1 |
Katzman, M. A. (2009) Current considerations in the treatment of generalized anxiety disorder. Adis International LTD, New Zealand. CNS Drugs 23: 103-120.
DOI
ScienceOn
|
2 |
Glieder, A., R. Weis, W.Skranc, P. Poechlauer, I. Dreveny, S. Majer, M. Wubbolts, H. Schwab, and K. Gruber (2003) Comprehensive step-by-step engineering of an (R)-hydroxynitrile lyase for large-scale asymmetric synthesis. Angew. Chem. Int. Ed. 42: 4815-4818.
DOI
ScienceOn
|
3 |
Sun, Y., X. Wan, J. Wang, Q. Meng, H. Zhang, L. Jiang, and Z. Zhang (2005) Ru-catalyzed asymmetric hydrogenation of -Ketoesters with CeCl3․7H2O as additive. Org. Lett. 7: 5425-5427.
DOI
ScienceOn
|
4 |
Uhm, K ., S. Lee, H . Kim, H . Kang, and Y. Lee (2007) Enantioselective resolution of methyl 2-chloromandelate by candida antarctica lipase A in a solvent-free transesterification reaction. J. Mol. Catal. B. Enzym. 45: 34-38.
DOI
ScienceOn
|
5 |
de Souza Pereira, R. (1998) The use of baker's yeast in the generation of asymmetric centers to produce chiral drugs and other compounds. Crit. Rev. Biotechnol. 18: 25-83.
DOI
ScienceOn
|
6 |
van Langen, L. M., R. P. Selassa, F. van Rantwijk, and R. A. Sheldon (2005) Cross-linked aggregates of (R)-oxynitrilase: a stable, recyclable biocatalyst for enantioselective hydrocyanation. Org. Lett. 7: 327-329.
DOI
ScienceOn
|
7 |
Johanson, T., M. Carlquist, C. Olsson, A. Rudolf, T. Frejd, and M. F. Gorwa-Grauslund (2008) Reaction and strain engineering for improved stereo-selective whole-cell reduction of a bicyclic diketone. Appl. Microbiol. Biotechnol. 77: 1111-1118.
DOI
ScienceOn
|
8 |
Katz, M., I. Sarvary, T. Frejd, B. Hahn-Hagerdal, and M. F. Gorwa-Grauslund (2002) An improved stereoselective reduction of a bicyclic diketone by Saccharomyces cerevisiae combining process optimization and strain engineering. Appl. Microbiol. Biotechnol. 59: 641-648.
DOI
ScienceOn
|
9 |
Li, G., K. Huang, Y. Jiang, and P. Ding (2007) Production of (R)-mandelic acid by immobilized cells of Saccharomyces cerevisiae on chitosan carrier. Process Biochem. 42: 1465-1469.
DOI
ScienceOn
|