In situ generation of highly active dissolved palladium species from solid catalysts - A concept for the activation of aryl chlorides in the heck reaction

Angewandte Chemie - International Edition

Volumn 43, Issue 14, 2004, Pages 1881-1882

  Pröckl, Sandra S ^a   Kleist, Wolfgang ^a   Gruber, Markus A ^a   Köhler, Klaus ^a  

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

Aryl chlorides; C C coupling; Heck reactions; Heterogeneous catalysis; Palladium

Indexed keywords

CATALYSTS; CHLORIDE MINERALS; IN SITU COMBUSTION; LEACHING; ZEOLITES;

ARYL CHLORIDES; HECK REACTION; REDEPOSITION;

PALLADIUM COMPOUNDS;

CHLORINE DERIVATIVE; METAL OXIDE; PALLADIUM; ZEOLITE;

ARTICLE; CATALYSIS; CATALYST; CHEMICAL STRUCTURE; HECK REACTION; LEACHING;

EID: 3142613268     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200353473     Document Type: Article

References (24)

1. a) I. P. Beletskaya, A. V. Cheprakov, Chem. Rev. 2000, 100, 3009-3066;
2. b) A. Biffis, M. Zecca, M. Basato, J. Mol. Catal. A 2001, 173, 249-274.
3. M. T. Reetz, E. Westermann, R. Lohmer, G. Lohmer, Tetrahedron Lett. 1998, 39, 8449-8452.
4. a) A. H. M. de Vries, F. J. Parlevliet, L. Schmieder van der Vondervoort, J. H. M. Mommers, H. J. W. Henderickx, M. A. M. Walet, J. G. de Vries, Adv. Synth. Catal. 2002, 344, 996-1002;
5. b) J. G. de Vries, A. H. M. de Vries, Eur. J. Org. Chem. 2003, 799-811;
6. c) A. H. M. de Vries, J. M. C. A. Mulders, J. H. M. Mommers, H. J. W. Henderickx, J. G. de Vries, Org. Lett. 2003, 5, 3285-3288.
7. d) R. G. Heidenreich, J. G. E. Krauter, J. Pietsch, K. Köhler, J. Mol. Catal. A 2892,182-183, 499-509.
8. A. Zapf, M. Beller, Top. Catal. 2002, 19, 101-109.
9. a) A. F. Littke, G. C. Fu, Angew. Chem. 2002, 114, 4350-4386; Angew. Chem. Int. Ed. 2002, 41, 4176-4211;
10. a) A. F. Littke, G. C. Fu, Angew. Chem. 2002, 114, 4350-4386; Angew. Chem. Int. Ed. 2002, 41, 4176-4211;
11. b) M. R. Buchmeiser, K. Wurst, J. Am. Chem. Soc. 1999, 121, 11101-11107;
12. c) M. T. Reetz, G. Lohmer, Chem. Commun. 1996, 1921-1922;
13. d) M. T. Reetz, G. Lohmer, R. Schwickardi, Angew. Chem. 1998, 110, 492-494; Angew. Chem. Int. Ed. 1998, 37, 481-483.
14. d) M. T. Reetz, G. Lohmer, R. Schwickardi, Angew. Chem. 1998, 110, 492-494; Angew. Chem. Int. Ed. 1998, 37, 481-483.
15. a) W. Pearlman, Tetrahedron Lett. 1967, 17, 1663-1664;
16. b) L. Djakovitch, H. Heise, K. Köhler, J. Organomet. Chem. 1999, 584, 16-26;
17. b) S. Fessi, A. Ghorbel, J. Sol-Gel Sci. Technol. 2000, 19, 417-420.
18. a) A. Biffis, M. Zecca, M. Basato, Eur. J. Inorg. Chem. 2001, 1131-1133;
19. b) A. F. Shmidt, L. V. Mametova, Kinet. Catal. 1996, 37, 406-408;
20. c) K. Köhler, R. G. Heidenreich, J. G. E. Krauter, J. Pietsch, Chem. Eur. J. 2002, 8, 622-631.
21. a) R. Srivastava, N. Venkatathri, D. Srinivas, P. Ratnasamy, Tetrahedron Lett. 2003, 44, 3649-3651.
22. b) C. P. Mehnert, D. W. Weaver, J. Y. Ying, J. Am. Chem. Soc. 1998, 120, 12289-12296.
23. a) L. Djakovitch, K. Köhler, J. Am. Chem. Soc. 2001,725, 5990-5999;
24. b) L. Djakovitch, H. Heise, K. Köhler, J. Organomet. Chem. 1999, 584, 16-26.