Oxybromination of ethynylbenzene catalysed by molybdenum complexes in organic solvent and in ionic liquids

Advanced Synthesis and Catalysis

Volumn 347, Issue 10, 2005, Pages 1341-1344

  Conte, Valeria ^a   Floris, Barbara ^a   Galloni, Pierluca ^a   Silvagni, Adriano ^a  

^a UNIVERSITY OF ROME TOR VERGATA   (Italy)

Author keywords

Alkynes; Green chemistry; Ionic liquids; Molybdenum(VI); Oxybromination

Indexed keywords

EID: 24644492410     PISSN: 16154150     EISSN: None     Source Type: Journal    
DOI: 10.1002/adsc.200505114     Document Type: Article

References (25)

1. a) F. Diederich, P. J. Stang, R. R. Tykwinski (Eds.), Acetylene Chemistry, VCH-Wiley, Weinheim, 2005;
2. b) P. J. Stang, F. Diederich, (Eds.), Modern Acetylene Chemistry, VCH-Wiley, Weinheim, 1995.
3. V. Conte, F. Di Furia, S. Moro, Tetrahedron Lett. 1994, 35, 7429.
4. M. Andersson, V. Conte, F. Di Furia, S. Moro Tetrahedron Lett. 1995, 36, 2675.
5. V. Conte, F. Di Furia, S. Moro, S. Rabbolini J. Mol. Cat. A: Chem. 1996, 113, 175.
6. V. Conte, B. Floris, P. Galloni, A. Silvagni, Pure Appl. Chem. in press.
7. K. Yates, G. H. Schmid, T. W. Regulski, D. G. Garratt, H.-W. Leung, R. McDonald, J. Am. Chem. Soc. 1973, 95, 160.
8. V. Conte, F. Di Furia, S. Moro, Tetrahedron Lett. 1996, 37, 8609.
9. V. Conte, F. Di Furia, S. Moro, J. Mol. Cat. A: Chem. 1997, 117, 139.
10. P. Wasserscheid, T. Welton, Ionic Liquids in Synthesis, Wiley-VCH, Weinheim, 2003.
11. See, for example: a) H. Luthardt, C. Fieseler, M. Wind, W. Kochmann, W. Kramer, K. Naumann, E. Schiewald, U. Thust, German Patent DD82-242506 19820813; 1984, Chem. Abstr. 1984, 102, 57820;
12. b) D. R. Arneklev, F. M. Pallos, E. Gaughan, US Patent US 74-527662 19741125, 1976; Chem. Abstr. 1976, 85, 155078;
13. c) D. R. Baker, German Patent DE 71-2156625 19711115, 1972; Chem. Abstr. 1972, 77, 122996.
14. Y. Aoki, K. Oshima, K. Utimoto, Synlett 1995, 1071.
15. S. Paul, V. Gupta, R. Gupta, A. Loupy, Tetrahedron Lett. 2003, 44, 439 and references cited therein.
16. J. A. Nobrega, S. M. C. Gonçalves, C. Peppe, Synth. Commun. 2002, 32, 3711.
17. O. Bortolini, M. Carraro, V. Conte, S. Moro, Eur. J. Inorg. Chem. 2003, 42.
18. L. Crowhurst, P. R. Mawdsley, J. M. Perez-Arlandis, P. A. Salter, T. Welton, Phys. Chem. Chem. Phys. 2003, 5, 2790.
19. H. Masuda, K. Takase, M. Nishio, A. Hasegawa, Y. Nishiyama, Y. Ishii, J. Org. Chem. 1994, 59, 5550.
20. V. Farmer, T. Welton, Green Chem. 2002, 4, 97.
21. G. S. Owens, M. M. Abu Omar, J. Mol. Cat. A: Chem. 2002, 187, 215.
22. P. A. Z. Suarez, J. E. L. Dullius, S. Einloft, R. F. de Souza, J. Dupont, Polyhedron 1996, 15, 1217.
23. P. A. Z. Suarez, S. Einloft, J. E. L. Dullius, R. F. De Souza, J. Dupont, J. Chim. Phys. 1998, 1626.
24. L. Cammarata, S. G. Kazarian, P. A. Salter, T. Welton, Phys. Chem. Chem. Phys. 2001, 3, 5192.
25. C. Chiappe, V. Conte, D. Pieraccini, Eur. J. Org. Chem. 2002, 2831.