An efficient synthesis of ferrocenyl substituted 1,5-diketone and cyclic α,β-unsaturated ketones under ultrasound irradiation

Journal of Organometallic Chemistry

Volumn 689, Issue 10, 2004, Pages 1843-1848

  Ji, Shun Jun ^a   Shen, Zhi Liang ^a   Gu, Da Gong ^a   Wang, Shun Yi ^a  

^a SOOCHOW UNIVERSITY   (China)

Author keywords

1,5 Diketone; Chalcone; Crystal structure; Ferrocene; Michael reaction; Ultrasound

Indexed keywords

BENZENE DERIVATIVE; CHALCONE DERIVATIVE; FERROCENE DERIVATIVE; KETONE DERIVATIVE; ORGANOMETALLIC COMPOUND; SODIUM HYDROXIDE;

ARTICLE; CATALYSIS; CHEMICAL ANALYSIS; CHEMICAL MODIFICATION; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; CONTROLLED STUDY; CRYSTAL STRUCTURE; METHODOLOGY; MICHAEL ADDITION; QUANTUM YIELD; STRUCTURE ANALYSIS; SYNTHESIS; ULTRASOUND; X RAY CRYSTALLOGRAPHY;

EID: 1942472013     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jorganchem.2004.03.006     Document Type: Article

References (30)

1. Ariyan Z.S. Suschitzky H. J. Chem. Soc. 1961 2242
2. Hirsch S.S. Bailey W.J. J. Org. Chem. 43 1978 4091
3. Krohnke F. Synthesis 1976 1
4. Constable E.C. Cargill Thompson A.M.W. J. Chem. Soc., Dalton Trans. 1992 2947
5. Potts K.T. Bull. Soc. Chem. Belg. 99 1990 741
6. Butler I.R. Mcdonald S.J. Polyhedron 14 1995 529
7. Gill N.S. James K.B. Lions F. Potts K.T. J. Am. Chem. Soc. 74 1952 4923
8. James G. Robert H. Jadwiga T.G. J. Chem. Soc., Perkin Trans. 1 1982 229
9. Junko S. Mami N. Hajime N. Koko M.J. Chem. Soc., Perkin Trans. 2 1988 1607
10. Hutchins W.A. Motwani D.C. Mudbhatkal K.D. Wheeler T.S. J. Chem. Soc. 1938 1882
11. Robison M.M. Pierson W.G. Orfman L.D. Lambert B.F. J. Org. Chem. 31 1966 3213
12. Chapurlat R. Dreux J. Bull. Soc. Chim. Fr. 1962 349
13. Vilardo J.S. Lockwood M.A. Hanson L.G. Clark J.R. Parkin B.C. J. Chem. Soc., Dalton Trans. 18 1997 3353
14. Bock H. John A. Kleine M. Naether C. Bats J.W.Z. Naturforsch. B 49 1994 529
15. Essawy A.I. Elkady M. Mohamed A.Y. Ind. J. Chem. Sect. B 19 1980 567-570
16. El-Hashash M.A. Essawy A. Ind. J. Chem. Sect. B 17 1979 454-457
17. Lickiss P.D. Lucas R. J. Organomet. Chem. 521 1995 229
18. Li J.-T. Yang W.-Z. Wang S.-X. Li S.-H. Li T.-S. Ultrason. Sonochem. 9 2002 237
19. Wang S.-X. Li J.-T. Yang W.-Z. Li T.-S. Ultrason. Sonochem. 9 2002 159
20. Raimundo B.C. Fry A.J. J. Organomet. Chem. 584 1999 230
21. Ando T. Cork D.G. Kimura T. Chem. Lett. 173 1986 665
22. Qin Z. Chen F. Xie Y. Progr. Chem. 10 1998 65
23. Li J.-T. Li L.-J. Li T.-S. Li H.-Z. Li J.-K. Ultrason. Sonochem. 3 1996 141
24. Fuentes A. Sinisterra J.V. Tetrahedron Lett. 27 1986 2967
25. Jayasree J. Rao J.M. Synth. Commun. 26 1996 3717
26. Harrity J.P.A. Kerr W.J. Middlemiss D. Scott J.S. J. Organomet. Chem. 532 1997 219
27. Winum J.Y. Kamal M. Leydet A. Tetrahedron Lett. 37 1996 178
28. Li J.-T. Li T.-S. Li L.-J. Cheng X. Ultrason. Sonochem. 6 1999 199
29. Liu W.-Y. Xu Q.-H. Liang Y.-M. Chen B.-H. Liu W.-M. Ma Y.-X. J. Organomet. Chem. 637-639 2001 719
30. Ji S.-J. Shen Z.-L. Wang S.-Y. Chin. Chem. Lett. 14 2003 663