Molecular iodine catalyzed synthesis of aryl-14H-dibenzo[a, j]xanthenes under solvent-free condition

Bioorganic and Medicinal Chemistry Letters

Volumn 17, Issue 3, 2007, Pages 621-623

  Pasha, Mohamed A ^a   Jayashankara, Vaderapura P ^a  

^a BANGALORE UNIVERSITY   (India)

Author keywords

Naphthol; Araldehydes; Aryl 14H dibenzo a, j xanthenes; Solvent free condition

Indexed keywords

2 NAPHTHOL; ALDEHYDE; IODINE; XANTHENE DERIVATIVE;

ARTICLE; CATALYSIS; CHEMICAL REACTION; DRUG SYNTHESIS;

CATALYSIS; IODINE; MAGNETIC RESONANCE SPECTROSCOPY; NAPHTHOLS; SOLVENTS; SPECTROPHOTOMETRY, INFRARED; XANTHENES;

EID: 33846240529     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2006.11.009     Document Type: Article

References (24)

1. Hideo, T. Chem. Abstr. 1981, 95, 80922b, Jpn. Tokkyo Koho JP 56005480, 1981.
2. Lambert, R. W.; Martin, J. A.; Merrett, J. H.; Parker, K. E. B.; Thomas, G. J. PCT Int. Appl. WO9706178, 1997.
3. Poupelin J.P., Ruf G.S., Blanpin O.F., Narcisse G., Ernouf G.U., and Lacroix R. Eur. J. Med. Chem. 13 (1978) 67
4. Ion R.M., Albulescu C., Sirkecioglu O., and Talinli N. Intenet. Photochem. Photobiol. (2000)
5. Menchen, S. M.; Benson, S. C.; Lam, J. Y. L.; Zhen, W.; Sun, D.; Rosenblum, B. B.; Khan, S. H.; Taing, M. U.S. Patent 6,583, 168, 2003.
6. Banerjee A., and Mukherjee A.K. Stain Technol. 56 (1981) 83
7. Bekaert A., Andrieux J., and Plat M. Tetrahedron Lett. 33 (1992) 2805
8. Sarma R.J., and Baruah J.B. Dyes Pigments 64 (2005) 91
9. Buehler C.A., Cooper D.E., and Scrudder E.O. J. Org. Chem. 8 (1943) 316
10. Licudine P.J.A., Kawate M.K., and Li Q.X. J. Agric. Food Chem. 45 (1997) 766
11. Wang J.Q., and Harvey R.G. Tetrahedron 58 (2002) 5927
12. Knignt D.W., and Little P.B. J. Chem. Soc., Pertin Trans. 1 14 (2001) 1771
13. Knignt D.W., and Little P.B. Synlett (1998) 1141
14. Casiraghi G., Casnati G., Catellani M., and Cornia M. Tetrahedron Lett. 14 (1973) 679
15. Buu-Hoi N.P., and Xuong N.D. J. Org. Chem. 16 (1951) 1633
16. Zad A.K., Kazemi Z., and Rudbari H.A. J. Korean Chem. Soc. 46 (2002) 541
17. Rajitha B., Sunil Kumar B., Reddy Y.T., Reddy P.N., and Sreenivasulu N. Tetrahedron Lett. 46 (2005) 8691 Sulfamic acid catalysed synthesis of aryl-14H-dibenzo[a, j]xanthenes under conventional heating and under microwave irradiation is reported, the reactions take 6-12 h for completion under conventional heating at 125 °C
18. 2 on heating at 190 °C requires more than 4 h for completion, and gives a mixture of products.
19. Ahmad K.Z., Akbari S.A., Azam S., and Hojat V. J. Chem. Res. (S) (2005) 277 14H-Dibenzo[a, j]xanthene derivatives are prepared under microwave irradiation in the presence of p-toluenesulfonic acid and the yields are low in a few cases.
20. Khosropour A.R., Khodaei M.M., and Moghannian H. Synlett (2005) 955
21. Zhang Z., and Liu Q. Prog. Chem. 18 (2006) 270
22. Pasha M.A., and Jayashankara V.P. Synth. Commun. 36 (2006) 1787
23. Myint Y.Y., and Pasha M.A. Synth. Commun. 34 (2004) 4477
24. +)].