Cobalt nanoparticles promoted highly efficient one pot four-component synthesis of 1, 4-dihydropyridines under solvent-free conditions

Cuihua Xuebao/Chinese Journal of Catalysis

Volumn 32, Issue 12, 2011, Pages 1850-1855

  Safari, Javad ^a   Banitaba, Sayed Hossein ^a   Dehghan Khalili, Shiva ^a,b  

^a UNIVERSITY OF KASHAN   (Iran)

^b ISLAMIC AZAD UNIVERSITY   (Iran)

Author keywords

1, 4 dihydropyridine; Cobalt nanoparticle; Four component condensation; Heterogeneou catalyst; Magnetically separable catalyst

Indexed keywords

EID: 84856380241     PISSN: 02539837     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (40)

1. Safari J, Khalili S D, Rezaei M, Banitaba S H, Meshkani F. Monatsh Chem, 2010, 141: 1339.
2. Peng Q, Yang Y, Yuan Y. J Mol Catal A, 2004, 219: 175.
3. Fu H, Li M, Chen H, Li X. J Mol Catal A, 2006, 259: 156.
4. Paulik F E. Catal Rev, 1972, 6: 49.
5. Beller M, Cornils B, Frohning C D, Kohlpaintner C W. J Mol Catal A, 1995, 104: 17.
6. Ungvary F. Coord Chem Rev, 2007, 251: 2087.
7. Wen F, BO̧nnemann H, Jiang J, Lu D, Wang Y, Jin Z. Appl Organomet Chem, 2005, 19: 81.
8. Bruss A J, Gelesky M A, Machado G, Dupont J. J Mol Catal A, 2006, 252: 212.
9. Ma L, Peng Q, He D. Catal Lett, 2009, 130: 137.
10. Anastas P T, Warner J C. In: Green Chemistry: Theory and Practice. Oxford: Oxford University Press, 1998.
11. Kalinski C, Lemoine H, Schmidt J, Burdack C, Kolb J, Umkehrer M, Ross G. Synlett, 2008: 4007.
12. Debache A, Ghalem W, Boulcina R, Belfaitah A, Rhouati S, Carboni B. Tetrahedron Lett, 2009, 50: 5248.
13. Klusa V. Drugs Future, 1995, 20: 135.
14. Bretzel R G, Bollen C C, Maeser E, Federlin K F. Am J Kidney Dis, 1993, 21(6s3): 53.
15. Bretzel R G, Bollen C C, Maeser E, Federlin K F. Drugs Future, 1992, 17: 465.
16. Rainer B, Volker G. Drugs Future, 1995, 20: 499.
17. Janis R A, Triggle D J. J Med Chem, 1983, 26: 775.
18. Boecker R H, Guengerich F P. J Med Chem, 1986, 29: 1596.
19. Gaudio A C, Korolkovas A, Tkahata Y. J Pharm Sci, 1994, 83: 1110.
20. Gordeev M F, Patel D V, Gordon E M. J Org Chem, 1996, 61: 924.
21. Svetlik J, Veizerova L, Kittmann V. Tetrahedron Lett, 2008, 49: 3520.
22. Suzuki I, Suzumura Y, Takeda K. Tetrahedron Lett, 2006, 47: 7861.
23. Shaabani A, Bazgir A, Teimouri F. Tetrahedron Lett, 2003, 44: 857.
24. Li M, Zuo Z, Wen L, Wang S. J Comb Chem, 2008, 10: 436.
25. Sabitha G, Reddy G S K, Reddy C S, Yadav J S. Tetrahedron Lett, 2003, 44: 4129.
26. Heravi M M, Bakhtiri K, Javadi N M, Bamoharram F F, Saeedi M, Oskooi H A. J Mol Catal A, 2007, 264: 50.
27. Cherkupally S R, Mekalan R. Chem Pharm Bull, 2008, 56: 1002.
28. Wang L M, Sheng J, Zhang L, Han J W, Fan Z Y, Tian H, Qian C T. Tetrahedron, 2005, 61: 1539.
29. Ji S, Jiang Z Q, Lu J, Loh T P. Synlett, 2004: 831.
30. Sainani J B, Shah A C, Arya V P. Indian J Chem Sect B, 1994, 33B: 526.
31. Kumar A, Maurya R A. Tetrahedron Lett, 2007, 48: 3887.
32. Ko S, Yao C F. Tetrahedron, 2006, 62: 7293.
33. Tu S J, Yan S, Cao X D, Wu S S, Zhang X H, Hao W J, Han Z G, Shi F J. Organomet Chem, 2009, 649: 91.
34. Zang H, Zhang Y, Zang Y, Cheng B-W. Ultrason Sonochem, 2010, 17: 495.
35. Tu S J, Zhou J F, Deng X, Cai P J, Wang H, Feng J C. Chin J Org Chem, 2001, 21: 313.
36. Wang X S, Shi D Q, Tu S J. Synth Commun, 2002, 32: 3449.
37. Chen W Y, Lu J, Jin J R. Lett Org Chem, 2006, 3: 317.
38. Kim S W, Son S U, Lee S S, Hyeon T, Chung Y K. Chem Commun, 2001: 2212.
39. Safari J, Banitaba S H, Khalili S D. J Mol Catal A, 2011, 335: 46.
40. Guo F, Zheng H, Yang Z, Qian Y. Mater Lett, 2002, 56: 906.