Cellulose sulfuric acid catalyzed multicomponent reaction for efficient synthesis of 1,4-dihydropyridines via unsymmetrical Hantzsch reaction in aqueous media

Journal of Molecular Catalysis A: Chemical

Volumn 335, Issue 1-2, 2011, Pages 46-50

  Safari, Javad ^a   Banitaba, Sayed Hossein ^a   Khalili, Shiva D ^a  

^a UNIVERSITY OF KASHAN   (Iran)

Author keywords

Aqueous media; Biodegradable catalysts; Cellulose sulfuric acid; Hantzsch reaction; One step condensation

Indexed keywords

AQUEOUS MEDIA; BIODEGRADABLE CATALYSTS; CELLULOSE SULFURIC ACID; HANTZSCH REACTIONS; ONE-STEP CONDENSATION;

CATALYSTS; CELLULOSE; CONDENSATION; SYNTHESIS (CHEMICAL);

SULFURIC ACID;

EID: 78751643283     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2010.11.012     Document Type: Article

References (34)

1. A. Domling, and I. Ugi Angew. Chem. Int. Ed. 39 2000 3168 3173
2. J. Zhu, and H. Bienayme Multi Component Reactions 2005 Wiley-VCH Weinheim
3. A. Domling Chem. Rev. 106 2006 17 23
4. I. Ugi Pure Appl. Chem. 73 2001 187 191
5. R.R. Nagawade, and D.B. Shinde Acta Chim. Slov. 54 2007 642 645
6. D.M. D'Souza, and T.J. Mueller Chem. Soc. Rev. 36 2007 3169 3173
7. C.C.A. Cariou, G.J. Clarkson, and M. Shipman J. Org. Chem. 73 2008 9762 9764
8. C. Kalinski, H. Lemoine, J. Schmidt, C. Burdack, J. Kolb, M. Umkehrer, and G. Ross Synlett 2008 4007 4011
9. G.M. Reddy, M. Shiradkar, and A.K. Chakravarthy Curr. Org. Chem. 11 2007 484 487
10. R.A. Janis, and D.A. Triggle J. Med. Chem. 25 1983 775 779
11. R.H. Bocker, and F.P. Guengerich J. Med. Chem. 28 1986 1596 1601
12. A.C. Gaudio, A. Korolkovas, and Y. Tkahata J. Pharm. Sci. 83 1994 1110 1114
13. M.F. Gordeev, D.V. Patel, and E.M. Gordon J. Org. Chem. 61 1996 924 927
14. A. Dondoni, A. Massi, E. Minghini, and V. Bertolasi Tetrahedron 60 2004 2311 2314
15. A. Hantzsch Ber. Dtsch. Chem. Ges. 14 1881 1637 1640
16. B. Love, and K.M. Sander J. Org. Chem. 30 1965 1914 1919
17. G.V.M. Sharma, K.L. Reddy, P.S. Lakshmi, and P.R. Krishna Synthesis 2006 55 58
18. T. Itoh, K. Nagata, M. Miyazaki, H. Ishikawa, A. Kurihara, and A. Ohsawa Tetrahedron 60 2004 6649 6655
19. R. Ruppert, C. Jeandon, A. Sgambati, and H. Callot Chem. Commun. 1999 2123 2124
20. S. Ko, and C.F. Yao Tetrahedron Lett. 62 2006 7293 7299
21. A. Kumar, and R.A. Maurya Synlett 6 2008 883 885
22. A. Debache, R. Boulcina, A. Belfaitah, S. Rhouati, and B. Carboni Synlett 2008 509 512
23. A. Agarwal, and P.M.S. Chauhan Tetrahedron Lett. 46 2005 1345 1348
24. R. Sridhar, and P.T. Perumal Tetrahedron 61 2005 2465 2469
25. K. Shengkai, and Y. Ching-Fa Tetrahedron 62 2006 7293 7299
26. N. Tewari, N. Dwivedi, and R.P. Tripathi Tetrahedron Lett. 45 2004 9011 9014
27. S. Ko, M.N.V. Sastry, C. Lin, and C.F. Yao Tetrahedron Lett. 46 2005 5771 5774
28. L.M. Wang, J. Sheng, L. Zhang, J.W. Han, Z. Fan, H. Tian, and C.T. Qian Tetrahedron 61 2005 1539 1543
29. R. Breslow Acc. Chem. Res. 13 1980 170 174
30. J.H. Clark, and D.J. Macquarrie Green Chemistry and Technology 2002 Blackwell Abingdon
31. S. Ahmad, and M. Ali Appl. Catal. A: Gen. 331 2007 149 153
32. S. Ahmad, M. Ali, R. Jafar, and S. Ebrahim Chem. Pharm. Bull. 55 6 2007 957 961
33. J. Venu Madhav, Y. thirupathi Reddy, and P. Narsimha Reddy J. Mol. Catal. A: Chem. 304 2009 85 87
34. S. Ahmad, R. Abbas, and B. Zahra Catal. Commun. 9 2009 13 15