, T. F. Rastegar, A. Ghaderi, J. Iran. Chem. Soc. 2008, 5, 490-497;
11. c) B. Das, K. Damodar, N. Chowdhury, R. A. Kumar, J. Mol. Catal. A: Chem. 2007, 274, 148-152.
12. a) M. Dabiri, S. C. Azimi, A. Bazgir, Monatsh. Chem. 2007, 138, 659-661;
13. b) U. V. Desai, S. D. Mitragotri, T. S. Thopate, D. M. Pore, P. P. Wadgaonkar, Arkivoc 2006, 198-204.
14. M. Narasimhulu, T. S. Reddy, K. C. Mahesh, P. Prabhakar, Ch. B. Rao, Y. Venkateswarlu, J. Mol. Catal. A: Chem. 2007, 266, 114-117.
15. B. Das, M. Krishnaiah, K. Laxminarayana, D. Nandankumar, Chem. Pharm. Bull. 2008, 56, 1049-1051.
16. A. A. Mohammadi, J. Azizian, A. Hadadzahmatkesh, M. R. Asghariganjeh, Heterocycles 2008, 75, 947-954.
17. A. Shaabani, A. Rahmati, Z. Badri, Catal. Commun. 2008, 9, 13-16.
18. E. A. Fehnel, J. Heterocycl. Chem. 1967, 4, 565-570.
19. E. Pérez-Mayoral, R. M. Martí n-Aranda, A. J. Lo ́ pez-Peinado, P. Ballesteros, A. Zukal, J. Čejka, Top. Catal. 2009, 52, 148-152.
20. C.-S. Jia, Y.-W. Dong, S.-J. Tu, G.-W Wang, Tetrahedron 2007, 63, 892-897.
21. a) Y. Kobayashi, T. Harayama, Org. Lett. 2009, 11, 1603-1606;
22. b) P. Hewawasam, W. Fan, M. Ding, K. Flint, D. Cook, G. D. Goggins, R. A. Myers, V. K. Gribkoff, C. G. Boissard, S. I. Dworetzky, J. E. Starrett, Jr., N. J. Lodge, J. Med. Chem. 2003, 46, 2819-2822;
23. c)W. W. K. R. Mederski, M. Osswald, D. Dorsch, M. Christadler, C.-J. Schmitges, C. Wilm, Bioorg. Med. Chem. Lett. 1997, 7, 1883-1886.
24. H. Balcar, J. Čejka, J. Sedlaček, J. Svoboda, J. Zednik, Z. Bastl, V. Bosáček, J. Vohlidal, J. Mol. Catal. A: Chem. 2003, 203, 287-298.
25. a) D. Zhao, Q. Huo, J. Feng, B. F. Chmelka, G. D. Stucky, J. Am. Chem. Soc. 1998, 120, 6024-6036;
26. b) A. Zukal, H. Šiklová, J. Čejka, Langmuir 2008, 24, 9837-9842.