Platinum oxide (PtO2): A potent hydrosilylation catalyst

Organic Letters

Volumn 4, Issue 13, 2002, Pages 2117-2119

  Sabourault, Nicolas ^a   Mignani, Gérard ^b   Wagner, Alain ^a   Mioskowski, Charles ^a  

^a UNIVERSITÉ DE STRASBOURG   (France)

^b Rhodia Europe   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE;

EID: 0041877492     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol025658r     Document Type: Article

References (28)

1. (a) Noll, W. Chemistry and Technology of Silicones; Academic Press: New York, 1968; p 437.
2. (b) Eaborn, C.; Bott, R. W. In Organometallic Compounds of the Group IV Elements; MacDiarmid, A. G., Ed.; Dekker: New York, 1968; Vol. 1, p 105.
3. (a) Brook, M. A. Silicon in Organic, Organometallic, and Polymer Chemistry; Wiley: New York, 1999.
4. (b) Marciniec, B.; Gulinski, J.; Urbaniak, W.; Kornetka, Z. W. Comprehensive Handbook on Hydrosilylation; Pergamon: Oxford, 1992.
5. Ojima, I. The Hydrosilylation Reaction. In The Chemistry of Organic Silicon Compounds; Patai, S., Rappoport, Z., Eds.; Wiley: Chichester, U.K., 1989; Vol. 1, Chapter 25, p 1479.
6. Plueddemann, E. D. Silane Coupling Agents; Plenum Press: New York, 1982.
7. (a) Felfoldi, K.; Kapocsi, I.; Bartok, M. J. Organomet. Chem. 1989, 362, 411.
8. (b) For review, see: Brunner, H. Angew. Chem., Int. Ed. Engl. 1983, 22, 897.
9. For review, see also ref 2c.
10. (a) Brockmann, M.; Dieck, H.; Klaus, J. J. Organomet. Chem. 1986, 301, 2091.
11. (b) Chujo, Y.; Ihara, E.; Ihara, H.; Saegusta, T. Macomolecules 1989, 22, 2040.
12. Friedmann, G.; Brossas, J. Polym. Bull. 1983, 10, 28.
13. (a) Fang, T. R.; Kennedy, J. P. Polym. Bull. 1983, 10, 82.
14. (b) Kennedy, J. P.; Carlson, G. M. J. Polym. Sci., Polym. Chem. Ed. 1983, 21, 3551.
15. Friedmann, G.; Herz, J.; Brossas, J. Polym. Bull. 1982, 6, 252.
16. (a) Marciniec, B.; Gulinski, J.; Urbaniak, W.; Nowicka, T.; Mirecki, J. Appl. Organomet. Chem. 1990, 4, 27.
17. (b) Ryan, J. W.; Speier, J. L. J. Org. Chem. 1966, 31, 2698.
18. Coy, D. H.; Fitton, F.; Haszeldine, R. N.; Newslands, M. J.; Tipping, A. E. J. Chem. Soc., Dalton Trans. 1974, 1852.
19. (a) Coy, D. H.; Fitton, F.; Haszeldine, R. N.; Newlands, M. J.; Tipping, A. E. J. Chem. Soc., Dalton Trans. 1974, 1852.
20. (b) Seyferth, D.; Washburne, S. S.; Attridge, C. J.; Yamamoto, K. J. Am. Chem. Soc. 1970, 92, 4405.
21. Seyferth, D.; Prud'homme, C. C.; Wang, W.-L. J. Organomet. Chem. 1984, 277, 203.
22. + - EtOH). Bp = 72°C/ 0.5 mbar.
23. (a) Hitchcock, P. B.; Lappert, M. F.; Warhurst, N. J. W. Angew. Chem., Int. Ed. Engl. 1991, 30, 438.
24. (b) Karstedt, B. D. U.S. Patent 3,-814,720, 1974.
25. Chauhan, M.; Hauck B. J.; Keller L. P.; Boudjouk P. J. Organomet. Chem. 2002, 645, 1.
26. (a) Wagner, G. H. U.S. Patent 2,632,013, 1953.
27. (b) Wagner, G. H. U.S. Patent 2,637,738, 1953.
28. +). Bp = 105°C/26 mmHg.