Novel Synthesis of Some 2-Aminochromene Derivatives using Nano-sized Zirconium Oxide as Catalyst

Organic Preparations and Procedures International

Volumn 48, Issue 1, 2016, Pages 45-54

  Zonouzi, A ^a   Afjei, S J ^a   Rahmani, A ^a   Ng, S W ^b,c  

^a UNIVERSITY OF TEHRAN   (Iran)

^b UNIVERSITY OF MALAYA   (Malaysia)

^c KING ABDULAZIZ UNIVERSITY   (Saudi Arabia)

Author keywords

[No Author keywords available]

Indexed keywords

NANOCATALYSTS;

NANO SIZED; ]+ CATALYST;

ZIRCONIUM COMPOUNDS;

EID: 84956687853     PISSN: 00304948     EISSN: 19455453     Source Type: Journal    
DOI: 10.1080/00304948.2016.1127099     Document Type: Article

References (31)

1. G. P. Ellis. in The Chemistry of Heterocyclic Compounds. Chromenes, Chromanones, and Chromones, Wiley-Interscience, New York, NY, Vol. 100 (2009).
2. M. Curini, G. Cravotto, F. Epifiano, G. Iannone., Curr. Med. Chem., 13, 199 (2006).
3. A. J. Phillips, J. A. Henderson, K. L. Jackson., Comprehensive Heterocyclic Chemistry, Elsevier, 7, 1 (2008).
4. F. Cassidy, J. M. Evans, M. S. Hadel, A. H. Halodij, P. E. Leach, G. Stamp., J. Med. Chem., 35, 1623 (1992).
5. D. W. Roberston, M. F. Steinberg, J. Med. Chem, 33, 1529(1990).
6. B. H. Lee, H. W. Seo, S. E. Yoo., Pharmacology, 70, 74 (2004).
7. X. M. Zhou, Z. B. Zheng, H. Y. Liu, W. Zhong, J. H. Xiao, L. L. Wang, S. Li., Chinese. Chem. Lett., 18, 905 (2007).
8. R. S. Kenny, U. C. Mashelkar, D. M. Rane, D. K. Benzawada., Tetrahedron, 62, 9280 (2006).
9. A. M. Shestopalov, Y. M. Litvinov, L. A. Rodinovskaya, O. R. Malyshev, M. N. Semenova, V. V. Semenov., ACS Comb. Sci., 14 (8), 484 (2012).
10. A. Zonouzi, R. Mirzazadeh, M. Safavi, S. K. Ardestani, S. Emami, A. Foroumadi., Iranian J. Pharm. Res., 12 (4), 679 (2013).
11. T. Timar, K. Zsupan, J. Repasi, I. Borsos, I. Kiss, A. Fodor, P. Maroy., Eur. Pat. Appl. EP 118, 794, Feb, 15 (1983);
12. Chem. Abstr., 102: 45779b (1985).
13. P. Brun, R. Guglielmetti, G. Pepe, S. Anguille., J. Photochem. Photobiol. A. Chem., 156, 77 (2003).
14. H. Hafez, M. Hegab, I. Ahmed-Farag, A. El-Gazzar., Bioorg. Med. Chem. Lett., 18 (16), 4538 (2008).
15. B. Ian, R. Cush, C. J. Groves-Kirby, C. Trundle. US Patent, 4,990,287, Feb, 5 (1991);
16. Chem. Abstr., 108, 158841h (1988).
17. C. M. Starks, R. B. Williams, V. L. Norman, S. M. Rice, M. O'Neil-Johnson, J. A. Lawrence, G. R. Eldridge., Phytochemistry, 98, 216 (2014).
18. J. Mori, M. Iwashima, M. Takeuchi, H. Saito., Chem. Pharm. Bull., 54 (3), 391 (2006).
19. A. Maggini, F. Garzino, P. Brun., J. Photochem. Photobiol A. Chem., 171, 173 (2005).
20. J. Moorthy, P. Venkatakrishnan, S. Sengupta, M. Baidya., Org. Lett., 8, 4891 (2006).
21. S. A. Worlikar, T. Kesharwani, R. C. Larock., J. Org. Chem., 72, 1347 (2007).
22. E. A. A. Wallen, K. Dahlen, M. Grotli, K. Lutheman., Org. Lett., 9, 389 (2007).
23. A. Zonouzi, H. Rahmani, A. Kamali, M. Biniaz., Org. Prep. Proced. Int., 43, 276 (2011).
24. R. K. Gupta, M. V. George., Tetrahedron, 31, 1263 (1975).
25. A. Zonouzi, M. S. Googheri, P. Miralinaghi., Org. Prep. Proced. Int., 40, 471 (2008).
26. A. Zonouzi, Z. Izakian, M. Biniaz, Org. Prep. Proced. Int, 41, 543(2009).
27. A. Zonouzi, F. Hosseinzadeh, N. Karimi, R. Mirzazadeh, S. W. Ng., ACS Comb. Sci., 15 (5), 240 (2013).
28. A. Zonouzi, R. Mirzazadeh, A. Peivandi, S. Dehdari., Heterocycles, 85, 1447 (2012).
29. A. Zonouzi, D. Kazemi, M. Nezamabadi., Org. Prep. Proced. Int., 38, 307 (2006).
30. A. Zonouzi, H. Rahmani, M. Biniaz, Z. Izakian., J. Chem. Res., 222 (2008).
31. Crystallographic data for compound 5a have been deposited with the Cambridge Crystallographic Data Center as supplementary publication No. CCDC 1062691. The data may be obtained free of charge via www.ccdc.com.ac.uk/datarequest/cif.