Solvent free synthesis of 1,3-diaryl-2-propenones catalyzed by commercial acid-clays under ultrasound irradiation

Ultrasonics Sonochemistry

Volumn 17, Issue 1, 2010, Pages 246-249

  Chtourou, Manef ^a   Abdelhédi, Rami ^a   Frikha, Mohamed Hédi ^a   Trabelsi, Mahmoud ^a  

^a University of Sfax   (Tunisia)

Author keywords

Acid montmorillonites; Solvent free; trans Chalcones; Ultrasound

Indexed keywords

CLAY MINERALS; IRRADIATION; KETONES; ULTRASONICS;

ARYL ALDEHYDES; CHALCONES; METHYL KETONES; NOVEL SOLVENTS; SHORT REACTION TIME; SOLVENT FREE; SOLVENT FREE SYNTHESIS; ULTRASOUND IRRADIATION;

SOLVENTS;

ACID; ALDEHYDE DERIVATIVE; CHALCONE DERIVATIVE; KETONE DERIVATIVE; MONTMORILLONITE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; PROPYLENE; SOLVENT;

ARTICLE; CATALYSIS; CATALYST; CLAY; PRIORITY JOURNAL; QUANTUM YIELD; REACTION ANALYSIS; REACTION TIME; SYNTHESIS; ULTRASOUND;

ACIDS; ALUMINUM SILICATES; CATALYSIS; CHALCONES; RADIATION DOSAGE; SOLVENTS; SONICATION;

EID: 69949187975     PISSN: 13504177     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ultsonch.2009.06.008     Document Type: Article

References (30)

1. Ballini R., Bosica G., Maggi R., Ricciutelli M., Righi P., Sartori G., and Sartorio R. Green Chem. 3 (2001) 178
2. Li J.T., Yang W.Z., Wang S.X., Li S.H., and Li T.S. Ultrason. Sonochem. 9 (2002) 237
3. Liu M., Wilairat P., and Go M.-L. J. Med. Chem. 44 (2001) 4443
4. Dominguez J.N., Charris J.E., Lobo G., de Dominguez N.G., Moreno M.M., Riggione F., Sanchez E., Olson J., and Rosenthal P.J. Eur. J. Med. Chem. 36 (2001) 555
5. Xia Y., Yang Z.Y., Xia P., Bastow K.F., Nakanishi Y., and Lee K.H. Bioorg. Med. Chem. Lett. 10 (2000) 699
6. Zhai L., Chen M., Blom J., Theander T.G., Christensen S.B., and Kharazmi A. J. Antimicrob. Chemother. 43 (1999) 793
7. Hsieh H.K., Tsao L.T., and Wang J.P. J. Pharm. Pharmacol. 52 (2000) 163
8. Ducki S., Forrest R., Hadfield J.A., Kendall A., Lawrence N.J., McGown A.T., and Rennison D. Bioorg. Med. Chem. Lett. 8 (1998) 1051
9. Lin L.M., Zhou Y., Flavin M.T., Zhou L.M., Nie W., and Chen F.C. Bioorg. Med. Chem. 10 (2002) 2795
10. Furman C., Lebeau J., Fruchart J.C., Bernier J.L., Duriez P., Cotelle N., and Teissier E. J. Biochem. Mol. Toxicol. 15 (2001) 270
11. Park E.J., Park R., Lee J.S., and Kim J. Planta Med. 64 (1998) 464
12. Cave G.W., and Raston C.L. Chem. Commun. (2000) 2199
13. Le Gal E., Texier-Boullet F., and Hamelien J. Synth. Commun. 29 (1999) 3651
14. Kloetstra K.R., and van Bekkum H. J. Chem. Soc., Chem. Commun. (1995) 1005
15. Natekar R.S., and Samant S.D. Indian J. Chem. Sect. B 30 (1994) 313
16. Wachter-Jurcsak N., Radu C., and Redin K. Tetrahedron Lett. 39 (1998) 3903
17. Yadav M.K., Chudasama C.D., and Jasra R.V. J. Mol. Catal., A Chem. 216 (2004) 51
18. Hart M.P., and Brown D.R. J. Mol. Catal., A Chem. 212 (2004) 315
19. Jasra R.V. Bull. Catal. Soc. India 2 (2003) 157
20. Moussaoui Y., and Ben Salem R. C.R. Chim. 10 (2007) 1162-1169
21. Vodnár J., Farkas J., and Békássy S. Appl. Catal., A Gen. 208 (2001) 329-334
22. Calvino V., Picallo M., Lopez-Peinado A.J., Martin-Aranda R.M., and Duran-Valle C.J. Appl. Surf. Sci. 252 (2006) 6071-6074
23. Duran-Valle C.J., Fonseca I.M., Calvino-Casilda V., Picallo M., Lopez-Peinado A.J., and Martin-Aranda R.M. Catal. Today 107-108 (2005) 500-506
24. Entezari M.H., and Kauus P. Ultrason. Sonochem. 3 (1996) 19
25. Raso J., Manas P., Pagan R., and Sala F.J. Ultrason. Sonochem. 5 (1999) 157
26. Irie K., and Watanabe K. Bull. Chem. Soc. Jpn. 53 (1980) 1366
27. Xu Q., Yang Z., Yin D., and Zhang F. Catal. Commun. 9 (2008) 1579-1582
28. Bhagat S., Sharma R., Sawant D.M., Sharma L., and Chakraborti A.K. J. Mol. Catal., A Chem. 244 (2006) 20-24
29. Silverstein R.M., Bassler G.C., and Morrill T.C. Spectroscopic Identification of Organic Compounds. fifth ed. (1991), John Wiley, Singapore
30. K.R. Makham, H. Geiger, in: J.B. Harborne (Ed.), The Flavonoids, Advances in Research Since 1986, Chapman and Hall/CRC, London, p 447.