An efficient synthesis of naphtha[1,2-e]oxazinone and 14-substituted-14H- dibenzo[a,j]xanthene derivatives promoted by zinc oxide nanoparticle under thermal and solvent-free conditions

Tetrahedron Letters

Volumn 53, Issue 22, 2012, Pages 2741-2744

  Dharma Rao, G B ^a   Kaushik, M P ^a   Halve, A K ^b  

^a Discovery Centre   (India)

^b JIWAJI UNIVERSITY   (India)

Author keywords

2 Naphthol; Aldehyde; Heterogeneous catalyst; Naphthoxazinone; Xanthene; Zinc oxide nanoparticles

Indexed keywords

2 NAPHTHOL; ALDEHYDE; HETEROCYCLIC KETONE; NANOPARTICLE; NAPHTHA[1,2 E]OXAZINONE; NAPHTHALENE DERIVATIVE; UNCLASSIFIED DRUG; UREA; XANTHENE DERIVATIVE; ZINC OXIDE NANOPARTICLE;

CHEMICAL REACTION; ISOLATION PROCEDURE; NANOCHEMISTRY; REVIEW; SYNTHESIS;

HUMAN ECHOVIRUS 1;

EID: 84860215491     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2012.03.085     Document Type: Article

References (32)

1. M. Patel, R.J. McHugh Jr., B.C. Cordova, R.M. Klabe, S. Erickson-Viitanen, G.L. Trainor, and S.S. Koo Bioorg. Med. Chem. Lett. 9 1999 3221
2. L. Waxman, and P.L. Darke Antiviral Chem. Chemother. 11 2000 1
3. N. Latif, N. Mishriky, and F.M. Assad Aust. J. Chem. 35 1982 1037
4. Y. Wang, X. Li, and K. Ding Tetrahedron: Asymmetry 13 2002 1291
5. F.W. Holly, and A.C. Cope J. Am. Chem. Soc. 66 1944 1875
6. I. Szatmari, A. Hetenyi, L. Lazar, and F. Fulop J. Heterocycl. Chem. 41 2004 367
7. C. Cimarelh, G. Palmieri, and E. Volpini Can. J. Chem. 82 2004 1314
8. M. Dabiri, A.S. Delbari, and A. Bazgir Synlett 2007 821
9. G. Sabitha, K. Arundhathi, K. Sudhakar, and B.S. Sastry J. Heterocycl. Chem. 47 2010 272
10. K. Srinivas, V.V.N. Srinivasu, B. Rajashaker, and N. Linghaiah J. Heterocycl. Chem. 47 2010 313
11. M.H. Mosslemin, M.R. Nateghi, and R. Mohebat Monatsh. Chem. 139 2008 1247
12. Y.N. Xia, P.D. Yang, Y.G. Sun, Y.Y. Wu, B. Mayers, B. Gates, Y.D. Yin, F. Kin, and H.Q. Yan Adv. Mater. 15 2003 353
13. M. Hosseini-Sarvari, and S. Etemad Tetrahedron 64 2008 5519
14. M. Hosseini-Sarvari, H. Sharghi, and S. Etemad Helv. Chim. Acta 91 2008 715
15. Z. Mirjafary, H. Saeidian, A. Sadeghi, and F.M. Moghaddam Catal. Commun. 9 2008 299
16. M.Z. Kassaee, H. Masrouri, and F. Movahedi Monatsh. Chem. 141 2010 317 322
17. G.K. Prasad, P.V.R.K. Ramacharyulu, B. Singh, K. Batra, A.R. Srivastava, K. Ganesan, and R. Vijayaraghavan J. Mol. Catal. A: Chem. 349 2011 55
18. H.N. Karade, M. Sathe, and M.P. Kaushik ARKIVOC xiii 2007 252 258
19. G.B. Dharma Rao, B.N. Acharya, S.K. Verma, and M.P. Kaushik Tetrahedron Lett. 52 2011 809 812
20. A. Banerjee, and A.K. Mukherjee Stain Technol. 56 1981 83
21. O. Sirkeeioglu, N. Talinli, and A. Akar J. Chem. Res. (S) 1995 502
22. M. Ahmad, T.A. King, D.-K. Ko, B.H. Cha, and J. Lee J. Phys. D: Appl. Phys. 35 2002 1473
23. C.G. Knight, and T. Stephens Biochem. J. 258 1989 683
24. R.W. Lambert, J.A. Martin, J.H. Merrett, K.E.B. Parkes, and G.J. Thomas Chem. Abstr. 126 1997 p212377y
25. Hideo, T. Jpn. Tokkyo Koho JP 56005480, 1981; Chem. Abstr. 1981, 95, 80922b.
26. J.P. Poupelin, G. Saint-Rut, O. Foussard-Blanpin, G. Narcisse, G. Uchida-Ernouf, and R. Lacroix Eur. J. Med. Chem. 13 1978 67
27. G. Saint-Ruf, A. De, and H.T. Hieu Bull. Chim. Ther. 7 1972 83 86
28. R.M. Ion, D. Frackowiak, A. Planner, and K. Wiktorowicz Acta Biochim. Pol. 45 1998 833 845
29. M.A. Bigdeli, M.M. Heravi, and G.H. Mahdavinia Catal. Commun. 8 2007 1595
30. B. Maleki, M. Gholizadeh, and Z. Sepehr Bull. Korean Chem. Soc. 32 2011 1697 1702
31. B.B.F. Mirjalili, A. Bamoniri, and A. Akbari Tetrahedron Lett. 49 2008 6454 6456
32. B. Rajitha, B.S. Kumar, Y.T. Reddy, P.N. Reddy, and N. Sreenivasulu Tetrahedron Lett. 46 2005 8691