MCM-41-supported bidentate phosphine palladium(II) complex as an efficient catalyst for the carbonylation of aryl halides

Catalysis Communications

Volumn 10, Issue 2, 2008, Pages 257-260

  Hao, Wenyan ^a   Sha, Junchao ^a   Sheng, Shouri ^a   Cai, Mingzhong ^a  

^a JIANGXI NORMAL UNIVERSITY   (China)

Author keywords

Aryl halides; Bidentate phosphine palladium complex; Carbonylation; MCM 41; Supported palladium catalyst

Indexed keywords

ABS RESINS; AMINES; ATMOSPHERIC PRESSURE; CARBON MONOXIDE; CARBONYLATION; CATALYSIS; CATALYSTS; MODEMS; ORGANIC COMPOUNDS; PALLADIUM; PALLADIUM COMPOUNDS; PHOSPHORUS COMPOUNDS; ZEOLITES;

ARYL HALIDES; BIDENTATE PHOSPHINE PALLADIUM COMPLEX; BIDENTATE PHOSPHINES; EFFICIENT CATALYSTS; MCM-41; PALLADIUM CATALYSTS; PALLADIUM COMPLEXES; SUPPORTED PALLADIUM CATALYST;

CATALYST SUPPORTS;

EID: 54049151092     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2008.09.004     Document Type: Article

References (35)

1. For a review, see:. In: Anastas P.T., and Williamson T.C. (Eds). Green Chemistry. ACS Symposium Series vol. 626 (1996), American Chemical Society, Washington, DC and references therein
2. Valentine Jr. D., Tilley J.W., and LeMahieu R.A. J. Org. Chem. 46 (1981) 4614
3. Grushin V.V., and Alper H. J. Chem. Soc., Chem. Commun. (1992) 611
4. Beletskaya I.P., Lapidus A.L., and Petrovskii K.B. Russ. J. Org. Chem. 34 (1998) 1464
5. Lin Y.S., and Yamamoto A. J. Organomet. Chem. 645 (2002) 152
6. Schoenberg A., Bartoletti I., and Heck R.F. J. Org. Chem. 39 (1974) 3318
7. Ben-David Y., Portnoy M., and Milstein D. J. Am. Chem. Soc. 111 (1989) 8742
8. Yang J., Haynes A., and Maitlis P.M. Chem. Commun. 2 (1999) 179
9. Calo V., Giannoccaro P., Nacci A., and Monopoli A. Tetrahedron Lett. 42 (2001) 3299
10. Magerlein W., Beller M., and Indolese A.F. J. Mol. Catal. A 156 (2000) 213
11. Schoenberg A., and Heck R.F. J. Org. Chem. 39 (1974) 3327
12. Perry R.J., and Wilson B.D. Organometallics 13 (1994) 3346
13. Takahashi T., Inoue H., Tomida S., Doi T., and Bray A.M. Tetrahedron Lett. 40 (1999) 7843
14. Magerlein W., Indolese A.F., and Beller M. J. Organomet. Chem. 641 (2002) 30
15. Sakakura T., Claisupakitsin M., Hayashi T., and Tanaka M. J. Organomet. Chem. 334 (1987) 205
16. Ben-David Y., Portnoy M., and Milstein D. J. Chem. Soc., Chem. Commun. (1989) 1816
17. Okano T., Harada N., and Kiji J. Bull. Chem. Soc. Jpn. 67 (1994) 2329
18. Stille J.K. Pure Appl. Chem. 57 (1985) 1771
19. de Miguel Y.R. J. Chem. Soc., Perkin Trans. 1 (2000) 4213
20. Trost B.M., and Warner R.W. J. Am. Chem. Soc. 104 (1982) 6112
21. Khan S.I., and Grinstaff M.W. J. Org. Chem. 64 (1999) 1077
22. Akiyama R., and Kobayashi S. Angew. Chem. Int. Ed. 40 (2001) 3469
23. McNamara C.A., Dixon M.J., and Bradley M. Chem. Rev. 102 (2002) 3275
24. Li P.H., and Wang L. Adv. Synth. Catal. 348 (2006) 681
25. Reddy N.P., Kantam M.L., and Choudary B.M. Ind. J. Chem. 28B (1989) 105
26. Cai M.Z., Song C.S., and Huang X. J. Chem. Soc., Perkin Trans. 1 (1997) 2273
27. Cai M.Z., Zhou J., Zhao H., and Song C.S. React. Funct. Polym. 50 (2002) 191
28. Cai M.Z., Huang Y.Z., Hu R.H., and Song C.S. J. Mol. Catal. A: Chem. 208 (2004) 17
29. Kresge C.T., Leonowicz M.E., Roth W.J., Vartuli J.C., and Beck J.S. Nature 359 (1992) 710
30. Beck J.S., Vartuli J.C., Roth W.J., Leonowicz M.E., Kresge C.T., Schmitt K.D., Chu C.T.-W., Olson D.H., Sheppard E.W., McCullen S.B., Higgins J.B., and Schlenker J.L. J. Am. Chem. Soc. 114 (1992) 10834
31. Zhou W., Thomas J.M., Shephard D.S., Johnson B.F.G., Ozkaya D., Maschmeyer T., Bell R.G., and Ge Q. Science 280 (1998) 705
32. Mehnert P.C., Weaver D.W., and Ying J.Y. J. Am. Chem. Soc. 120 (1998) 12289
33. Yang H., Zhang G., Hong X., and Zhu Y. J. Mol. Catal. A: Chem. 210 (2004) 143
34. Mukhopadhyay K., Sarkar B.R., and Chaudhari R.V. J. Am. Chem. Soc. 124 (2002) 9692
35. Cai M., Sha J., and Xu Q. Tetrahedron 63 (2007) 4642