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chemistry (41) 41
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organic chemistry (19) 19
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acyclic, carbocyclic or heterocyclic compounds containingelements other than carbon, hydrogen, halogen, oxygen, nitrogen,sulfur, selenium or tellurium (15) 15
beer (15) 15
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1. Full Text Nicotinamide-independent asymmetric bioreduction of C{double bond, long}C-bonds via disproportionation of enones catalyzed by enoate reductases
by Stueckler, Clemens and Reiter, Tamara C and Baudendistel, Nina and Faber, Kurt
Tetrahedron, ISSN 0040-4020, 01/2010, Volume 66, Issue 3, pp. 663 - 667
Disproportionation | Flavin | Cofactor recycling | Enoate reductase | Biotransformation | Fundamental and applied biological sciences. Psychology | Bioconversions. Hemisynthesis | Organic chemistry | Biotechnology | Chemistry | Kinetics and mechanisms | Methods. Procedures. Technologies | Reactivity and mechanisms | Exact sciences and technology | Biological and medical sciences
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2. Full Text Asymmetric Synthesis of (R)‐3‐Hydroxy‐2‐methylpropanoate (‘Roche Ester’) and Derivatives via Biocatalytic CC‐Bond Reduction
by Stueckler, Clemens and Winkler, Christoph K and Bonnekessel, Melanie and Faber, Kurt
Advanced synthesis & catalysis, ISSN 1615-4150, 10/2010, Volume 352, Issue 14‐15, pp. 2663 - 2666
old yellow enzyme | CC‐bioreduction | enoate reductase | substrate engineering | biocatalysis | C=C-bioreduction | Physical Sciences | Chemistry | Chemistry, Organic | Chemistry, Applied | Science & Technology
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3. Full Text Asymmetric Bioreduction of Activated Alkenes Using Cloned 12‐Oxophytodienoate Reductase Isoenzymes OPR‐1 and OPR‐3 from Lycopersicon esculentum (Tomato): A Striking Change of Stereoselectivity
by Hall, Mélanie and Stueckler, Clemens and Kroutil, Wolfgang and Macheroux, Peter and Faber, Kurt
Angewandte Chemie (International ed.), ISSN 1433-7851, 05/2007, Volume 46, Issue 21, pp. 3934 - 3937
oxidoreductases | enzymes | asymmetric catalysis | reduction | carbonyl compounds | Carbonyl compounds | Enzymes | Reduction | Oxidoreductases | Asymmetric catalysis | Oxidation-Reduction | Aldehydes - chemical synthesis | Stereoisomerism | Carboxylic Acids - chemical synthesis | Imides - chemical synthesis | Lycopersicon esculentum - enzymology | Isoenzymes - chemistry | Oxidoreductases - chemistry | Oxidoreductases Acting on CH-CH Group Donors - chemistry | Alkenes - chemistry | Lactones - chemical synthesis | Imides - chemistry | Arabidopsis Proteins - chemistry | Ketones - chemical synthesis | Carboxylic Acids - chemistry | Ketones - chemistry | Molecular Structure | Aldehydes - chemistry | Lactones - chemistry | Index Medicus
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4. Full Text Stereopreferences of Old Yellow Enzymes: Structure Correlations and Sequence Patterns in Enoate Reductases
by Oberdorfer, Gustav and Steinkellner, Georg and Stueckler, Clemens and Faber, Kurt and Gruber, Karl
ChemCatChem, ISSN 1867-3880, 10/2011, Volume 3, Issue 10, pp. 1562 - 1566
enzymes | sequence motifs | structure–activity relationships | stereospecificity | biocatalysis | Sequence motifs | Enzymes | Stereospecificity | Biocatalysis | Structure-activity relationships | Physical Sciences | Chemistry | Chemistry, Physical | Science & Technology
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5. Full Text Stereocomplementary Bioreduction of α,β-Unsaturated Dicarboxylic Acids and Dimethyl Esters using Enoate Reductases:  Enzyme- and Substrate-Based Stereocontrol
by Stueckler, Clemens and Hall, Mélanie and Ehammer, Heidemarie and Pointner, Eva and Kroutil, Wolfgang and Macheroux, Peter and Faber, Kurt
Organic letters, ISSN 1523-7060, 12/2007, Volume 9, Issue 26, pp. 5409 - 5411
Dicarboxylic Acids - chemistry | NAD - chemistry | Esters - chemistry | Stereoisomerism | Glucose - chemistry | Substrate Specificity | NADP - chemistry | Oxidoreductases - chemistry | Index Medicus
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6. Full Text Asymmetric Bioreduction of CC Bonds using Enoate Reductases OPR1, OPR3 and YqjM: Enzyme‐Based Stereocontrol
by Hall, Mélanie and Stueckler, Clemens and Ehammer, Heidemarie and Pointner, Eva and Oberdorfer, Gustav and Gruber, Karl and Hauer, Bernard and Stuermer, Rainer and Kroutil, Wolfgang and Macheroux, Peter and Faber, Kurt
Advanced synthesis & catalysis, ISSN 1615-4150, 02/2008, Volume 350, Issue 3, pp. 411 - 418
stereocomplementary process | old yellow enzyme | asymmetric bioreduction | enoate reductase | nitroalkenes | α,β‐unsaturated carbonyl compounds | Asymmetric bioreduction | Old yellow enzyme | Enoate reductase | α,β-unsaturated carbonyl compounds | Nitroalkenes | Stereocomplementary process | Physical Sciences | Chemistry | Chemistry, Organic | Chemistry, Applied | Science & Technology
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7. Full Text Development of a Continuous Flow Process for a Matteson Reaction: From Lab Scale to Full-Scale Production of a Pharmaceutical Intermediate
by Stueckler, Clemens and Hermsen, Peter and Ritzen, Bas and Vasiloiu, Maria and Poechlauer, Peter and Steinhofer, Stefan and Pelz, Andreas and Zinganell, Christopher and Felfer, Ulfried and Boyer, Serge and Goldbach, Michel and de Vries, André and Pabst, Thomas and Winkler, Georg and LaVopa, Vito and Hecker, Scott and Schuster, Christian
Organic process research & development, ISSN 1083-6160, 05/2019, Volume 23, Issue 5, pp. 1069 - 1077
Physical Sciences | Chemistry | Chemistry, Organic | Chemistry, Applied | Science & Technology
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8. Full Text Asymmetric Synthesis of O‐Protected Acyloins Using Enoate Reductases: Stereochemical Control through Protecting Group Modification
by Winkler, Christoph K and Stueckler, Clemens and Mueller, Nicole J and Pressnitz, Desiree and Faber, Kurt
11/2010, Volume 2010, Issue 33, 5
Enzymes | Reduction | Biocatalysis | Asymmetric synthesis | Enones | Physical Sciences | Chemistry | Chemistry, Organic | Science & Technology | Alicyclic compounds, terpenoids, prostaglandins, steroids | Organic chemistry | Alicyclic compounds | Preparations and properties | Exact sciences and technology
Book Review
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9. Full Text Stereo‐Controlled Asymmetric Bioreduction of α,β‐Dehydroamino Acid Derivatives
by Stueckler, Clemens and Winkler, Christoph K and Hall, Mélanie and Hauer, Bernhard and Bonnekessel, Melanie and Zangger, Klaus and Faber, Kurt
Advanced synthesis & catalysis, ISSN 1615-4150, 05/2011, Volume 353, Issue 7, pp. 1169 - 1173
old yellow enzyme | asymmetric bioreduction | ene‐reductase | dehydroamino acids | stereocontrol | ene-reductase | Physical Sciences | Chemistry | Chemistry, Organic | Chemistry, Applied | Science & Technology | Fundamental and applied biological sciences. Psychology | Bioconversions. Hemisynthesis | Organic chemistry | Biotechnology | Methods. Procedures. Technologies | Exact sciences and technology | Biological and medical sciences | Preparations and properties | Aliphatic compounds
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10. Full Text The Substrate Spectra of Pentaerythritol Tetranitrate Reductase, Morphinone Reductase, N‐Ethylmaleimide Reductase and Estrogen‐Binding Protein in the Asymmetric Bioreduction of Activated Alkenes
by Mueller, Nicole J and Stueckler, Clemens and Hauer, Bernhard and Baudendistel, Nina and Housden, Hazel and Bruce, Neil C and Faber, Kurt
Advanced synthesis & catalysis, ISSN 1615-4150, 02/2010, Volume 352, Issue 2‐3, pp. 387 - 394
enoate reductase | NEM reductase | biotransformations | estrogen‐binding protein | alkene bioreduction | PETN reductase | morphinone reductase | Estrogen-binding protein | Enoate reductase | Alkene bioreduction | Biotransformations | Morphinone reductase | Physical Sciences | Chemistry | Chemistry, Organic | Chemistry, Applied | Science & Technology
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11. Full Text Cover Picture: Stereopreferences of Old Yellow Enzymes: Structure Correlations and Sequence Patterns in Enoate Reductases (ChemCatChem 10/2011)
by Oberdorfer, Gustav and Steinkellner, Georg and Stueckler, Clemens and Faber, Kurt and Gruber, Karl
ChemCatChem, ISSN 1867-3880, 10/2011, Volume 3, Issue 10, pp. 1513 - 1513
Journal Article
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12. Full Text Nicotinamide-independent asymmetric bioreduction of CC-bonds via disproportionation of enones catalyzed by enoate reductases
by Stueckler, Clemens and Reiter, Tamara C and Baudendistel, Nina and Faber, Kurt
Tetrahedron, ISSN 0040-4020, 01/2010, Volume 66, Issue 3-2, pp. 663 - 667
Journal Article
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13. Full Text Nicotinamide-independent asymmetric bioreduction of CC-bonds via disproportionation of enones catalyzed by enoate reductases
by Stueckler, Clemens and Reiter, Tamara C and Baudendistel, Nina and Faber, Kurt
Tetrahedron, ISSN 0040-4020, 01/2010, Volume 66, Issue 3, pp. 663 - 667
Flavin | Disproportionation | Cofactor recycling | Enoate reductase | Biotransformation | Niacinamide | Oxidoreductases
Journal Article
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14. Full Text Clemens Intert und Emily Fink sind Tennis-Landesmeister
by Ulrich Stuckler
Hamburger Abendblatt, 02/2013
Newspaper Article
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15. Full Text Asymmetric Bioreduction of Activated Alkenes Using Cloned 12-Oxophytodienoate Reductase Isoenzymes OPR-1 and OPR-3 fromLycopersicon esculentum (Tomato): A Striking Change of Stereoselectivity
by Hall, Mélanie and Stueckler, Clemens and Kroutil, Wolfgang and Macheroux, Peter and Faber, Kurt
Angewandte Chemie (International ed.), ISSN 1433-7851, 05/2007, Volume 46, Issue 21, pp. 3934 - 3937
Journal Article
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16. Full Text Bioreduction of α-methylcinnamaldehyde derivatives: chemo-enzymatic asymmetric synthesis of Lilial™ and Helional™Electronic supplementary information (ESI) available: general experimental conditions, source of substrates, synthesis of reference compounds, spectroscopic data of substrates and products, and analytical procedures for the determination of conversion and enantiomeric excess of products. See DOI: 10.1039/c002971h
by Stueckler, Clemens and Mueller, Nicole J and Winkler, Christoph K and Glueck, Silvia M and Gruber, Karl and Steinkellner, Georg and Faber, Kurt
ISSN 1477-9226, 8/2010, Volume 39, Issue 36, pp. 8472 - 8476
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17. Full Text Asymmetric Bioreduction of Activated C=C Bonds Using Zymomonas mobilis NCR Enoate Reductase and Old Yellow Enzymes OYE 1–3 from Yeasts
by Hall, Mélanie and Stueckler, Clemens and Hauer, Bernhard and Stuermer, Rainer and Friedrich, Thomas and Breuer, Michael and Kroutil, Wolfgang and Faber, Kurt
03/2008, Volume 2008, Issue 9, 6
Old Yellow Enzymes | Enzymes | Reduction | Alkenes | Nitroalkenes | Stereocontrol | Old yellow enzymes | Physical Sciences | Chemistry | Chemistry, Organic | Science & Technology
Book Review
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