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Kurt Faber

O.Univ.-Prof. Univ.-Doz. Dr.phil.

1988 …2016
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Epoxide Hydrolases Chemical Compounds
Cyclization Chemical Compounds
Epoxy Compounds Chemical Compounds
Alkenes Chemical Compounds
Hydrolysis Chemical Compounds
Substrates Chemical Compounds
Enzymes Chemical Compounds
Acetogenins Chemical Compounds

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Research Output 1988 2016

Chemo-, regio- and stereoselectivity of carboxylic acid reductases

Winkler, C. K., Plank, M., Winkler, M. & Faber, K., 30 Aug 2016.

Research output: Contribution to conferencePosterResearch

Stereocontrol strategies in the asymmetric bioreduction of alkenes

Oberdorfer, G., Gruber, K., Faber, K. & Hall, M., 23 Jul 2012, In : Synlett. 23, 13, p. 1857-1864 8 p.

Research output: Contribution to journalArticleResearchpeer-review

Alkenes
Substrates
Oxidoreductases
Stereoselectivity
Enantiomers

Catalophore: Mining of structural databases using 3D-templates

Steinkellner, G., Gruber, C., Pavkov-Keller, T., Lyskowski, A. F., Schwamberger, O., Steiner, K., Winkler, C., Schwab, H., Faber, K. & Gruber, K., 2011.

Research output: Contribution to conferencePosterResearch

Identification of two enone-reductases by database mining using 3D active site templates

Steinkellner, G., Gruber, C., Pavkov-Keller, T., Lyskowski, A. F., Schwamberger, O., Steiner, K., Winkler, C., Schwab, H., Faber, K. & Gruber, K., 2011.

Research output: Contribution to conferencePosterResearch

Stereopreferences of old yellow enzymes: Structure correlations and sequence patterns in enoate reductases

Oberdorfer, G., Steinkellner, G., Stueckler, C., Faber, K. & Gruber, K., 17 Oct 2011, In : ChemCatChem. 3, 10, p. 1562-1566 5 p.

Research output: Contribution to journalArticleResearchpeer-review