Heterogeneous hydrogenation of substituted phenols over Al2O3 supported ruthenium

Journal of Molecular Catalysis A: Chemical

Volumn 273, Issue 1-2, 2007, Pages 92-98

  Solladie Cavallo A ^a   Baram, A ^a   Choucair, E ^a   Norouzi Arasi, H ^a   Schmitt, M ^a   Garin, F ^b  

^a CNRS   (France)

^b UNIVERSITÉ DE STRASBOURG   (France)

Author keywords

Hydrogenation of disubstituted phenols; Hydrogenation of monosubstituted phenols; Ruthenium hydrogenation

Indexed keywords

ALUMINA; CATALYST ACTIVITY; HYDROGENATION; ISOMERS; RUTHENIUM; SUBSTITUTION REACTIONS;

CARBOMETHOXY GROUPS; CATALYTIC HETEROGENEOUS; DISUBSTITUTED PHENOLS; MONOSUBSTITUTED PHENOLS;

PHENOLS;

EID: 34347270125     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2007.03.001     Document Type: Article

References (27)

1. Besson M., and Pinel C. Top. Catal. 25 (2003) 43-61
2. Kukula P., and Prins R. Top. Catal. 25 (2003) 29-42
3. Ranade V.S., Consiglio G., and Prins R. J. Org. Chem. 64 (1999) 8862
4. Ranade V.S., Consiglio G., and Prins R. J. Org. Chem. 65 (2000) 1132
5. Fache F., Lehuede S., and Lemaire M. Tetrahedron Lett. 36 (1995) 885
6. Besson M., Gallezot P., Neto S., and Pinel C. Chem. Commun. (1998) 1431
7. Besson M., Delbecq F., Gallezot P., Neto S., and Pinel C. Chem. Eur. J. 6 (2000) 949
8. Ranade V.S., and Prins R. J. Catal. 185 (1999) 479
9. Ranade V.S., Consoglio G., and Prins R. Catal. Lett. 58 (1999) 71
10. Hariharan P.C., and Pople J.A. Theor. Chim. Acta 28 (1973) 213
11. Frisch M.J., Trucks G.W., Schlegel H.B., Scuseria G.E., Robb M.A., Cheeseman J.R., Zakrzewski V.G., Montgomery Jr. J.A., Startmann R.E., Burant J.C., Dapprich S., Millam J.M., Daniels A.D., Kudin K.N., Strain M.C., Farkas O., Tomasi J., Barone V., Cossi M., Cammi R., Mennucci B., Pomelli C., Adamo C., Clifford S., Ochterski J., Petersson G.A., Ayala P.Y., Cui Q., Morokuma K., Malick D.K., Rubuck A.D., Raghavachari K., Foresman J.B., Cioslowski J., Oritz J.V., Stefanov B.B., Liu G., Liashenko A., Piskorz P., Komaromi I., Comperts R., Martin R.L., Fox D.J., Keith T., Al-Laham M.A., Peng C.Y., Nanayakkara A., Gonzalez C., Challacombe M., Gill P.M.W., Johnson B., Chen W., Wong M.W., Andres J.L., Gonzalez C., Head-Gordon M., Replogle E.S., and Pople J.A. Gaussian 98, Revision A 6 (1998), Gaussian Inc., Pittsburgh, PA
12. Grev R.S., Janssen C.L., and Schaefer H.F. Chem. Phys. 95 (1991) 5128
13. Eliel E.L., and Wilen S.H. Stereochemistry of Carbon Compounds (1994), John Wiley & Sons Inc. pp. 686-726
14. Two conformers are present when the ester is equatorial and only one when the ester is axial {A figure is presented}
15. Smith G.V., and Notheisz F. Heterogeneous Catalysis in Organic Chemistry (1999), Academic Press (Chapter 1)
16. Linstead R.P., Doering W.E., Davis S.B., Levine P., and Wetstone R.R. J. Am. Chem. Soc. 64 (1942) 1985
17. Siegel S. Adv. Catal. 16 (1966) 123
18. Vavon G. Bull. Soc. Chim. France 4-39 (1926) 668
19. Siegel S., and Smith G.V. J. Am. Chem. Soc. 82 (1960) 6082
20. Burwell R.L., Shim B.K.S., and Rowlinson H.C. J. Am. Chem. Soc. 79 (1957) 5142
21. Sauvage J.F., Baker R.H., and Hussey A.S. J. Am. Chem. Soc. 82 (1960) 6090
22. Smith G.V., and Swoap J.R. J. Org. Chem. 31 (1966) 3904
23. Gault F.G., Rooney J.J., and Kemball C. J. Catal. 1 (1962) 255
24. Besson M., Bullivant L., Nicolaus N., and Gallezot P. J. Catal. 140 (1993) 30
25. Takagi Y., Nishimura S., Taya K., and Hirota K. J. Catal. 8 (1967) 100
26. Takagi Y., Nishimura S., and Hirota K. J. Catal. 12 (1968) 21
27. Allakhverdiev A.I., Kul'kova N.V., and Murzin D.Y. Ind. Eng. Chem. Res. 34 (1995) 1539