Palladium supported on an ion exchange resin for the Suzuki-Miyaura reaction

Cuihua Xuebao/Chinese Journal of Catalysis

Volumn 34, Issue 12, 2013, Pages 2161-2166

  Zhang, Mingming ^a   Jiang, Manman ^a   Liang, Changhai ^a  

^a DALIAN UNIVERSITY OF TECHNOLOGY   (China)

Author keywords

Anion exchange resin; Bifunctional catalyst; Metal organic chemical vapor deposition; Palladium; Suzuki Miyaura coupling reaction

Indexed keywords

AEROBIC CONDITION; AMBERLITE IRA-900; ANION EXCHANGE RESINS; BI-FUNCTIONAL CATALYSTS; METAL-ORGANIC; PHENYLBORONIC ACIDS; SUZUKI-MIYAURA COUPLING REACTION; SUZUKI-MIYAURA REACTION;

CATALYST ACTIVITY; ION EXCHANGE RESINS; LOADING; METALLORGANIC CHEMICAL VAPOR DEPOSITION; ORGANIC ACIDS; PALLADIUM; ULTRAVIOLET VISIBLE SPECTROSCOPY; VAPORS;

CHEMICAL REACTIONS;

EID: 84890104351     PISSN: 02539837     EISSN: None     Source Type: Journal    
DOI: 10.1016/s1872-2067(12)60698-6     Document Type: Article

References (30)

1. Yin L, Liebscher J. Chem Rev, 2007, 107: 133
2. Garrett C E, Prasad K. Adv Synth Catal, 2004, 346: 889
3. Welch C J, Albaneze-Walker J, Leonard W R, Biba M, DaSilva J, Henderson D, Laing B, Mathre D J, Spencer S, Bu X, Wang T. Org Process Res Dev, 2005, 9: 198
4. Zapf A, Beller M. Top Catal, 2002, 19: 101
5. Baumeister P, Meyer W, Oertle K, Seifert G, Steiner H. Chimia, 1997, 51: 144
6. Blaser H U, Indolese A, Schnyder A, Steiner H, Studer M. J Mol Catal A, 2001, 173: 3
7. Zhao F, Bhanage B M, Shirai M, Arai M. Chem Eur J, 2000, 6: 843
8. Hagiwara H, Shimizu Y, Hoshi T, Suzuki T, Ando M, Okubo K, Yokoyama C. Tetrahedron Lett, 2001, 42: 4349
9. Toebes M L, van Dillen J A, de Jong K P. J Mol Catal A, 2001, 173: 75
10. Mehnert C P, Weaver D W, Ying J Y. J Am Chem Soc, 1998, 120: 12289
11. Djakovitch L, Koehler K. J Am Chem Soc, 2001, 123: 5990
12. Djakovitch L, Koehler K. J Mol Catal A, 1999, 142: 275
13. Biffis A, Zecca M, Basato M. Eur J Inorg Chem, 2011: 1131
14. Wagner M, Köhler K, Djakovitch L, Weinkauf S, Hagen V, Muhler M. Top Catal, 2000, 13: 319
15. Köhler K, Wagner M, Djakovitch L. Catal Today, 2001, 66: 105
16. Li J, Mau A W H, Strauss C R. Chem Commun, 1997: 1275
17. Zhang M, Guan J, Zhang B, Su D, Williams C T, Liang C. Catal Lett, 2012, 142: 313
18. Djakovitch L, Wagner M, Hartung C G, Beller M, Koehler K. J Mol Catal A, 2004, 219: 121
19. Corain B, Zecca M, Canton P, Centomo P. Phil Trans R Soc A, 2010, 368: 1495
20. Seki T, Grunwaldt J D, Baiker A. Chem Commun, 2007: 3562
21. Seki T, Grunwaldt J D, van Vegten N, Baiker A. Adv Synth Catal, 2008, 350: 691
22. Laufer W, Hoelderich W F. Chem Commun, 2002: 1684
23. Laufer W, Niederer J P M, Hoelderich W F. Adv Synth Catal, 2002, 344: 1084
24. Roveda A, Benedetti A, Pinna F, Strukul G. Inorg Chim Acta, 2003, 349: 203
25. Gasparovicova D, Kralik M, Hronec M, Biffis A, Zecca M, Corain B. J Mol Catal A, 2006, 244: 258
26. Xiang D, Liu X F, Sun J S, Xiao F S, Sun J M. Catal Today, 2009, 148: 383
27. Dent W T, Long R, Wilkinson A J. J Chem Soc, 1964: 1585
28. Shaw B L. Proc Chem Soc, 1960: 247
29. Gasparovicova D, Kralik M, Hronec M, Vallusova Z, Vinek H, Corain B. J Mol Catal A, 2007, 264: 93
30. Neyertz C, Marchesini F A, Boix A, Miro E, Querini C A. Appl Catal A, 2010, 372: 40