ZrOCl2·8H2O as an efficient and recyclable catalyst for the clean synthesis of xanthenedione derivatives under solvent-free conditions

Arabian Journal of Chemistry

Volumn 5, Issue 1, 2012, Pages 77-80

  Mosaddegh, Elaheh ^a   Islami, Mohammad Reza ^b   Hassankhani, Asadollah ^c  

^a Khoramshahr Marine Science and Technology University   (Iran)

^b SHAHID BAHONAR UNIVERSITY OF KERMAN   (Iran)

^c International Center for Science High Technology and Environmental Sciences   (Iran)

Author keywords

1,8 Dioxo 1,2,3,4,5,6,7,8 octahydroxanthene; Dimedone; Solvent free condition; XRD; ZrOCl2 8H2O

Indexed keywords

1,8-DIOXO-1,2,3,4,5,6,7,8-OCTAHYDROXANTHENE; AROMATIC ALDEHYDE; CLEAN SYNTHESIS; DIMEDONE; RECYCLABLE CATALYST; SHORT REACTION TIME; SOLVENT FREE CONDITIONS; XANTHENEDIONE DERIVATIVE; XRD; XRD STUDIES;

ALDEHYDES; SOLVENTS; SYNTHESIS (CHEMICAL);

CATALYST ACTIVITY;

EID: 82455220478     PISSN: 18785352     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.arabjc.2010.07.027     Document Type: Article

References (37)

1. Banerjee A., Makherjee A.K. Stain Technol. 1981, 56:83.
2. Casiraghi G., Casnati G., Catellani M., Cornia M. Tetrahedron Lett. 1973, 14:679.
3. Cingolant G.M., Pigini M. J. Med. Chem. 1969, 12:531.
4. Das B., Thirupathi P., Mahender I., Reddy V.S., Rao Y.K. J. Mol. Catal. A 2006, 247:233.
5. Das B., Thirupathi P., Reddy K.R., Ravikanth B., Nagarapu L. Catal. Commun. 2007, 8:535.
6. Eftekhari-Sis B., Abdollahifar A., Hashemi M.M., Zirak M. Eur. J. Org. Chem. 2006, 5152.
7. Fan X., Hu X., Zhang X., Wang J. Can. J. Chem. 2005, 83:16.
8. Firouzabadi H., Iranpoor N., Jafarpour M., Ghaderi A. J. Mol. Catal. 2006, 252:150.
9. Ghosh R., Maiti S., Chakraborty A., Chakraborty S., Mukherjee A.K. Tetrahedron 2006, 62:4059.
10. Hatakeyaa S., Ochi N., Numata H., Takano S. J. Chem. Soc., Chem. Commun. 1988, 1202.
11. Hideu, T., 1981. Jpn. Tokkyo Koho JP 56005480.
12. Hideu T. Chem. Abstr. 1981, 95:80922b.
13. Imani-Shakibaei G., Mirzaei P., Bazgir A. Appl. Catal., A 2007, 325:188.
14. Ion, R.M., Albulescu, C., Sirkecioglu, O., Talinli, N., 2000. Intenet Photochem. Photobiol.
15. Jin S., Zang J.S., Xiao J.C., Wang A.Q., Li T.S. Synlett 2004, 866.
16. Jin T.S., Zhang J.S., Wang A.Q., Li T.S. Synth. Commun. 2005, 35:2339.
17. John A., Yadav P.J.P., Palaniappan S. J. Mol. Catal. A 2006, 248:121.
18. Knight D.W., Little P.B. Synlett 1998, 1141.
19. Knight D.W., Little P.B. J. Chem. Soc., Perkin Trans. 1 2001, 14:1771.
20. Lambert, R.W., Martin, J.A., Merrett, J.H., Parkes, K.E.B., Thomas, G.J., 1997. PCT Int. Appl. WO 9706178.
21. Lambert R.W., Martin J.A., Merrett J.H., Parkes K.E.B., Thomas G.J. Chem. Abstr. 1997, 126:p212377y.
22. Menchen, S.M., Benson, S.C., Lam, J.Y.L., Zhen, W., Sun, D., Rosenblum, B.B., Khan, S.H., Taing, M., 2003. US Patent 6583168.
23. Menchen S.M., Benson S.C., Lam J.Y.L., Zhen W., Sun D., Rosenblum B.B., Khan S.H., Taing M. Chem. Abstr. 2003, 139:54287f.
24. Mosaddegh E., Islami M.R., Hassankhani A. Lett. Org. Chem. 2007, 4:524.
25. O'Callaghan C.N., McMurry T.B.H. J. Chem. Res. 1955, 214.
26. Poupelin J.P., Saint-Rut G., Fussard-Blanpin O., Narcisse G., Uchida-Ernouf G., Lakroix R. Eur. J. Med. Chem. 1978, 13:67.
27. Rakavishnikov A.V., Smith M.P., Birrell G.B., Keana J.F.W., Griffith O.H. Tetrahedron Lett. 1998, 39:6637.
28. Reynolds, G.A., Teccio, S.A., Peterson, O.G., Specht, D.P., 1971. Ger. Offen. DE2109040.
29. Reynolds G.A., Teccio S.A., Peterson O.G., Specht D.P. Chem. Abstr. 1971, 71:p81334c.
30. Robak J., Gryglewski R.J. Pol. J. Parmacol. 1996, 48:555.
31. Rodriguez-Dominguez J.C., Kirsch G. Synthesis 2006, 1895.
32. Seyyedhamzeh M., Mirzaei P., Bazgir A. Dyes Pigm. 2008, 76:836.
33. Shi D.Q., Wang Y.H., Lu Z.S., Dai G.Y. Synth. Commun. 2000, 30:713.
34. Song G., Wang B., Luo H., Yang L. Catal. Commun. 2007, 8:673.
35. Sun H.B., Hua R., Yin Y. Molecules 2006, 11:263.
36. Wang J.Q., Harvey R.G. Tetrahedron 2002, 58:5927.
37. Wang H.K., Morris-Natschke S.L., Lee K.H. Med. Res. Rev. 1997, 17:367.