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Asymmetrische reduktive Carbocyclisierung durch modifizierte En‐Reduktasen.
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- Angewandte Chemie, 2018, v. 130, n. 24, p. 7360, doi. 10.1002/ange.201802962
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- Article
Biosynthese des enterotoxischen Pyrrolobenzodiazepin-Naturstoffs Tilivallin.
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- Angewandte Chemie, 2017, v. 129, n. 46, p. 14948, doi. 10.1002/ange.201707737
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- Article
Asymmetric Reductive Carbocyclization Using Engineered Ene Reductases.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 24, p. 7240, doi. 10.1002/anie.201802962
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Biosynthesis of the Enterotoxic Pyrrolobenzodiazepine Natural Product Tilivalline.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 46, p. 14753, doi. 10.1002/anie.201707737
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- Article
Application of Threonine Aldolases for the Asymmetric Synthesis of α‐Quaternary α‐Amino Acids.
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- ChemCatChem, 2018, v. 10, n. 16, p. 3453, doi. 10.1002/cctc.201800611
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- Article
Aktivitätsbasierte Sondenmoleküle zur Untersuchung der Aktivität Flavin-abhängiger Oxidasen und zum Zielprotein-Profiling von Monoaminooxidase-Inhibitoren.
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- Angewandte Chemie, 2012, v. 124, n. 28, p. 7142, doi. 10.1002/ange.201201955
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Discovery, characterization, and comparative analysis of new UGT72 and UGT84 family glycosyltransferases.
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- Communications Chemistry, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42004-024-01231-1
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A Modular Synthesis of Teraryl‐Based α‐Helix Mimetics, Part 5: A Complete Set of Pyridine Boronic Acid Pinacol Esters Featuring Side Chains of Proteinogenic Amino Acids.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 17, p. 1, doi. 10.1002/ejoc.202101280
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- Article
A Modular Synthesis of Teraryl‐Based α‐Helix Mimetics, Part 4: Core Fragments with Two Halide Leaving Groups Featuring Side Chains of Proteinogenic Amino Acids.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 17, p. 1, doi. 10.1002/ejoc.202101279
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- Article
A Modular Synthesis of Teraryl‐Based α‐Helix Mimetics, Part 3: Iodophenyltriflate Core Fragments Featuring Side Chains of Proteinogenic Amino Acids.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 17, p. 1, doi. 10.1002/ejoc.202101278
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- Article
Reaction intensification for biocatalytic production of polyphenolic natural product di‐C‐β‐glucosides.
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- Biotechnology & Bioengineering, 2023, v. 120, n. 6, p. 1506, doi. 10.1002/bit.28354
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Synthesis of a Bcl9 Alpha-Helix Mimetic for Inhibition of PPIs by a Combination of Electrooxidative Phenol Coupling and Pd-Catalyzed Cross Coupling †.
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- Catalysts (2073-4344), 2020, v. 10, n. 3, p. 340, doi. 10.3390/catal10030340
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- Article
Structural Changes in the Cap of Rv0183/mtbMGL Modulate the Shape of the Binding Pocket.
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- Biomolecules (2218-273X), 2021, v. 11, n. 9, p. 1299, doi. 10.3390/biom11091299
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A New Strategy in Heterogeneous Catalysis: The Design of Cortex Catalysts.
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- Angewandte Chemie International Edition, 1996, v. 34, n. 23/24, p. 2728, doi. 10.1002/anie.199527281
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- Article
Loop 6 and the β‐hairpin flap are structural hotspots that determine cofactor specificity in the FMN‐dependent family of ene‐reductases.
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- FEBS Journal, 2024, v. 291, n. 7, p. 1560, doi. 10.1111/febs.17055
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Front Cover: Constraining and Modifying Peptides Using Pd‐Mediated Cysteine Allylation (ChemBioChem 13/2023).
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- ChemBioChem, 2023, v. 24, n. 13, p. 1, doi. 10.1002/cbic.202300340
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Constraining and Modifying Peptides Using Pd‐Mediated Cysteine Allylation.
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- ChemBioChem, 2023, v. 24, n. 13, p. 1, doi. 10.1002/cbic.202300098
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Activity‐Based Protein Profiling (ABPP) of Oxidoreductases.
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- ChemBioChem, 2021, v. 22, n. 4, p. 630, doi. 10.1002/cbic.202000542
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Tracking Protein S-Fatty Acylation with Proteomics.
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- ChemBioChem, 2016, v. 17, n. 16, p. 1488, doi. 10.1002/cbic.201600314
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Chemical Genetic Approaches for the Investigation of Neutral Lipid Metabolism.
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- ChemBioChem, 2016, v. 17, n. 5, p. 358, doi. 10.1002/cbic.201500501
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More than just a Halogenase: Modification of Fatty Acyl Moieties by a Trifunctional Metal Enzyme.
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- ChemBioChem, 2014, v. 15, n. 4, p. 567, doi. 10.1002/cbic.201300345
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Trendbericht Organische Chemie 2024.
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- Nachrichten aus der Chemie, 2024, v. 72, n. 3, p. 44, doi. 10.1002/nadc.20244139258
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Trendbericht Organische Chemie 2023.
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- Nachrichten aus der Chemie, 2023, v. 71, n. 3, p. 40, doi. 10.1002/nadc.20234135542
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Trendbericht Organische Chemie 2022.
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- Nachrichten aus der Chemie, 2022, v. 70, n. 3, p. 42, doi. 10.1002/nadc.20224122453
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Organische Chemie.
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- Nachrichten aus der Chemie, 2021, v. 69, n. 3, p. 38, doi. 10.1002/nadc.20214105947
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Organische Chemie.
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- Nachrichten aus der Chemie, 2020, v. 68, n. 3, p. 42, doi. 10.1002/nadc.20204095515
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- Article
Organische Chemie.
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- Nachrichten aus der Chemie, 2019, v. 67, n. 3, p. 46, doi. 10.1002/nadc.20194085243
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- Article
Trendbericht Organische Chemie 2017.
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- Nachrichten aus der Chemie, 2018, v. 66, n. 3, p. 249, doi. 10.1002/nadc.20184072148
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Organische Chemie 2016.
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- Nachrichten aus der Chemie, 2017, v. 65, n. 3, p. 266, doi. 10.1002/nadc.20174059831
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Organische Chemie.
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- Nachrichten aus der Chemie, 2016, v. 64, n. 3, p. 255, doi. 10.1002/nadc.20164047492
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Festphasen- und Flowsynthese.
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- Nachrichten aus der Chemie, 2015, v. 63, n. 3, p. 273
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Biosynthese der Phenazine.
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- Nachrichten aus der Chemie, 2014, v. 62, n. 10, p. 975, doi. 10.1002/nadc.201490357
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- Article
Pharmacological inhibition of adipose tissue adipose triglyceride lipase by Atglistatin prevents catecholamine-induced myocardial damage.
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- Cardiovascular Research, 2022, v. 118, n. 11, p. 2488, doi. 10.1093/cvr/cvab182
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- Article
Selective Formation of 4,4′‐Biphenols by Anodic Dehydrogenative Cross‐ and Homo‐Coupling Reaction.
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- Chemistry - A European Journal, 2019, v. 25, n. 11, p. 2713, doi. 10.1002/chem.201805737
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Corrigendum: Pharmacological inhibition of adipose triglyceride lipase corrects high-fat diet-induced insulin resistance and hepatosteatosis in mice.
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- Nature Communications, 2017, v. 8, n. 4, p. 15490, doi. 10.1038/ncomms15490
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Pharmacological inhibition of adipose triglyceride lipase corrects high-fat diet-induced insulin resistance and hepatosteatosis in mice.
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- Nature Communications, 2017, v. 8, n. 3, p. 14859, doi. 10.1038/ncomms14859
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Size-Selective Electrochemical Preparation of Surfactant-Stabilized Pd-, Ni- and Pt/Pd Colloids.
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- Chemistry - A European Journal, 2001, v. 7, n. 5, p. 1084, doi. 10.1002/1521-3765(20010302)7:5<1084::AID-CHEM1084>3.0.CO;2-J
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Site-Selective Protein Immobilization by Staudinger LigationThis research was supported by the Volkswagen Stiftung, the Max Planck Gesellschaft, and the Fonds der Chemischen Industrie.
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- Angewandte Chemie, 2006, v. 118, n. 9, p. 1436, doi. 10.1002/ange.200502057
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- Article
Evaluation of Enzyme Inhibitors in Drug Discovery. Von Robert A. Copeland.
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- Angewandte Chemie, 2005, v. 117, n. 40, p. 6603, doi. 10.1002/ange.200585328
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- Article
Molecular Biology in Medicinal Chemistry. Band 21 der Reihe Methods and Principles in Medicinal Chemistry. Herausgegeben von Theodor Dingermann, Dieter Steinhilber und Gerd Folkers.
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- Angewandte Chemie, 2004, v. 116, n. 27, p. 3592, doi. 10.1002/ange.200385131
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- Article
Die Staudinger-Ligation – ein Geschenk für die Chemische Biologie.
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- Angewandte Chemie, 2004, v. 116, n. 24, p. 3168, doi. 10.1002/ange.200401744
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- Article
Der Gipfel der Stereochemie: Bürgenstock 2004.
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- Angewandte Chemie, 2004, v. 116, n. 23, p. 3048, doi. 10.1002/ange.200460496
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Elektroorganische Synthese an der festen Phase mit Polymerkügelchen als Trägermaterial ( Diese Arbeit wurde von der Max-Planck-Gesellschaft (Doktorandenstipendium für S.N.), dem Fonds der Chemischen Industrie (Liebig-Stipendium für R.B.), der Deutschen Forschungsgemeinschaft (Br2324/1-1) und dem Land Nordrhein-Westfalen gefördert. R.B. dankt Prof. H. Waldmann für seine fortlaufende Unterstützung. )
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- Angewandte Chemie, 2004, v. 116, n. 17, p. 2347, doi. 10.1002/ange.200352674
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Staudinger-Ligation: eine Immobilisierungsstrategie zur Herstellung von Wirkstoff-Arrays ( Diese Arbeit wurde von der Deutschen Forschungsgemeinschaft, der Max-Planck-Gesellschaft, der Alexander von Humboldt-Stiftung (Forschungsstipendium für L.S.) und dem Fonds der Chemischen Industrie (Liebig-Stipendium für R.B.) finanziell unterstützt. Wir danken der Universität Dortmund für finanzielle Förderung im Rahmen des Forschungsprogramms Molekulare Grundlagen der Biowissenschaften. )
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- Angewandte Chemie, 2003, v. 115, n. 47, p. 6010, doi. 10.1002/ange.200352877
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- Article
Stereochemistry and Mechanism of Enzymatic and Non-Enzymatic Hydrolysis of Benzylic sec-Sulfate Esters.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 18, p. 3930, doi. 10.1002/ejoc.201402211
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Solid-supported reagents and catalysts for the preparation of large ring compounds.
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- Molecular Diversity, 2005, v. 9, n. 1-3, p. 51, doi. 10.1007/s11030-005-1308-8
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- Article
Site-Selective Protein Immobilization by Staudinger LigationThis research was supported by the Volkswagen Stiftung, the Max Planck Gesellschaft, and the Fonds der Chemischen Industrie.
- Published in:
- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1408, doi. 10.1002/anie.200502057
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- Article
Evaluation of Enzyme Inhibitors in Drug Discovery. By Robert A. Copeland.
- Published in:
- Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6445, doi. 10.1002/anie.200585328
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- Publication type:
- Article
Molecular Biology in Medicinal Chemistry. (Series: Methods and Principles in Medicinal Chemistry, Vol. 21.) Edited by Theodor Dingermann, Dieter Steinhilber and Gerd Folkers.
- Published in:
- Angewandte Chemie International Edition, 2004, v. 43, n. 27, p. 3510, doi. 10.1002/anie.200385131
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- Article
The Staudinger Ligation—A Gift to Chemical Biology.
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- Angewandte Chemie International Edition, 2004, v. 43, n. 24, p. 3106, doi. 10.1002/anie.200401744
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- Article