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Volumn 15, Issue 10, 1999, Pages 3557-3562

Immobilization of a ligand-preserved giant palladium cluster on a metal oxide surface and its nobel heterogeneous catalysis for oxidation of allylic alcohols in the presence of molecular oxygen

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; ALDEHYDES; ATOMS; CATALYSIS; ELECTRONIC STRUCTURE; HYDROCARBONS; OXIDATION; OXYGEN; SCANNING ELECTRON MICROSCOPY; SURFACES; TITANIUM OXIDES;

EID: 0032653476     PISSN: 07437463     EISSN: None     Source Type: Journal    
DOI: 10.1021/la981720a     Document Type: Article
Times cited : (66)

References (52)
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    • Generally, many metal catalysts could promote oxidations of both allylic and benzyl alcohols. For examples, see: (a) Harding, K. E.; May, L. M.; Dick, K. F. J. Org. Chem. 1975, 40, 1664. (b) Barton, D. H. R.; Kitchin, J. P.; Motherwell, W. B. J. Chem. Soc., Chem. Commun. 1978, 1099. (c) Hirano, M.; Morimoto, T.; Itoh, K. Bull. Chem. Soc. Jpn. 1988, 61, 3749. (d) Muzart, J.; Ajjou, A. N'A.; Ait-Mohand, S. Tetrahedron Lett. 1994, 35, 1989. (e) Lenz, R.; Ley, S. V. J. Chem. Soc., Perkin Trans. 1997, 1, 3291. (f) Markó, I. E.; Giles, P. R.; Tsukazaki, M.; Chellé- Regnaut, I.; Urch, C. J.; Brown, S. M. J. Am. Chem. Soc. 1997, 119, 12661.
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    • Generally, many metal catalysts could promote oxidations of both allylic and benzyl alcohols. For examples, see: (a) Harding, K. E.; May, L. M.; Dick, K. F. J. Org. Chem. 1975, 40, 1664. (b) Barton, D. H. R.; Kitchin, J. P.; Motherwell, W. B. J. Chem. Soc., Chem. Commun. 1978, 1099. (c) Hirano, M.; Morimoto, T.; Itoh, K. Bull. Chem. Soc. Jpn. 1988, 61, 3749. (d) Muzart, J.; Ajjou, A. N'A.; Ait-Mohand, S. Tetrahedron Lett. 1994, 35, 1989. (e) Lenz, R.; Ley, S. V. J. Chem. Soc., Perkin Trans. 1997, 1, 3291. (f) Markó, I. E.; Giles, P. R.; Tsukazaki, M.; Chellé-Regnaut, I.; Urch, C. J.; Brown, S. M. J. Am. Chem. Soc. 1997, 119, 12661.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 12661
    • Markó, I.E.1    Giles, P.R.2    Tsukazaki, M.3    Chellé-Regnaut, I.4    Urch, C.J.5    Brown, S.M.6
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    • note
    • a is as follows: 4,7-dimethyl-phen > 2,9-dimethyl-phen > 5,6-dimethyl-phen > 5-methyl-phen > phen.
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    • Che, M.1    Bennett, C.O.2


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