Enantioselective reduction of α-Cyano and α-Nitro substituted acetophenones promoted by a bifunctional mesoporous silica

ChemCatChem

Volumn 5, Issue 10, 2013, Pages 2856-2860

  Deng, Boxin ^a   Cheng, Tanyu ^a   Wu, Meng ^a   Wang, Jinyu ^a   Liu, Guohua ^a  

^a SHANGHAI NORMAL UNIVERSITY   (China)

Author keywords

Asymmetric catalysis; Bifunctional catalysis; Heterogeneous catalyst; Immobilization; Mesoporous material

Indexed keywords

ASYMMETRIC CATALYSIS; BIFUNCTIONAL CATALYSIS; CETYL TRIMETHYL AMMONIUM BROMIDES; ENANTIOSELECTIVE REDUCTION; FUNCTIONALIZED; HETEROGENEOUS CATALYST; MESOPOROUS SILICA; SYNERGISTIC EFFECT;

CATALYSIS; ENANTIOSELECTIVITY; KETONES; RADIOACTIVE WASTE VITRIFICATION;

MESOPOROUS MATERIALS;

EID: 84884939947     PISSN: 18673880     EISSN: 18673899     Source Type: Journal    
DOI: 10.1002/cctc.201300340     Document Type: Article

References (31)

1. C. E. Song, Handbook of Asymmetric Heterogeneous Catalysis (Eds.: K.L. Ding, Y. Uozumi), Wiley-VCH, Weinheim, 2009, pp.25;
2. P. J. Walsh, H. M. Li, C. A. deParrodi, Chem. Rev. 2007, 107, 2503;
3. M. Heitbaum, F. Glorius, I. Escher, Angew. Chem. 2006, 118, 4850; Angew. Chem. Int. Ed. 2006, 45, 4732;
4. Z. Wang, G. Chen, K. L. Ding, Chem. Rev. 2009, 109, 322;
5. M. Bartók, Chem. Rev. 2010, 110, 1663;
6. A. Bartoszewicz, N. Ahlsten, B. Martín-Matute, Chem. Eur. J. 2013, 19, 7274.
7. C. Li, H. D. Zhang, D. M. Jiang, Q. H. Yang, Chem. Commun. 2007, 547;
8. H. Q. Yang, L. Zhang, L. Zhong, Q. H. Yang, C. Li, Angew. Chem. 2007, 119, 6985; Angew. Chem. Int. Ed. 2007, 46, 6861;
9. S. Y. Bai, H. Q. Yang, P. Wang, J. S. Gao, B. Li, Q. H. Yang, C. Li, Chem. Commun. 2010, 46, 8145;
10. Y. Shen, Q. Chen, L.-L. Lou, K. Yu, F. Ding, S. Liu, Catal. Lett. 2010, 137, 104.
11. J. M. Thomas, R. Raja, Acc. Chem. Res. 2008, 41, 708;
12. M. D. Jones, R. Raja, J. M. Tohomas, B. F. G. Johnson, D. W. Lewis, J. Rouzaud, K. D. M. Harris, Angew. Chem. 2003, 115, 4462; Angew. Chem. Int. Ed. 2003, 42, 4326.
13. H. J. Zhang, Z. Y. Li, P. P. Xu, R. F. Wu, Z. Jiao, Chem. Commun. 2010, 46, 6783.
14. L. Zhang, Y. N. Guo, J. Peng, X. Liu, P. Yuan, Q. H. Yang, C. Li, Chem. Commun. 2011, 47, 4087.
15. S. Tang, R. H. Jin, H. S. Zhang, H. Yao, J. L. Zhuang, G. H. Liu, H. X. Li, Chem. Commun. 2012, 48, 6286;
16. H. S. Zhang, R. H. Jin, H. Yao, S. Tang, J. L. Zhuang, G. H. Liu, H. X. Li, Chem. Commun. 2012, 48, 7874;
17. W. Xiao, R. H. Jin, T. Y. Cheng, D. Q. Xia, H. Yao, F. Gao, B. X. Deng, G. H. Liu, Chem. Commun. 2012, 48, 11898;
18. D.Q. Xia, T.Y. Cheng, W. Xiao, K.T. Liu, Z.L. Wang, G.H. Liu, H.L. Li, W. Wang, ChemCatChem- 2013, DOI:.
19. Y. Q. Sun, G. H. Liu, H. Y. Gu, T. Z. Huang, Y. L. Zhang, H. X. Li, Chem. Commun. 2011, 47, 2583;
20. J. Long, G. H. Liu, T. Y. Cheng, H. Yao, Q. Q. Qian, J. L. Zhuang, F. Gao, H. X. Li, J. Catal. 2013, 298, 41.
21. O. Soltani, M. A. Ariger, H. Vázquez-Villa, E. M. Carreira, Org. Lett. 2010, 12, 2893;
22. H. Vázquez-Villa, S. Reber, M. A. Ariger, E. M. Carreira, Angew. Chem. 2011, 123, 9141; Angew. Chem. Int. Ed. 2011, 50, 8979;
23. R. terHalle, E. Schulz, M. Lemaire, Synlett 1997, 1257.
24. Y. L. Huang, S. Xu, V. S. Y. Lin, Angew. Chem. 2011, 123, 687; Angew. Chem. Int. Ed. 2011, 50, 661.
25. S. Hiraoka, M. Shiro, M. Shionoya, J. Am. Chem. Soc. 2004, 126, 1214.
26. S. Ogo, N. Makihara, Y. Watanabe, Organometallics 1999, 18, 5470.
27. V. Cauda, A. Schlossbauer, J. Kecht, A. Zürner, T. Bein, J. Am. Chem. Soc. 2009, 131, 11361.
28. P. F. W. Simon, R. Ulrich, H. W. Spiess, U. Wiesner, Chem. Mater. 2001, 13, 3464.
29. O. Kröcher, O. A. Köppel, M. Fröba, A. Baiker, J. Catal. 1998, 178, 284.
30. D. Moon, J. Lee, Langmuir 2012, 28, 12341;
31. C. Wang, Y. Zhou, M. Y. Ge, X. B. Xu, Z. L. Zhang, J. Z. Jiang, J. Am. Chem. Soc. 2010, 132, 46.