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Abstrakty
Pd(II) complexes with aminophosphine-based PNP and PCP pincer type ligands were used as catalysts of Heck coupling of bromobenzenes and styrene at 110 graduate C. The best results were obtained with catalyst I, [Pd(PNP-Ph)Cl]Cl, where PNP = N,N'-bis(diphenyl - phosphino)-2,6-diaminopyridine. Heck reaction performed in the presence of I and [Bu4N]Br as co-catalyst produced in 5 h up to 100% of coupling products with E/Z ratio equal from 8.6 to 33.5. Palladium catalyst I was recycled and used at least 3 times with out remark able decrease of catalytic activity.
Słowa kluczowe
Wydawca
Czasopismo
Rocznik
Tom
Strony
1687--1687
Opis fizyczny
–1694, Bibliogr. 27 poz., rys.
Twórcy
autor
autor
autor
autor
autor
- nstitute of Applied Synthetic Chemistry Vienna University of Technology, Getreidemarkt 9, A-1060 Vi enna, Austria, ania@wchuwr.chem.uni.wroc.pl
Bibliografia
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- 2. Dahlhoff W.V. and Nelson S.M.,.J Chem. Soc. (41,2184(1971).
- 3. Albrecht M. and Van Koten G., Angew. Chem., Angew. Chem. Int. Ed., 40, 3750 (2001).
- 4. van der Boom M.E. and Milstein D., Chem. Rev, 103, 1759 (2003).
- 5. Singleton J.T, Tetrahedron, 59, 1837 (2003).
- 6. Beletskaya I.P. and Cheprakov A.P., J. Organomet. Chem., 689, 4055 (2004).
- 7. Heck R.F., J. Am. Chem. Soc., 90, 5518 (1968).
- 8. Jeffrey T, in: Liebeskind L.S. (Ed.), Advances in Metal-Organic Chemistry, Vol. 5, Jai Press Inc, Greenwich, CT, 1996.
- 9. Beletskaya I.P. and Cheprakov A.V., Chem. Rev., 100, 3009 (2000).
- 10. Tucker C.E. and de Vries J.G., Topics in Catalysis, 19, 111 (2002).
- ll. Ohff M., Ohff A., van der Boom M.E. and Milstein D., J. Am. Chem. Soc., 119, 11687(1997).
- 12. Beletskaya I.P., Chuchurjukin A.V., Dijkstra H.P., van Klink G.P.M. and Van Koten G., Tetrahedron Lett.,41, 1075 (2000).
- 13. Morales-Morales D., Cramer R.E. and Jensen C.M., J. Organomet. Chem., 654, 44 (2002).
- 14. Sjóvall S., Wendt O.F. and Andersen C., J. Chem. Soc., Dalton Trans., 1396 (2002).
- 15. Naghipour A., Sabounchei S.J., Morales-Morales D., Hernandez-Ortega S. and Jensen C.M., J. Organomet. Chem., 689, 2494 (2004).
- 16. Kiewel K., Liu Y.S., Bergbreiter D.E. and Sulikowski G.A., Tetrahedron Lett., 40, 8945 (1999).
- 17. Beller M.A. and Zapf A., Synlett, 792 (1998).
- 18. Miyazaki R, Yamaguchi K. and Shibasaki M., Tetrahedron Lett., 40, 7379 (1999).
- 19. Morales-Morales D., Grause C., Kasaoka K., Redón R., Cramer R.E. and Jensen C.M., Inorg. Chim. Acta, 300-302, 958 (2000).
- 20. Morales-Morales D., Redón R„ Yung C. and Jensen C.M., Chem. Commun., 1619 (2000).
- 21. Chanthateyanonth R. and Alper H., J. Mol. Catal. A, 201, 23 (2003).
- 22. Trzeciak A.M. and Ziółkowski J.J., Coord. Chem. Rev„ 249, 2308 (2005).
- 23. Eberhard M.R., Org. Lett., 6, 2125 (2004).
- 24. Sommer WJ., Yu K., Sears J.S., Ji Y, Zhang X., Davis R.J., Sherrill C.D., Jones C.W. and Weck M., Organomet., 124, 4351 (2005).
- 25. Benito-Garagorri D., Becker E., Wiedermann J., Lackner W., Pollak M., Mereiter K., Kisala J. and Kirchner K., Organomet., 125, 1900 (2006).
- 26. Benito-Garagorri D., Bocokič V., Mereiter K. and Kirchner K., Organomet., 125, 3817 (2006).
- 27. Pryjomska-Ray L, Trzeciak A.M. and Ziółkowski J.J., J. Mol. Catal A: Chem., 257, 3 (2006).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ5-0022-0127