The first heterogeneous carbonylative Sonogashira coupling reaction catalyzed by MCM-41-supported bidentate phosphine palladium(0) complex

Journal of Molecular Catalysis A: Chemical

Volumn 298, Issue 1-2, 2009, Pages 94-98

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

^a JIANGXI NORMAL UNIVERSITY   (China)

Author keywords

Bidentate phosphine ligand; Carbonylative Sonogashira coupling reaction; Heterogeneous catalysis; MCM 41; Supported palladium catalyst

Indexed keywords

ACETYLENE; ATMOSPHERIC PRESSURE; CARBON MONOXIDE; CATALYSIS; CATALYSTS; HYDROCARBONS; LIGANDS; PALLADIUM; PHOSPHORUS COMPOUNDS;

BIDENTATE PHOSPHINE LIGAND; CARBONYLATIVE SONOGASHIRA COUPLING REACTION; HETEROGENEOUS CATALYSIS; MCM-41; SUPPORTED PALLADIUM CATALYST;

PALLADIUM COMPOUNDS;

EID: 58049213793     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2008.09.031     Document Type: Article

References (38)

1. Chowdhury C., and Kundu N.G. Tetrahedron 55 (1999) 7011 and references therein
2. Dodero V.I., Koll L.C., Faraoni M.B., Mitchell T.N., and Podesta J.C. J. Org. Chem. 68 (2003) 10087
3. Vong B.G., Kim S.H., Abraham S., and Theodorakis E.A. Angew. Chem. Int. Edit. 43 (2004) 3947
4. Trost B.M., and Ball Z.T. J. Am. Chem. Soc. 126 (2004) 13942
5. Trost B.M., and Schmidt T. J. Am. Chem. Soc. 110 (1988) 2301
6. Kel'in A.V., Sromek A.W., and Gevorgyan V. J. Am. Chem. Soc. 123 (2001 2074)
7. Sheng H., Lin S., and Huang Y. Tetrahedron Lett. 27 (1986) 4893
8. Kel'in A.V., and Gevorgyan V. J. Org. Chem. 67 (2002) 95
9. Davis R.B., and Scheiber D.H. J. Am. Chem. Soc. 78 (1956) 1675
10. Logue M.W., and Moore G.L. J. Org. Chem. 40 (1975) 131
11. Schmit U., and Schwochau M. Chem. Ber. 97 (1964) 1649
12. Vereshchagin L.I., Yashina O.G., and Zarva T.V. Zh. Org. Khim. 2 (1966) 1895
13. Walton D.R.M., and Waugh F. J. Organomet. Chem. 37 (1972) 45
14. Logue M.W., and Teng K. J. Org. Chem. 47 (1982) 2549
15. Goure W.F., Wright M.E., Davis P.D., Labadie S.S., and Stille J.K. J. Am. Chem. Soc. 106 (1984) 6417
16. Grisp G.T., Scott W.J., and Stille J.K. J. Am. Chem. Soc. 106 (1984) 7500
17. Arcadi A., Cacchi S., Marinelli F., Pace P., and Sanzi G. Synlett (1995) 823
18. Mohamed Ahmed M.S., and Mori A. Org. Lett. 5 (2003) 3057
19. Liang B., Huang M., You Z., Xiong Z., Lu K., Fathi R., Chen J., and Yang Z. J. Org. Chem. 70 (2005) 6097
20. de Miguel Y.R. J. Chem. Soc., Perkin Trans. 1 (2000) 4213
21. Shuttleworth S.J., Allin S.M., Wilson R.D., and Nasturica D. Synthesis (2000) 1035
22. Loch J.A., and Crabtree R.H. Pure Appl. Chem. 73 (2001) 119
23. Corain B., and Kralik M. J. Mol. Catal. A: Chem. 173 (2001) 99
24. Yin L., and Liebscher J. Chem. Rev. 107 (2007) 133
25. Kresge C.T., Leonowicz M.E., Roth W.J., Vartuli J.C., and Beck J.S. Nature 359 (1992) 710
26. 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
27. 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
28. Maschmeyer T., Rey F., Sankar G., and Thomas J.M. Nature 378 (1995) 159
29. Liu C.-J., Li S.-G., Pang W.-Q., and Che C.-M. Chem. Commun. (1997) 65
30. Mehnert P.C., Weaver D.W., and Ying J.Y. J. Am. Chem. Soc. 120 (1998) 12289
31. Zhou J.M., Zhou R.X., Mo L.Y., Zhao S.F., and Zheng X.M. J. Mol. Catal. A: Chem. 178 (2002) 289
32. Mukhopadhyay K., Sarkar B.R., and Chaudhari R.V. J. Am. Chem. Soc. 124 (2002) 9692
33. Yang H., Zhang G., Hong X., and Zhu Y. J. Mol. Catal. A: Chem. 210 (2004) 143
34. Cai M., Xu Q., and Sha J. J. Mol. Catal. A: Chem. 272 (2007) 293
35. Lim M.H., and Stein A. Chem. Mater. 11 (1999) 3285
36. Arya P., Panda G., Rao N.V., Alper H., Bourque S.C., and Manzer L.E. J. Am. Chem. Soc. 123 (2001) 2889
37. Hudkins C.M.G., Knights K.A., Johnson B.F.G., de Miguel Y.R., Raja R., and Thomas J.M. Chem. Commun. (2001) 2624
38. Kayaki Y., Shimokawatoko Y., and Ikariya T. Adv. Synth. Catal. 345 (2003) 175