A cyclodextrin dimer as a supramolecular reaction platform for aqueous organometallic catalysis

Chemical Communications

Volumn 49, Issue 62, 2013, Pages 6989-6991

  Blaszkiewicz, Claire ^a,c   Bricout, Hervé ^a   Léonard, Estelle ^b   Len, Christophe ^b   Landy, David ^d   Cézard, Christine ^c   Djedaíni Pilard, Florence ^c   Monflier, Eric ^a   Tilloy, Sébastien ^a  

^a UNIVERSITÉ D'ARTOIS   (France)

^b UNIVERSITÉ DE PICARDIE JULES VERNE   (France)

^c UNIVERSITÉ DE TECHNOLOGIE DE COMPIÈGNE   (France)

^d UNIVERSITÉ DU LITTORAL CÔTE D OPALE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; ALKENE; CYCLODEXTRIN; MACROMOLECULE; ORGANOMETALLIC COMPOUND; WATER; ALKENE DERIVATIVE; DIMER;

CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; DIMERIZATION; MACROMOLECULE; MOLECULAR DYNAMICS; SYNTHESIS; ARTICLE; BINDING SITE; CATALYST; HYDROFORMYLATION; HYDROGEN BOND; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STEREOSPECIFICITY; SUPRAMOLECULAR CHEMISTRY;

ALDEHYDES; ALKENES; CATALYSIS; CYCLODEXTRINS; DIMERIZATION; MACROMOLECULAR SUBSTANCES; MOLECULAR DYNAMICS SIMULATION; MOLECULAR STRUCTURE; ORGANOMETALLIC COMPOUNDS; WATER;

EID: 84882245624     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c3cc43647k     Document Type: Article

References (48)

1. P. W. N. M. van Leeuwen, Supramolecular Catalysis, Wiley-VCH, Weinheim, 2008
2. M. J. Wilkinson, P. W. N. M. van Leeuwen, J. N. H. Reek, Org. Biomol. Chem. 2005, 3, 2371.
3. B. Breit, Angew. Chem. Int. Ed. 2005, 44, 6816.
4. D. M. Vriezema, M. C. Aragonès, J. A. A. W. Elemans, J. J. L. M. Cornelissen, A. E. Rowan, R. J. M. Nolte, Chem. Rev. 2005, 105, 1445.
5. A. Lützen, Angew. Chem. Int. Ed. 2005, 44, 1000.
6. D. Fiedler, D. H. Leung, R. G. Bergman, K. N. Raymond, Acc. Chem. Res. 2005, 38, 351.
7. T. S. Koblenz, J. Wassenaar, J. N. H. Reek, Chem. Soc. Rev. 2008, 37, 247.
8. M. Yoshizawa, J. K. Klosterman, M. Fujita, Angew. Chem. Int. Ed. 2009, 48, 3418.
9. J. Meeuwissen, J. N. H. Reek, Nat. Chem. 2010, 2, 615.
10. S. Carboni, C. Gennari, L. Pignataro, U. Piarulli, Dalton Trans. 2011, 40, 4355.
11. T. R. Ward, Acc. Chem. Res. 2011, 44, 47.
12. M. L. Merlau, M. Del Pilar Mejia, S. T. Nguyen, J. T. Hupp, Angew. Chem. Int. Ed. 2001, 40, 4239.
13. B. Breit, W. Seiche, J. Am. Chem. Soc. 2003, 125, 6608.
14. V. F. Slagt, M. Röder, P. C. J. Kamer, P. W. N. M. van Leeuwen, J. N. H. Reek, J. Am. Chem. Soc. 2004, 126, 4056.
15. X. B. Jiang, L. Lefort, P. E. Goudriaan, A. H. M. de Vries, P. W. N. M. van Leeuwen, J. G. de Vries, J. N. H. Reek, Angew. Chem. Int. Ed. 2006, 45, 1223.
16. S. Das, C. D. Incarvito, R. H. Crabtree, G. W. Brudvig, Science, 2006, 312, 1941.
17. M. Yoshizawa, M. Tamura, M. Fujita, Science, 2006, 312, 251.
18. H. Gulys, J. Benet-Buchholz, E. C. Escudero-Adan, Z. Freixa, P. W. N. M. van Leeuwen, Chem. Eur. J. 2007, 13, 3424.
19. T. Šmejkal, B. Breit, Angew. Chem. Int. Ed. 2008, 47, 311.
20. S. Zhu, J. V. Ruppel, H. Lu, L. Wojtas, X. P. Zhang, J. Am. Chem. Soc. 2008, 130, 5042.
21. L. Diab, T. Šmejkal, J. Geier, B. Breit, Angew. Chem. Int. Ed. 2009, 48, 8022.
22. L. Pignataro, B. Lynikaite, J. Cvengros, M. Marchini, U. Piarulli, C. Gennari, Eur. J. Org. Chem. 2009, 2539.
23. H. J. Yoon, J. Kuwabara, J. H. Kim, C. A. Mirkin, Science, 2010, 330, 66.
24. P. Dydio, W. I. Dzik, M. Lutz, B. de Bruin, J. N. H. Reek, Angew. Chem. Int. Ed. 2011, 50, 396.
25. P. Dydio, C. Rubay, T. Gadzikwa, M. Lutz, J. N. H. Reek, J. Am. Chem. Soc. 2011, 133, 17176.
26. H. Yamaguchi, T. Hirano, H. Kiminami, D. Taura, A. Harada, Org. Biomol. Chem. 2006, 4, 3571.
27. C. Machut, J. Patrigeon, S. Tilloy, H. Bricout, F. Hapiot, E. Monflier, Angew. Chem. Int. Ed. 2007, 46, 3040.
28. P. J. Deuss, G. Popa, C. H. Botting, W. Laan, P. C. J. Kamer, Angew. Chem. Int. Ed. 2010, 49, 5315.
29. C. J. Brown, G. M. Miller, M. W. Johnson, R. G. Bergman, K. N. Raymond, J. Am. Chem. Soc. 2011, 133, 11964.
30. J. W. Steed and J. L. Atwood, Supramolecular Chemistry, Wiley, Chichester, 2000
31. R. Breslow, L. E. Overman, J. Am. Chem. Soc. 1970, 92, 1075.
32. R. Breslow, B. Zhang, J. Am. Chem. Soc. 1992, 114, 5882.
33. R. Breslow, B. Zhang, J. Am. Chem. Soc. 1994, 116, 7893.
34. R. Breslow, Acc. Chem. Res. 1995, 28, 146.
35. R. Breslow, X. Zhang, R. Xu, M. Maletic, R. Merger, J. Am. Chem. Soc. 1996, 118, 11678.
36. R. Breslow, X. Zhang, Y. Huang, J. Am. Chem. Soc. 1997, 119, 4535.
37. R. Breslow, B. Zhang, J. Am. Chem. Soc. 1997, 119, 1676.
38. R. Breslow, S. D. Dong, Chem. Rev. 1998, 98, 1997.
39. J. Yang, R. Breslow, Angew. Chem. Int. Ed. 2000, 39, 2692.
40. J. Yang, B. Gabriele, S. Belvedere, Y. Huang, R. Breslow, J. Org. Chem. 2002, 67, 5057.
41. R. Breslow, J. M. Yan, S. Belvedere, Tetrahedron Lett. 2002, 43, 363.
42. Z. Fang, R. Breslow, Bioorg. Med. Chem. Lett. 2005, 15, 5463.
43. M. Ferreira, H. Bricout, F. Hapiot, A. Sayede, S. Tilloy, E. Monflier, Chem Sus Chem, 2008, 1, 631.
44. K. A. Connors, Binding Constants, Wiley, New York, 1987
45. E. G. Kuntz, CHEMTECH, 1987, 570.
46. E. G. Kuntz, Rhône-Poulenc, French Patent, 2366237, 1976
47. R. Gärtner, B. Cornils, H. Springer and P. Lappe, DE Pat, 3235030, 1982
48. F. Hapiot, L. Leclercq, N. Azaroual, S. Fourmentin, S. Tilloy, E. Monflier, Curr. Org. Synth. 2008, 5, 162.