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Nitrile hydrolysis activity of Rhodococcus erythropolis NCIMB 11540 whole cells.
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- Biotechnology Journal, 2006, v. 1, n. 5, p. 569, doi. 10.1002/biot.200600028
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- Article
On the Mechanism of Oxidation of Non-Phenolic Lignin Model Compounds by the Laccase-ABTS Couple.
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- Holzforschung: International Journal of the Biology, Chemistry, Physics, & Technology of Wood, 1992, v. 46, n. 2, p. 121
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- Article
Glyoxylates as Versatile Building Blocks for the Synthesis of α-Amino Acid and α-Alkoxy Acid Derivatives via Cationic Intermediates.
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- European Journal of Organic Chemistry, 2003, v. 2003, n. 14, p. 2519, doi. 10.1002/ejoc.200200714
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Biokatalytische einstufige Alkenspaltung von Arylalkenen: ein enzymatisches Äquivalent zur reduktiven OzonisierungDieses Projekt wird vom Österreichischen Wissenschaftsfonds (FWF-Projekt P18381) finanziert. Grundlegende Experimente wurden...
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- Angewandte Chemie, 2006, v. 118, n. 31, p. 5325, doi. 10.1002/ange.200601574
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Intramolecular Staudinger Ligation: A Powerful Ring-Closure Method To Form Medium-Sized LactamsWe thank Dr. P. Kamer (Department of Homogeneous Catalysis, University of Amsterdam) for helpful advice and discussions. Dr. A. Van Loevezijn and Ing. C. Salomons (Solvay Pharmaceuticals, Weesp, The Netherlands) are gratefully acknowledged for measuring the LC/ESI-MS spectra. This research has been supported financially by the Council for Chemical Sciences of the Netherlands Organization for Scientific Research (CW-NWO).
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- Angewandte Chemie, 2003, v. 115, n. 36, p. 4509, doi. 10.1002/ange.200351930
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- Article
Chiral Induction Effects in Ruthenium( II) Amino Alcohol Catalysed Asymmetric Transfer Hydrogenation of Ketones: An Experimental and Theoretical Approach.
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- Chemistry - A European Journal, 2000, v. 6, n. 15, p. 2818, doi. 10.1002/1521-3765(20000804)6:15<2818::AID-CHEM2818>3.0.CO;2-Q
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Biocatalytic Single-Step Alkene Cleavage from Aryl Alkenes: An Enzymatic Equivalent to Reductive OzonizationThis study was financed by the Austrian Science Fund (FWF Project P18381). Initial experiments were performed within the Research Centre Applied Biocatalysis supported by DSM, FFG, SFG, Province of Styria and City of Graz.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 31, p. 5201, doi. 10.1002/anie.200601574
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- Article
Intramolecular Staudinger Ligation: A Powerful Ring-Closure Method To Form Medium-Sized LactamsWe thank Dr. P. Kamer (Department of Homogeneous Catalysis, University of Amsterdam) for helpful advice and discussions. Dr. A. Van Loevezijn and Ing. C. Salomons (Solvay Pharmaceuticals, Weesp, The Netherlands) are gratefully acknowledged for measuring the LC/ESI-MS spectra. This research has been supported financially by the Council for Chemical Sciences of the Netherlands Organization for Scientific Research (CW-NWO).
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- Angewandte Chemie International Edition, 2003, v. 42, n. 36, p. 4373, doi. 10.1002/anie.200351930
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- Article
Synthesis of Versatile Building Blocks through Asymmetric Hydrogenation of Functionalized Itaconic Acid Mono‐Esters.
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- Advanced Synthesis & Catalysis, 2008, v. 350, n. 1, p. 85, doi. 10.1002/adsc.200700307
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- Article
Improvement of an Acid Phosphatase/DHAP-Dependent Aldolase Cascade Reaction by Using Directed Evolution.
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- ChemBioChem, 2009, v. 10, n. 13, p. 2230, doi. 10.1002/cbic.200900102
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- Article
Vanadium Chloroperoxidase as a Catalyst for Hydrogen Peroxide Disproportionation to Singlet Oxygen in Mildly Acidic Aqueous Environment.
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- Advanced Synthesis & Catalysis, 2003, v. 345, n. 6/7, p. 849, doi. 10.1002/adsc.200303008
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Novel Reductive Amination of Nitriles: An Efficient Route to 5-Hydroxypiperidone-Derived N,N-Acetals.
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- Advanced Synthesis & Catalysis, 2003, v. 345, n. 4, p. 483, doi. 10.1002/adsc.200390054
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Ring-Closing Metathesis of Allylic O, O- and N, O-Acetals.
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- Advanced Synthesis & Catalysis, 2002, v. 344, n. 6/7, p. 736, doi. 10.1002/1615-4169(200208)344:6/7<736::AID-ADSC736>3.0.CO;2-8
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Palladium-Catalyzed Cyclization Reactions of Acetylene-Containing Amino Acids.
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- Advanced Synthesis & Catalysis, 2002, v. 344, n. 1, p. 70, doi. 10.1002/1615-4169(200201)344:1<70::AID-ADSC70>3.0.CO;2-1
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Industrial Biotransformations.
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- Advanced Synthesis & Catalysis, 2001, v. 343, n. 6/7, p. 751, doi. 10.1002/1615-4169(200108)343:6/7<751::AID-ADSC751>3.0.CO;2-M
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A Biocatalytic Route to Enantiomerically Pure Unsaturated α-H-α-Amino Acids.
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- Advanced Synthesis & Catalysis, 2001, v. 343, n. 6/7, p. 662, doi. 10.1002/1615-4169(200108)343:6/7<662::AID-ADSC662>3.0.CO;2-I
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