Effective conversion sucrose into 5-hydroxymethylfurfural by tyrosine in [Emim]Br

Journal of Molecular Catalysis A: Chemical

Volumn 379, Issue , 2013, Pages 350-354

  Su, Kunmei ^a   Liu, Xin ^a   Ding, Min ^a   Yuan, Qiuju ^a   Li, Zhenhuan ^a   Cheng, Bowen ^a  

^a TIANJIN POLYTECHNIC UNIVERSITY   (China)

Author keywords

5 Hydroxymethylfurfural; Amino acids; Biomass conversion; Sucrose; Tyrosine

Indexed keywords

5 HYDROXYMETHYL FURFURALS; BIOMASS CONVERSION; CATALYTIC EFFECTS; CATALYTIC PROCESS; OPTIMAL REACTION CONDITION; POSSIBLE MECHANISMS; REACTION TEMPERATURE; TYROSINE;

AMINO ACIDS; BIOCONVERSION; FRUCTOSE; GLUCOSE; IONIC LIQUIDS;

SUGAR (SUCROSE);

EID: 84884951051     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2013.09.003     Document Type: Article

References (35)

1. Y. Román-Leshkov, J.N. Chheda, and J.A. Dumesic Science 312 2006 1933
2. C. Moreau, M.N. Belgacem, and A. Gandini Top. Catal. 27 2004 11
3. C. Moreau, A. Finiels, and L. Vanoye J. Mol. Catal. A 253 2006 165
4. M.E. Zakrzewska, E. Bogel-Łukasik, and R. Bogel-Łukasik Chem. Rev. 111 2011 397
5. H. Zhao, J.E. Holladay, H. Brown, and Z.C. Zhang Science 316 2007 1597
6. G. Yong, Y. Zhang, and J.Y. Ying Angew. Chem. Int. Ed. 47 2008 9345
7. J.B. Binder, and R.T. Raines J. Am. Chem. Soc. 131 2009 1979
8. S. Lima, P. Neves, M.M. Antunes, M. Pillinger, N. Ignatyev, and A.A. Valente Appl. Catal. A 363 2009 93
9. S. Hu, Z. Zhang, J. Song, X. Zhou, and B. Han Green Chem. 11 2009 1746
10. J.N. Chheda, Y. Román-Leshkov, and J.A. Dumesic Green Chem. 9 2007 342
11. L. Vanoye, M. Fanselow, J.D. Holbrey, M.P. Atkins, and K.S. Seddona Green Chem. 11 2009 390
12. C. Li, Z. Zhang, and Z.K. Zhao Tetrahedron Lett. 50 2009 5403
13. Y. Román-Leshkov, C.J. Barrett, Z.Y. Liu, and J.A. Dumesic Nature 447 2007 982
14. M. Bicker, J. Hirth, and H. Vogel Green Chem. 5 2003 280
15. B.M.F. Kuster Starch 42 1990 314
16. H. Ishida, and K. Seri J. Mol. Catal. A 112 1996 L163
17. S.Q. Hu, Z.F. Zhang, Y.X. Zhou, B.X. Han, H.L. Fan, W.J. Li, J.L. Song, and Y. Xie Green Chem. 10 2008 1280
18. X.H. Qi, M. Watanabe, T.M. Aida, and R.L. Smith Green Chem. 11 2009 1327
19. C. Moreau, R. Durand, S. Razigade, J. Duhamet, P. Faugeras, P. Rivalier, P. Ros, and G. Avignon Appl. Catal. A 145 1996 211
20. X. Qi, M. Watanabe, T.M. Aida, and R.L. Smith Jr. Green Chem. 10 2008 799
21. C. Lansalot-Matras, and C. Moreau Catal. Commun. 4 2003 517
22. V.V. Ordomsky, J. van der Schaaf, J.C. Schouten, and T.A. Nijhuis J. Catal. 287 2012 68
23. J.R. Keeffe, and A.J. Kresge Z. Rappoport, The Chemistry of Enols 1990 Wiley Chichester 399 480
24. K.N. Allen, A. Lavie, G. Farber, A. Glasfeld, G. Petsko, and D. Ringe Biochemistry 33 1994 1481
25. A.Y. Kovalevsky, L. Hanson, S.Z. Fisher, M. Mustyakimov, S.A. Mason, V. Trevor, M.P. Forsyth, D.A. Blakeley, T. Keen, H.L. Wagner, A.K. Carrell, J.P. Katz, P. Glusker, and Langan Structure 18 2010 688
26. M. Moliner, Y. Román-Leshkov, and M.E. Davis Proc. Natl. Acad. Sci. U.S.A. 107 2010 6164
27. Y. Yang, X. Xiang, D. Tong, C. Hu, and M. Abu-Omar Bioresour. Technol. 116 2012 302
28. J.A. Chun, J.W. Lee, Y.B. Yi, S.S. Hong, and Ch.H. Chung Korean J. Chem. Eng. 27 2010 930
29. Y. Tewari Appl. Biochem. Biotechnol. 23 1990 187
30. F.A. Carey Organic Chemistry 4th ed. 2000 McGraw Hill New York, NY
31. M. Marzo, A. Gervasini, and P. Carniti Carbohydr. Res. 347 2012 23
32. K. Beckerle, and J. Okuda J. Mol. Catal. A 356 2012 158
33. W. Liu, Y. Hou, W. Wu, S. Ren, Y. Jing, and B. Zhang Ind. Eng. Chem. Res. 50 2011 6952
34. A. Pinkert, K.N. Marsh, S.S. Pang, and M.P. Staiger Chem. Rev. 109 2009 6712
35. A.A. Rosatella, L.C. Brancob, and C.A.M. Afonso Green Chem. 11 2009 1406