Bulky triarylarsines are effective ligands for palladium catalysed Heck olefination

Dalton Transactions

Volumn , Issue 8, 2005, Pages 1491-1498

  Baber, R Angharad ^a   Collard, Simon ^b   Hooper, Mark ^b   Orpen, A Guy ^a   Pringle, Paul G ^a   Wilkinson, Matthew J ^a   Wingad, Richard L ^a  

^a UNIVERSITY OF BRISTOL   (United Kingdom)

^b JOHNSON MATTHEY TECHNOLOGY CENTRE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; CHEMICAL BONDS; INFRARED SPECTROSCOPY; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PALLADIUM; PARAMETER ESTIMATION; STEREOCHEMISTRY;

BOND LENGTHS; COMPLEXES; LIGANDS; REAGENTS;

CHEMICAL REACTIONS;

EID: 18144409140     PISSN: 14779226     EISSN: None     Source Type: Journal    
DOI: 10.1039/b417910b     Document Type: Article

References (36)

1. (a) R. F. Heck, J. Am. Chem. Soc., 1968, 90, 5518;
2. (b) R. F. Heck, J. Am. Chem. Soc., 1971, 93, 6896;
3. (c) J. Tsuji, Acc. Chem. Res., 1969, 2, 151.
4. J. G. deVries, Can. J. Chem., 2001, 79, 1086, and references therein.
5. W. A. Herrmann, C. Brossmer, K. Öfele, C. P. Reisinger, T. Priermeier, M. Beller and H. Fischer, Angew. Chem., Int. Ed. Engl., 1995, 34, 1844.
6. (a) Applied Homogeneous Catalysis with Organometallic Compounds, ed. B. Cornils and W. A. Herrmann, VCH, Weinheim, 1996;
7. (b) W. A. Herrmann, V. P. W. Böhm and C. P. Reisinger, J. Organomet. Chem., 1999, 576, 23;
8. (c) A. Zapf and M. Beller, Top. Catal., 2002, 19, 101.
9. M. Ohff, A. Ohff, M. E. van der Boom and D. Milstein, J. Am. Chem. Soc., 1997, 119, 11687.
10. D. A. Albisson, R. B. Bedford, S. E. Lawrence and P. N. Scully, Tetrahedron Lett., 1998, 39, 9793.
11. S. Gibson, D. F. Foster, R. P. Tooze and D. J. Cole-Hamilton, Chem. Commun., 2001, 779.
12. V. Farina and G. P. Roth in Advances in Metal-Organic Chemistry, ed. L. S. Liebskind, JAI Press, New York, 1996, vol. 5.
13. (a) A. Kojima, C. D. L. Boden and M. Shibasaki, Tetrahedron Lett., 1997, 38, 3459;
14. (b) S. Y. Cho and M. Shibasaki, Tetrahedron Lett., 1998, 39, 1773.
15. (a) G. J. Burrows and E. E. Turner, J. Chem. Soc., 1920, 1373;
16. (b) J. A. S. Howell, M. G. Palin, P. C. Yates, P. McCardle, D. Cunningham, Z. Goldschmidt, H. E. Gottlieb and D. Hezroni-Langeman, J. Chem. Soc., Perkin Trans. 2, 1992, 1772.
17. R. A. Baber, A. G. Orpen, P. G. Pringle, M. J. Wilkinson and R. L. Wingad, Dalton Trans., 2005, 659, and references therein.
18. (a) S. A. Dias and E. C. Alyea, Transition Met. Chem., 1979, 4, 205;
19. (b) E. C. Alyea, G. Ferguson, J. Malito and B. L. Ruhl, Can. J. Chem., 1988, 66, 3162.
20. W. A. Herrmann, C. Brossmer, C. P. Reisinger, T. H. Riermeier, K. Öfele and M. Beller, Chem. Eur. J., 1997, 3, 1357.
21. (a) J.A. Osborn, F. H. Jardine, J. F. Young and G. Wilkinson, J. Chem. Soc. A, 1966, 1711;
22. (b) J. T. Mague and G. Wilkinson, J. Chem. Soc. A, 1966, 1736.
23. J. T. Carlock, Tetrahedron, 1984, 40, 185.
24. L. A. van der Veen, P. K. Keveen, P. C. J. Kamer and P. W. N. M. van Leeuwen, Chem. Commun., 2000, 333.
25. C. A. Tolman, Coord. Chem. Rev., 1977, 77, 313.
26. V. P. W. Böhm and W. A. Herrmann, Chem. Eur. J., 2001, 7, 4191.
27. (a) B. L. Shaw, New J. Chem., 1998, 77;
28. (b) B. L. Shaw, S. D. Perera and E. A. Staley, Chem. Commun., 1998, 1361.
29. (a) A. H. M. de Vries, J. M. C. A. Mulders, J. H. M. Mommers, H. J. W. Henderickx and J. G. de Vries, Org. Lett., 2003, 5, 3285;
30. (b) M. R. Eberhard, Org. Lett., 2004, 6, 2125.
31. A. Biffis, M. Zecca and M. Basato, Eur. J. Inorg. Chem., 2001, 1131.
32. A. B. Pangborn, M. A. Giardello, R. H. Grubbs, R. K. Rosen and F. J. Timmers, Organometallics, 1996, 15, 1518.
33. (a) H. Konishi, K. Aritomi, T. Okano and J. Kiji, Bull. Chem. Soc. Jpn., 1989, 62, 591;
34. (b) N. J. Hales, H. Heeney, J. H. Holinshead and S. V. Ley, Tetrahedron, 1995, 51, 7741.
35. D. Fraccarollo, R. Beitani, M. Mozzon, U. Belluco and R. A. Michelin, Inorg. Chim. Acta., 1992, 201, 15.
36. J. R. Doyle, P. E. Slade and H. B. Jonassen, Inorg. Synth., 1960, 6, 218.