KSF supported 10-molybdo-2-vanadophosphoric acid as an efficient and reusable catalyst for one-pot synthesis of 2,4,5-trisubstituted imidazole derivatives under solvent-free condition

Cuihua Xuebao/Chinese Journal of Catalysis

Volumn 36, Issue 7, 2015, Pages 1054-1059

  Chavan, Laxmikant D ^a   Shankarwar, Sunil G ^a  

^a DR BABASAHEB AMBEDKAR MARATHWADA UNIVERSITY   (India)

Author keywords

10 Molybdo 2 vanadophosphoric acid; 2,4,5 Trisubstituted imidazole; Heterogeneous catalyst; Heteropoly acid; KSF clay

Indexed keywords

CATALYST ACTIVITY; CATALYSTS; THERMOANALYSIS;

2,4,5-TRISUBSTITUTED IMIDAZOLE; HETEROGENEOUS CATALYST; HETEROPOLY ACIDS; IMIDAZOLE DERIVATIVES; RECYCLABLE CATALYST; REUSABLE CATALYSTS; SHORT REACTION TIME; SOLVENT FREE CONDITIONS;

CATALYST SUPPORTS;

EID: 84934997097     PISSN: 02539837     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1872-2067(15)60830-0     Document Type: Article

References (30)

1. Sheldon R A. Green Chem, 2007, 9: 1273
2. Tang S Y, Bourne R A, Smith R L, Poliakoff M. Green Chem, 2008, 10: 268
3. Kozhevnikov I V. Russ Chem Rev, 1993, 62: 473
4. Dias J A, Osegovic J P, Drago R S. J Catal, 1999, 183: 83
5. Kozhevnikov I V. Catalysis for Fine Chemical Synthesis, Vol. 2. Chichester: Wiley, 2002
6. Kozhevnikov I V. Appl Catal A, 2003, 256: 3
7. Chimienti M E, Pizzio L R, Caceres C V, Blanco M N. Appl Catal A, 2001, 208: 7
8. Shelke K F, Sapkal S B, Sonar S S, Madje B R, Shingte B B, Shingare M S. Bull Korean Chem Soc, 2009, 30: 1057
9. Wang L, Woods K W, Li Q, Barr K J, McCroskey R W, Hannick S M, Gherke L, Credo R B, Hui Y H, Marsh K, Warner R, Lee J Y, Zielinsky-Mozng N, Frost D, Rosenberg S H, Sham H L. J Med Chem, 2002, 45: 1697
10. Mohammadi A, Keshvari H, Sandaroos R, Rouhi H, Sepehr Z. J Chem Sci, 2012, 124: 717
11. Joshi R S, Mandhane P G, Shaikh M U, Kale R P, Gill C H. Chin Chem Lett, 2010, 21: 429
12. Ucucu U, Karaburun N G, Isikdag I. Farmaco, 2001, 56: 285
13. Ashrafi M, Davoodnia A, Tavakoli-Hoseini N. Bull Korean Chem Soc, 2013, 34: 1508
14. De Laszlo S E, Hacker C, Li B, Kim D, MacCoss M, Mantlo N, Pivnichny J V, Colwell L, Koch G E, Cascieri M A, Hagmann W K. Bioorg Med Chem Lett, 1999, 9: 641
15. Gadekar L S, Mane S R, Katkar S S, Arbad B R, Lande M K. Cent Eur J Chem, 2009, 7: 550
16. Balalaie S, Arabanian A, Hashtroudi M S. Monatsh Fur Chem, 2000, 131: 945
17. Radziszewski B. Chem Ber, 1882, 15: 1493
18. Japp F, Robinson H. Chem Ber, 1882, 15: 1268
19. Sharma G V M, Jyothi Y, Lakshmi P S. Synth Commun, 2006, 36: 2991
20. Ahmad S, Abbas R, Elham F, Zahra B. Catal Commun, 2007, 8: 1149
21. Shojaei A F, Rezvani M A, Baei M S. World Appl Sci J, 2010, 11: 727
22. Karimi A R, Alimohammadi Z, Amini M M. Mol Divers, 2010, 14: 635
23. Wang L M, Wang Y H, Tian H, Yao Y F, Shao J H, Liu B. J Fluorine Chem, 2006, 127: 1570
24. Mohammadi A A, Mivechi M, Kefayati H. Monatsh Chem, 2008, 139: 935
25. Samai S, Nandi G C, Singh P, Singh M S. Tetrahedron, 2009, 65: 10155
26. Chuanming Y, Min L, Weike S, Yuan Y X. Synth Commun, 2007, 37: 3304
27. Sangshetti J N, Kokare N D, Kotharkar S A, Shinde D B. Monatsh Chem, 2008, 139: 125
28. Samai S, Nandi G C, Singh P, Singh M S. Tetrahedron Lett, 2009, 65: 10155
29. Sangshetti J N, Kokare N D, Kotharkara S A, Shinde D B. J Chem Sci, 2008, 120: 463
30. Shaabani A, Rahmati A, Farhangi E, Badri Z. Catal Commun, 2007, 8: 1149