W. Stampfer

发表

Modeling the chromatographic enantioseparation of aryl- and hetarylcarbinols on ULMO, a brush-type chiral stationary phase, by 3D-QSAR techniques.

W. Fabian, M. Mazur, G. Uray, 2003, Chirality.

Regio‐ and Stereoselective Reduction of Diketones and Oxidation of Diols by Biocatalytic Hydrogen Transfer

W. Kroutil, K. Faber, Klaus Edegger, 2006 .

Purification and characterization of a chemotolerant alcohol dehydrogenase applicable to coupled redox reactions

W. Goessler, W. Kroutil, K. Faber, 2004, Biotechnology and bioengineering.

Preparation of an epoxide-hydrolyzing biocatalyst: Rhodococcus ruber DSM 44540—an activity-growth study

S. M. Glueck, W. Kroutil, K. Faber, 2002 .

Efficient production of raspberry ketone via 'green' biocatalytic oxidation

R. V. Deursen, W. Kroutil, K. Faber, 2003 .

Biocatalytic asymmetric hydrogen transfer employing Rhodococcus ruber DSM 44541.

W. Kroutil, K. Faber, W. Stampfer, 2003, The Journal of organic chemistry.

Biocatalytic asymmetric hydrogen transfer.

C. Moitzi, W. Kroutil, K. Faber, 2002, Angewandte Chemie.

Optimization of the organic solvent-stable asymmetric hydrogen transfer system of Rhodococcus ruber DSM 44541: an activity-growth study

S. M. Glueck, W. Kroutil, K. Faber, 2003 .

Chemo- and stereo-selective biocatalytic reduction of α,β-unsaturated ketones employing a chemo-tolerant ADH from Rhodococcus ruber DSM 44541

R. V. Deursen, W. Kroutil, K. Faber, 2004 .

On the organic solvent and thermostability of the biocatalytic redox system of Rhodococcus ruber DSM 44541

W. Kroutil, K. Faber, W. Stampfer, 2003, Biotechnology and bioengineering.

Selectivity enhancement of epoxide hydrolase catalyzed resolution of 2,2-disubstituted oxiranes by substrate modification

Kurt Faber, Ingrid Osprian, K. Faber, 2000 .

Comparison of Chirasil-DEX CB as gas chromatographic and ULMO as liquid chromatographic chiral stationary phase for enantioseparation of aryl- and heteroarylcarbinols.

W. Fabian, G. Uray, W. Stampfer, 2003, Journal of chromatography. A.

Simple Biocatalytic Access to Enantiopure (S)‐1‐Heteroarylethanols Employing a Microbial Hydrogen Transfer Reaction

W. Kroutil, K. Faber, Klaus Edegger, 2004 .

Biocatalytic oxidative kinetic resolution of sec-alcohols: stereocontrol through substrate-modification

W. Kroutil, K. Faber, W. Stampfer, 2003 .

Practical and Large-Scale Synthesis of rac-(3S,4aR,10aR) -6-Methoxy-1-propyl-1,2,3,4,4a,5,10,10a-octahydrobenzo [g]quinoline-3-carboxylic Acid Methyl Ester.

W. Stampfer, M. Baenziger, U. Sunay, 2001 .