Simple and efficient one-pot synthesis of imidazo[1,2-a]pyridines catalyzed by magnetic nano-Fe 3O 4-KHSO 4·SiO 2

Synlett

Volumn 23, Issue 18, 2012, Pages 2635-2638

  Guntreddi, Tirumaleswararao ^a   Allam, Bharat Kumar ^a   Singh, Krishna Nand ^a  

^a BANARAS HINDU UNIVERSITY   (India)

Author keywords

heterocycles; heterogeneous catalysis; iron; multicomponent reactions; transition metals

Indexed keywords

3 BENZYL 2 (3 CHLOROPHENYL)IMIDAZO[1,2 A]PYRIDINE; 3 BENZYL 2 (4 TOLYL)IMIDAZO[1,2 A]PYRIDINE; IMIDAZO[1,2 A]PYRIDINE DERIVATIVE; MAGNETIC NANOPARTICLE; ULTRASMALL SUPERPARAMAGNETIC IRON OXIDE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL BOND; CHEMICAL REACTION KINETICS; DRUG STRUCTURE; DRUG SYNTHESIS; ONE POT SYNTHESIS;

EID: 84866793469     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0032-1317323     Document Type: Article

References (26)

1. Zhu J., Bienaymé H. Multicomponent Reactions. Wiley-VCH Weinheim: 2005
2. Dömling A., Wang W., Wang K. Chem. Rev.: 2012; 112 3083
3. Horton D. A., Bourne G. T., Smythe M. L. Chem. Rev.: 2003; 103 893
4. Constantino L., Barlocco D. Curr. Med. Chem.: 2006; 13 65
5. Oishi H., Takano K.-i, Tomita K., Takebe M., Yokoo H., Yamazaki M., Hattori Y. Am. J. Physiol. Lung Cell Mol. Physiol.: 2012; 303 L130
6. Yamane I., Hagino H., Okano T., Enokida M., Yamasaki D., Teshima R. Arthritis Rheum.: 2003; 48 1732
7. Kim O., Jeong Y., Lee H., Hong S.-S, Hong S. J. Med. Chem.: 2011; 54 2455
8. Trabanco A. A., Tresadern G., Macdonald G. J., Vega J. A., de Lucas A. I., Matesanz E., García A., Linares M. L., de Diego S. A. A, Alonso J. M., Oehlrich D., Ahnaou A., Drinkenburg W., Mackie C., Andres J. I., Lavreysen H., Cid J. M. J. Med. Chem.: 2012; 55 2688
9. Kamal A., Surendranadha Reddy J., Janaki Ramaiah M., Dastagiri D., Vijaya Bharathi E., Victor Prem Sagar M., Pushpavalli S. N. C. V. L, Ray P., Pal-Bhadra M. Med. Chem. Commun.: 2010; 1 355
10. Langer S. Z., Arbilla S., Benavides J., Scatton B. Adv. Biochem. Psychopharmacol.: 1990; 46 61
11. Lhassani M., Chavignon O., Chezal J.-M, Teulade J.-C, Chapat J.-P, Snoeck R., Andrei G., Balzarini J., De Clercq E., Gueiffier A. Eur. J. Med. Chem.: 1999; 34 271
12. Chernyak N., Gevorgyan V. Angew. Chem. Int. Ed.: 2010; 49 2743
13. Reddy B. V. S, Reddy P. S., Reddy Y. J., Yadav J. S. Tetrahedron Lett.: 2011; 52 5789
14. Liu P., Fang L.-s, Lei X., Lin G.-q. Tetrahedron Lett.: 2010; 51 4605
15. Mishra S., Ghosh R. Synthesis: 2011; 3463
16. Polshettiwar V., Luque R., Fihri A., Zhu H., Bouhrara M., Basset J. M. Chem. Rev.: 2011; 111 3036
17. Shylesh S., Schunemann V., Thiel W. R. Angew. Chem. Int. Ed.: 2010; 49 3428
18. Firouzabadi H., Iranpoor N., Gholinejad M., Hoseini J. Adv. Synth. Catal.: 2011; 353 125
19. Zhang Z.-H, Lu H.-Y, Yang S.-H, Gao J.-W. J. Comb. Chem.: 2010; 12 643
20. Martínez R., Ramón D. J., Yus M. Adv. Synth. Catal.: 2008; 350 1235
21. Allam B. K., Singh K. N. Tetrahedron Lett.: 2011; 52 5851
22. Allam B. K., Singh K. N. Synthesis: 2011; 1125
23. Singh N., Singh S. K., Khanna R. S., Singh K. N. Tetrahedron Lett.: 2011; 52 2419
24. Kumari K., Raghuvanshi D. S., Jouikov V., Singh K. N. Tetrahedron Lett.: 2012; 53 1130
25. Raghuvanshi D. S., Singh K. N. Tetrahedron Lett.: 2011; 52 5702
26. Raghuvanshi D. S., Singh K. N. Synlett: 2011; 373