Chirally modified platinum nanoparticles stabilized by dendritic core-multishell architectures for the asymmetric hydrogenation of ethyl pyruvate

Advanced Synthesis and Catalysis

Volumn 352, Issue 9, 2010, Pages 1503-1511

  Keilitz, Juliane ^a   Nowag, Sabrina ^a   Marty, Jean Daniel ^b   Haag, Rainer ^a  

^a FREIE UNIVERSITÄT BERLIN   (Germany)

^b Université Paul Sabatier   (France)

Author keywords

Asymmetric catalysis; Chiral modification; Dendritic; Hydrogenation; Nanoparticles; Recycling

Indexed keywords

EID: 77954249103     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201000128     Document Type: Article

References (44)

1. T. Mallat, A. Baiker, Appl. Catal. A 2000, 200, 3-22.
2. T. Mallat, E. Orglmeister, A. Baiker, Chem. Rev. 2007, 107, 4863-4890.
3. Y. Orito, S. Imai, S. Niwa, J. Chem. Soc. Jpn. 1979, 1118-1120.
4. Y. Orito, S. Imai, S. Niwa, J. Chem. Soc. Jpn. 1980, 670-672.
5. S. Niwa, S. Imai, Y. Orito, J. Chem. Soc. Jpn.1982,137-138.
6. H.-U. Blaser, H.-P. Jalett, M. Müller, M. Studer, Catal. Today 1997, 37, 441-463.
7. M. Von Arx, T. Mallat, A. Baiker, Top. Catal. 2002, 19, 75-87.
8. M. Studer, H.-U. Blaser, C. Exner, Adv. Synth. Catal. 2003,345,45-65.
9. H.-U. Blaser, M. Studer, Acc. Chem. Res. 2007, 40, 1348-1356.
10. T. P. Yoon, E. N. Jacobsen, Science 2003, 299, 1691-1693.
11. K. Kacprzak, J. Gawronski, Synthesis 2001, 7, 961-998.
12. J. L. Margitfalvi, P. Marti, A. Baiker, L. Botz, O. Sticher, Catal. Lett. 1990, 6, 281-288.
13. L. Durán Pachón, G. Rothenberg, Appl. Organomet. Chem. 2008, 22, 288-299.
14. R. M. Crooks, M. Zhao, L. Sun, V. Chechik, L. K. Yeung, Acc. Chem. Res. 2001, 34,181-190.
15. C. Müller, M. G. Nijkamp, D. Vogt, Eur. J. Inorg. Chem. 2005, 4011-4021.
16. D. Astruc, F. Lu, J. R. Aranzaes, Angew. Chem. 2005, 117, 8062-8083;
17. Angew. Chem. Int. Ed. 2005, 44, 7852-7872.
18. P. J. Collier, J. A. Iggo, R. Whyman, J. Mol. Catal. A: Chem. 1999, 146,149-157.
19. J. U. Köhler, J. S. Bradley, Langmuir 1998, 14, 2730-2735.
20. X. Zuo, H. Liu, D. Guo, X. Yang, Tetrahedron 1999, 55, 7787-7804.
21. V. Mevellec, C. Mattioda, J. Schulz, J.-P. Rolland, A. Roucoux, J. Catal. 2004, 225, 1-6.
22. H. Bönnemann, G. A. Braun, Angew. Chem. 1996, 108, 2120-2123;
23. Angew. Chem. Int. Ed. Engl. 1996, 35, 1992-1995.
24. H. P. Dijkstra, G. P. M. van Klink, G. van Koten, Acc. Chem. Res. 2002,35, 798-810.
25. R. Sablong, U. Schlotterbeck, D. Vogt, S. Mecking, Adv. Synth. Catal. 2003,345, 333-336.
26. M. Zhao, R. M. Crooks, Angew. Chem. 1999,111, 375-377;
27. Angew. Chem. Int. Ed. 1999, 38, 364-366.
28. Y. Niu, R. M. Crooks, Comptes Rendus Chimie 2003, 6, 1049-1059.
29. C. C. Tzschucke, C. Markert, W. Bannwarth, S. Roller, A. Hebel, R. Haag, Angew. Chem. 2002, 114, 4136-4173;
30. Angew. Chem. Int. Ed. 2002, 41, 3964-4000.
31. J. Keilitz, M. R. Radowski, J.-D. Marty, R. Haag, F. Gauffre, C. Mingotaud, Chem. Mater. 2008, 20, 2423-2425.
32. -1).
33. 2 pressure, 1 h; modification for 24 h if not otherwise stated.
34. H.-U. Blaser, H.-P. Jalett, M. Garland, M. Studer, H. Thies, A. Wirth-Tijani, J. Catal. 1998, 173, 282-294.
35. J. T. Wehrli, A. Baiker, D. M. Monti, H. U. Blaser, J. Mol. Catal. 1989, 49,195-203.
36. J. T. Wehrli, A. Baiker, D. M. Monti, H. U. Blaser, J. Mol. Catal. 1990, 61, 207-226.
37. -1, water/acetic acid 1:1, S/C/modifier 1000/1/1.5, 70 bar hydrogen pressure, 30 min; modification for 2 h.
38. M. Bartok, T. Bartok, G. Szollosi, K. Felfoldi, Catal. Lett. 1999, 61, 57-60.
39. V. Morawsky, U. Prusse, L. Witte, K. D. Vorlop, Catal. Commun. 2000, 1,15-20.
40. J. U. Köhler, J. S. Bradley, Catal. Lett. 1997, 45, 203-208.
41. X. Zuo, H. Liu, M. Liu, Tetrahedron Lett. 1998, 39, 1941-1944.
42. M. R. Radowski, A. Shukla, H. von Berlepsch, C. Böttcher, G. Pickaert, H. Rehage, R. Haag, Angew. Chem. 2007, 119, 1287-1292;
43. Angew. Chem. Int. Ed. 2007, 46, 1265-1269.
44. S. Küchler, M. R. Radowski, T. Blaschke, M. Dathe, J. Plendl, R. Haag, M. Schäfer-Korting, K. D. Kramer, Eur. J. Pharm. Biopharm. 2009, 71, 243-250.