Using deep eutectic solvents to improve the resolution of racemic 1-(4-methoxyphenyl)ethanol through Acetobacter sp. CCTCC M209061 cell-mediated asymmetric oxidation

RSC Advances

Volumn 5, Issue 9, 2015, Pages 6357-6364

  Xu, Pei ^a   Cheng, Jing ^a   Lou, Wen Yong ^a   Zong, Min Hua ^a  

^a SOUTH CHINA UNIVERSITY OF TECHNOLOGY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ACETOBACTER; BIOCOMPATIBILITY; CATALYSIS; CELL MEMBRANES; CELLS; ETHANOL; EUTECTICS; ORGANIC SOLVENTS;

AQUEOUS SYSTEM; ASYMMETRIC OXIDATION; CELL MEMBRANE PERMEABILITY; DEEP EUTECTIC SOLVENTS; OPTIMAL CONTENT; REACTION EFFICIENCY; REACTION MEDIA; SUBSTRATE CONCENTRATIONS;

CYTOLOGY;

EID: 84920811591     PISSN: None     EISSN: 20462069     Source Type: Journal    
DOI: 10.1039/c4ra12905a     Document Type: Article

References (27)

1. R. N. Patel, Enzyme Microb. Technol., 2002, 31, 804-826.
2. D. Gamenara and P. Dominguez de Maria, Biotechnol. Adv., 2009, 27, 278-285.
3. M. C. Hillier, J. I. Desrosiers, J. F. Marcoux and E. J. J. Grabowski, Org. Lett., 2004, 6, 573-576.
4. M. C. Hillier, J. F. Marcoux, D. Zhao, E. J. J. Grabowski, A. E. McKeown and R. D. Tillyer, J. Org. Chem., 2005, 70, 8385-8394.
5. R. Wohlgemuth, Curr. Opin. Biotechnol., 2010, 21, 713-724.
6. Y. Ni and J. H. Xu, J. Mol. Catal. B: Enzym., 2002, 18, 233-241.
7. N. S. Hatzakis and I. Smonou, Bioorg. Chem., 2005, 33, 325-337.
8. M. Egi, K. Sugiyama, M. Saneto, R. Hanada, K. Kato and S. Akai, Angew. Chem., Int. Ed., 2013, 52, 3742-3746.
9. Q. H. Zhang, K. De Oliveira Vigier, S. Royer and F. Jerome, Chem. Soc. Rev., 2012, 41, 7108-7146.
10. K. Shahbaz, F. S. Mjalli, M. A. Hashim and I. M. AlNashef, Energy Fuels, 2011, 25, 2671-2678.
11. M. Francisco, A. van den Bruinhorst and M. C. Kroon, Green Chem., 2012, 14, 2153-2157.
12. D. Lloyd, T. Vainikka, L. Murtomäki, K. Kontturi and E. Ahlberg, Electrochim. Acta, 2011, 56, 4942-4948.
13. M. Sharma, C. Mukesh, D. Mondal and K. Prasad, RSC Adv., 2013, 3, 18149-18155.
14. J. T. Gorke, F. Srienc and R. J. Kazlauskas, Chem. Commun., 2008, 1235-1237.
15. H. Zhao, G. A. Baker and S. Holmes, Org. Biomol. Chem., 2011, 9, 1908-1916.
16. H. Zhao, G. A. Baker and S. Holmes, J. Mol. Catal. B: Enzym., 2011, 72, 163-167.
17. D. Lindberg, M. de la Fuente Revenga and M. Widersten, J. Biotechnol., 2010, 147, 169-171.
18. Z. Maugeri and P. Domínguez de María, ChemCatChem, 2014, 6, 1535-1537.
19. B. Singh, H. Lobo and G. Shankarling, Catal. Lett., 2011, 141, 178-182.
20. S. A. Gangu, L. R. Weatherley and A. M. Scurto, Curr. Org. Chem., 2009, 13, 1242-1258.
21. G. de Gonzalo, I. Lavandera, K. Durchschein, D. Wurm, K. Faber and W. Kroutil, Tetrahedron: Asymmetry, 2007, 18, 2541-2546.
22. M. Hayyan, M. A. Hashim, A. Hayyan, M. A. Al-Saadi, I. M. AlNashef, M. E. S. Mirghani and O. K. Saheed, Chemosphere, 2013, 90, 2193-2195.
23. C. J. Bunthof and T. Abee, Appl. Environ. Microbiol., 2002, 68, 2934-2942.
24. Z. J. Xiao, M. H. Zong and W. Y. Lou, Bioresour. Technol., 2009, 100, 5560-5565.
25. X. H. Chen, W. Y. Lou, M. H. Zong and T. J. Smith, BMC Biotechnol., 2011, 11, 110.
26. M. Y. Chang and R. S. Juang, Enzyme Microb. Technol., 2005, 36, 75-82.
27. Ş. A. Çetinus, H. N. Öztop and D. Saraydin, Enzyme Microb. Technol., 2007, 41, 447-454.