oa Silica-Supported Palladium-Based Catalysts for Clean Synthesis

References

1. R. F. Heck, Org. React., 1982, 27, 345 [Google Scholar]
2. R. F. Heck, Palladium Reagents in Organic Synthesis”, Academic Press, Orlando, FL, 1985 [Google Scholar]
3. M. Shibasaki, E. M. Vogl, J. Organomet. Chem., 1999, 576, 1 [Google Scholar]
4. N. Miyaura, T. Yanagi, A. Suzuki, Synth. Commun., 1981, 11, 513 [Google Scholar]
5. N. Miyaura, A. Suzuki, Chem. Rev., 1995, 95, 2457 [Google Scholar]
6. A. Suzuki, J. Organomet. Chem., 1999, 576, 147 [Google Scholar]
7. K. Sonogashira, Tetahedron Lett., 1975, 4467 [Google Scholar]
8. P. T. Tanev, T. J. Pinnavaia, Science, 1995, 267, 865 [Google Scholar]
9. M. Laspéras, T. Lloret, L. Chaves, I. Rodriguez, A. Cauvel, D. Brunel, Stud. Surf. Sci. Catal., 1997, 108, 75 [Google Scholar]
10. D. Brunel, Microp. Mesop. Mater., 1999, 27, 329 [Google Scholar]
11. D. J. Macquarrie, Chem. Commun., 1996, 1961 [Google Scholar]
12. D. Macquarrie, D. B. Jackson, J. E. G. Mdoe, J. H. Clark, New J. Chem., 1999, 23, 539 [Google Scholar]
13. J. E. G. Mdoe, J. H. Clark, D. J. Macquarrie, Synlett, 1998, 625 [Google Scholar]
14. D. J. Macquarrie, D. B. Jackson, S. Tailland, K. A. Utting, J. Mater. Chem., 2001, in press [Google Scholar]
15. J. A. Elings, R. Ait-Meddour, J. H. Clark, D. J. Macquarrie, Chem. Commun., 1998, 2707 [Google Scholar]
16. I. C. Chisem, J. Rafelt, M. T. Shieh, J. Chisem, J. H. Clark, R. Jachuck, D. J. Macquarrie, C. Ramshaw, K. Scott, Chem. Commun., 1998, 1949 [Google Scholar]
17. E. B. Mubofu, J. H. Clark, D. J. Macquarrie, Green Chem., 2000, 2, 53 [Google Scholar]
18. A. J. Butterworth, J. H. Clark, P. H. Walton, S. J. Barlow, Chem. Commun., 1996, 1859 [Google Scholar]
19. B. K. Das, J. H. Clark, Chem. Commun., 2000, 605 [Google Scholar]
20. H. E. B. Lempers, R. A. Sheldon, J. Catal., 1998, 175, 62 [Google Scholar]
21. B. B. Wentzel, S.-M. Leinonen, S. Thompson, D. C. Sherrington, M. C. Feiters, R J. M. Nolte, J. Chem. Soc, Perkin Trans. 1, 2000, 3428 [Google Scholar]
22. S. P. Stanforth, Tetrahedron, 1998, 54, 263 [Google Scholar]
23. T. Hayashi, T. Mise, S. Mitachi, K. Yamomoto, M. Kumada, Tetrahedron Lett., 1976, 1133 [Google Scholar]
24. T. Hayashi, A. Yamomoto, T. Hagihara, Y. Ito, Tetrahedron Lett., 1986, 191 [Google Scholar]
25. B. Pugin, European Appl. 729,969; Chem. Abstr., 1996, 125:276188z [Google Scholar]
26. B. Pugin, World Appl. 96/32,400; Chem. Abstr., 1997, 126:8302r [Google Scholar]
27. B. Pugin, World Appl. 97/02,232; Chem. Abstr., 1997, 126:185879e [Google Scholar]
28. W. R. Cullen, N. F. Han, J. Organomet. Chem., 1987, 333, 269 [Google Scholar]
29. B. F. G. Johnson, S. A. Raynor, D. S. Shephard, T. Mashmeyer, J. M. Thomas, G. Sankar, S. Bromley, R. Oldroyd, L. Gladden, M. Mantle, Chem. Commun., 1999, 1167 [Google Scholar]
30. B. Gotov, Š. Toma, D. J. Macquarrie, Enantiomer, 1999, 4, 263 [Google Scholar]
31. B. Gotov, Š. Toma, D. J. Macquarrie, New J. Chem., 2000, 24, 597 [Google Scholar]
32. S. Toma, B. Gotov, J. Cvengroš, D. J. Macquarrie, Chem. Pap., 2001, in press [Google Scholar]
33. D. J. Macquarrie, S. E. Fairfield, J. Mater. Chem., 1997, 7, 2201 [Google Scholar]