Dowex-50W promoted synthesis of 14-aryl-14H-dibenzo[a,j]xanthene and 1,8-dioxo-octahydroxanthene derivatives under solvent-free conditions

Applied Catalysis A: General

Volumn 325, Issue 1, 2007, Pages 188-192

  Shakibaei, Gazaleh Imani ^a   Mirzaei, Peiman ^a   Bazgir, Ayoob ^a  

^a SHAHID BEHESHTI UNIVERSITY   (Iran)

Author keywords

Dowex 50W; Naphthol; Reusable catalyst; Solvent free; Xanthene

Indexed keywords

CATALYSTS; ION EXCHANGE; RESINS; SOLVENTS; SYNTHESIS (CHEMICAL);

DOWEX 50W; NAPHTHOL; REUSABLE CATALYST; XANTHENE;

AROMATIC COMPOUNDS;

EID: 34248223139     PISSN: 0926860X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apcata.2007.03.008     Document Type: Article

References (26)

1. Olah G.A. In: Fraissard J., and Petrakis L. (Eds). Acidity and Basicity of Solids (1994), Kluwer, Dortrecht, Netherlands 305-334
2. Izumi Y., Urabe K., and Onaka M. Zeolite, Clay and Heteropoly Acids in Organic Reactions (1992), VCH, New York
3. Singh K., Arora D., and Singh S. Tetrahedron Lett. 47 (2006) 4205-4207
4. Kidwai M., Mohan R., and Rastogi S. Synth. Commun. 33 (2003) 3747-3759
5. Bacci J.P., Kearney A.M., and Van Vranken D.L. J. Org. Chem. 70 (2005) 9051-9053
6. Schneider H.J., Guttes D., and Schneider U. J. Am. Chem. Soc. 110 (1988) 6449-6459
7. Gutsche C.D. Calixarenes' Cambridge (1989), The Royal Society of Chemistry
8. Handique J.G., and Baruah J.B. React. Funct. Polym. 52 (2002) 163-188
9. Banerjee A., and Mukherjee A.K. Stain Technol. 56 (1981) 83-85
10. Sirkecioglu O., Tulinli N., and Akar A. J. Chem. Res. (S) (1995) 502
11. knight C.G., and Stephenes T. Biochem. J. 258 (1989) 683-689
12. T. Hideu, Jpn. Tokkyo Koho JP 56005480, 1981 (Chem. Abstr. 95 (1981) 80922b).
13. R.W. Lamberk, J.A. Martin, J.H. Merrett, K.E.B. Parkes, G.J. Thomas, PCT Int. Appl. WO 9706178, 1997 (Chem. Abstr. 126 (1997) P212377y).
14. Poupelin J.P., Saint-Rut G., Fussard-Blanpin O., Narcisse G., Uchida-Ernouf G., and Lakroix R. Eur. J. Med. Chem. 13 (1978) 67-71
15. Kumar P.S., Kumar B.S., Rajitha B., Reddy P.N., Sreenivasulu N., and Reddy Y.T. Arkivoc xii (2006) 46-50
16. Khosropour A.R., Khodaei M.M., and Moghannian H. Synlett (2005) 955-958
17. Das B., Ravikanth B., Ramu R., Laxminarayana K., and Vittal Rao B. J. Mol. Catal. A: Chem. 255 (2006) 74-77
18. Rajitha B., Kumar B.S., Reddy Y.T., Reddy P.N., and Sreenivasulu N. Tetrahedron Lett. 46 (2005) 8691-8693
19. Sarma R.J., and Baruah J.B. Dyes Pigm. 64 (2005) 91-92
20. Knight D.W., and Little P.B. J. Chem. Soc. Perkin Trans. I 14 (2001) 1771-1777
21. Jha A. J. Beal Tetrahedron Lett. 45 (2004) 8999-9001
22. Sen R.N., and Surkar N.N. J. Am. Chem. Soc. 47 (1925) 1079-1091
23. Papini P., and Cimmarusti R. Gazz. Chim. Ital. 77 (1947) 142-145
24. Ota K., and Kito T. Bull. Chem. Soc. Jpn. 49 (1978) 1167-1168
25. Mohammadpour Amini M., Shaabani A., and Bazgir A. Catal. Commun. 7 (2006) 843-847
26. Bazgir A. J. Chem. Res. (S) (2006) 1-2