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Front Cover: Crystallization Assisted Dynamic Kinetic Resolution for the Synthesis of (R)‐β‐Methylphenethylamine (ChemBioChem 16/2024).
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- ChemBioChem, 2024, v. 25, n. 16, p. 1, doi. 10.1002/cbic.202481601
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Crystallization Assisted Dynamic Kinetic Resolution for the Synthesis of (R)‐β‐Methylphenethylamine.
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- ChemBioChem, 2024, v. 25, n. 16, p. 1, doi. 10.1002/cbic.202400203
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- Article
Rationalizing the Unprecedented Stereochemistry of an Enzymatic Nitrile Synthesis through a Combined Computational and Experimental Approach.
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- Angewandte Chemie, 2021, v. 133, n. 35, p. 19311, doi. 10.1002/ange.202017234
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- Article
Segmentierte Flow‐Prozesse zur Überwindung von Limitierungen der Ganzzell‐Biokatalyse in Gegenwart von organischen Lösungsmitteln.
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- Angewandte Chemie, 2021, v. 133, n. 29, p. 15997, doi. 10.1002/ange.202015887
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- Article
Effect of Particle Wettability and Particle Concentration on the Enzymatic Dehydration of n‐Octanaloxime in Pickering Emulsions.
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- Angewandte Chemie, 2021, v. 133, n. 3, p. 1470, doi. 10.1002/ange.202013171
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Rücktitelbild: Cyanid-freie und breit anwendbare enantioselektive Syntheseplattform für chirale Nitrile durch einen biokatalytischen Zugang (Angew. Chem. 40/2017).
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- Angewandte Chemie, 2017, v. 129, n. 40, p. 12546, doi. 10.1002/ange.201707179
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- Article
Cyanid-freie und breit anwendbare enantioselektive Syntheseplattform für chirale Nitrile durch einen biokatalytischen Zugang.
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- Angewandte Chemie, 2017, v. 129, n. 40, p. 12533, doi. 10.1002/ange.201702952
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- Article
Ein-Topf-Reaktionskaskaden durch Kombination einer eingekapselten Decarboxylase mit Metathese zur Synthese biobasierter Antioxidantien.
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- Angewandte Chemie, 2016, v. 128, n. 47, p. 15043, doi. 10.1002/ange.201607777
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The function of the oxylipin 12-oxophytodienoic acid in cell signaling, stress acclimation, and development.
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- Journal of Experimental Botany, 2018, v. 69, n. 22, p. 5341, doi. 10.1093/jxb/ery316
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- Article
Front Cover: Kinetic Resolution of Cyclic Tertiary Alcohols with Lipase A from Candida Antarctica (Eur. J. Org. Chem. 21/2024).
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- European Journal of Organic Chemistry, 2024, v. 27, n. 21, p. 1, doi. 10.1002/ejoc.202482101
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Kinetic Resolution of Cyclic Tertiary Alcohols with Lipase A from Candida Antarctica.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 21, p. 1, doi. 10.1002/ejoc.202400242
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- Article
Cyanide-Free and Broadly Applicable Enantioselective Synthetic Platform for Chiral Nitriles through a Biocatalytic Approach.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 40, p. 12361, doi. 10.1002/anie.201702952
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Back Cover: Cyanide-Free and Broadly Applicable Enantioselective Synthetic Platform for Chiral Nitriles through a Biocatalytic Approach (Angew. Chem. Int. Ed. 40/2017).
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- Angewandte Chemie International Edition, 2017, v. 56, n. 40, p. 12374, doi. 10.1002/anie.201707179
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- Article
A One-Pot Cascade Reaction Combining an Encapsulated Decarboxylase with a Metathesis Catalyst for the Synthesis of Bio-Based Antioxidants.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 47, p. 14823, doi. 10.1002/anie.201607777
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Enantiomerically Pure Tribenzotriquinacenes through Stereoselective Synthesis.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 46, p. 13764, doi. 10.1002/anie.201506906
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Cooperative Catalysis of Noncompatible Catalysts through Compartmentalization: Wacker Oxidation and Enzymatic Reduction in a One-Pot Process in Aqueous Media.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 15, p. 4488, doi. 10.1002/anie.201409590
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An Enzyme Cascade Synthesis of ε-Caprolactone and its Oligomers.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 9, p. 2784, doi. 10.1002/anie.201410633
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- Article
Hydroxy Functionalization of Non-Activated CH and CC Bonds: New Perspectives for the Synthesis of Alcohols through Biocatalytic Processes.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 12, p. 3067, doi. 10.1002/anie.201308556
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Highly Enantioselective Reduction of α-Methylated Nitroalkenes.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 35, p. 9323, doi. 10.1002/anie.201301814
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Flow Biocatalysis: A Challenging Alternative for the Synthesis of APIs and Natural Compounds.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 3, p. 990, doi. 10.3390/ijms22030990
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Designer organisms.
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- Chemistry & Industry, 2005, n. 9, p. 21
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Rational Biocatalyst Design for a Cyanide‐Free Synthesis of Long‐Chain Fatty Nitriles from Their Aldoximes.
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- European Journal of Lipid Science & Technology, 2023, v. 125, n. 5, p. 1, doi. 10.1002/ejlt.202200177
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Selective Hydrogenation of Fatty Nitriles to Primary Fatty Amines: Catalyst Evaluation and Optimization Starting from Octanenitrile.
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- European Journal of Lipid Science & Technology, 2020, v. 122, n. 1, p. N.PAG, doi. 10.1002/ejlt.201900163
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Overcoming Work‐Up Limitations of Biphasic Biocatalytic Reaction Mixtures Through Liquid‐Liquid Segmented Flow Processes.
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- ChemCatChem, 2019, v. 11, n. 23, p. 5788, doi. 10.1002/cctc.201901107
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Catalysts Encapsulated in Biopolymer Hydrogels for Chemoenzymatic One‐Pot Processes in Aqueous Media.
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- ChemCatChem, 2019, v. 11, n. 5, p. 1504, doi. 10.1002/cctc.201802070
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- Article
Novel Insights into the Combination of Metal‐ and Biocatalysis: Cascade One‐Pot Synthesis of Enantiomerically Pure Biaryl Alcohols in Deep Eutectic Solvents.
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- ChemCatChem, 2018, v. 10, n. 19, p. 4417, doi. 10.1002/cctc.201800768
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'Side-Product Catalysis': Substrate Autoxidation as an Overlooked Side Reaction Generating a Co-Catalyst for Enhancing Asymmetric Aldol Reactions.
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- ChemCatChem, 2017, v. 9, n. 8, p. 1383, doi. 10.1002/cctc.201601530
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Formal Enantioselective Hydroamination of Non-Activated Alkenes: Transformation of Styrenes into Enantiomerically Pure 1-Phenylethylamines in Chemoenzymatic One-Pot Synthesis.
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- ChemCatChem, 2017, v. 9, n. 4, p. 555, doi. 10.1002/cctc.201601463
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A Fed-Batch Synthetic Strategy for a Three-Step Enzymatic Synthesis of Poly-ϵ-caprolactone.
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- ChemCatChem, 2016, v. 8, n. 22, p. 3446, doi. 10.1002/cctc.201600806
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Guerbet Alcohols: From Processes under Harsh Conditions to Synthesis at Room Temperature under Ambient Pressure.
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- ChemCatChem, 2016, v. 8, n. 5, p. 895, doi. 10.1002/cctc.201501241
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Biocatalytic Access to Chiral Polyesters by an Artificial Enzyme Cascade Synthesis.
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- ChemCatChem, 2015, v. 7, n. 23, p. 3951, doi. 10.1002/cctc.201500823
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Biocatalytic Reduction of 2‐Monosubstituted 3‐Thiazolines Using Imine Reductases.
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- Journal of Heterocyclic Chemistry, 2019, v. 56, n. 3, p. 788, doi. 10.1002/jhet.3437
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Process Development through Solvent Engineering in the Biocatalytic Synthesis of the Heterocyclic Bulk Chemical e-Caprolactone.
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- Journal of Heterocyclic Chemistry, 2017, v. 54, n. 1, p. 391, doi. 10.1002/jhet.2595
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Enantiomerenreine Tribenzotriquinacene durch stereoselektive Synthese.
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- Angewandte Chemie, 2015, v. 127, n. 46, p. 13968, doi. 10.1002/ange.201506906
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- Article
Kooperative Katalyse nicht-kompatibler Katalysatoren durch Kompartimentierung: Wacker-Oxidation und enzymatische Reduktion in einem Eintopf-Verfahren im wässrigen Medium.
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- Angewandte Chemie, 2015, v. 127, n. 15, p. 4570, doi. 10.1002/ange.201409590
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- Article
Eine Enzymkaskade zur Synthese von ε-Caprolacton und dessen Oligomeren.
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- Angewandte Chemie, 2015, v. 127, n. 9, p. 2825, doi. 10.1002/ange.201410633
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- Article
Hydroxy-Funktionalisierung nichtaktivierter C-H- und CC-Bindungen: Neue Perspektiven für die Synthese von Alkoholen durch biokatalytische Verfahren.
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- Angewandte Chemie, 2014, v. 126, n. 12, p. 3128, doi. 10.1002/ange.201308556
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- Article
Hochenantioselektive Reduktion von α-methylierten Nitroalkenen.
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- Angewandte Chemie, 2013, v. 125, n. 35, p. 9493, doi. 10.1002/ange.201301814
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- Article
Direktoxidation von Cycloalkanen zu Cycloalkanonen mit Sauerstoff in Wasser.
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- Angewandte Chemie, 2013, v. 125, n. 8, p. 2415, doi. 10.1002/ange.201204464
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Gesteuerte kinetisch oder thermodynamisch kontrollierte Organokatalyse und Anwendung in der chemoenzymatischen Synthese.
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- Angewandte Chemie, 2011, v. 123, n. 34, p. 8092, doi. 10.1002/ange.201008042
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Eisenkatalyse zur In-situ-Regenerierung oxidierter Cofaktoren durch Aktivierung und Reduktion von O.
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- Angewandte Chemie, 2011, v. 123, n. 10, p. 2445, doi. 10.1002/ange.201004101
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Asymmetric reduction of activated alkenes using an enoate reductase from Gluconobacter oxydans.
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- Applied Microbiology & Biotechnology, 2011, v. 89, n. 1, p. 79, doi. 10.1007/s00253-010-2793-y
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Threonine aldolases-screening, properties and applications in the synthesis of non-proteinogenic β-hydroxy-α-amino acids.
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- Applied Microbiology & Biotechnology, 2010, v. 88, n. 2, p. 409, doi. 10.1007/s00253-010-2751-8
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Purification, cloning, and overexpression of an alcohol dehydrogenase from Nocardia globerula reducing aliphatic ketones and bulky ketoesters.
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- Applied Microbiology & Biotechnology, 2010, v. 86, n. 6, p. 1813, doi. 10.1007/s00253-009-2385-x
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Biotransformations with Imine Reductases: Design of a Practical Process Avoiding an Extractive Work‐Up by Entrapment of Water and Enzymes in an Immobilized Phase.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 43, p. 1, doi. 10.1002/ejoc.202300158
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Overcoming Thermodynamically Driven Retro‐Diels–Alder Reaction through a Cascade One‐Pot Process Exemplified for a Bio‐Based Platform Chemical.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 21, p. 1, doi. 10.1002/ejoc.202300018
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Combination of Asymmetric Organo‐ and Biocatalysis in Flow Processes and Comparison with their Analogous Batch Syntheses.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 7, p. 1, doi. 10.1002/ejoc.202101035
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Front Cover: Structure‐Performance Guided Design of Sustainable Plasticizers from Biorenewable Feedstocks (Eur. J. Org. Chem. 45/2021).
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 45, p. 6084, doi. 10.1002/ejoc.202101402
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Structure‐Performance Guided Design of Sustainable Plasticizers from Biorenewable Feedstocks.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 45, p. 6086, doi. 10.1002/ejoc.202101014
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Front Cover: Heterogeneous Catalysts "on the Move": Flow Chemistry with Fluid Immobilised (Bio)Catalysts (Eur. J. Org. Chem. 38/2020).
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 38, p. 6026, doi. 10.1002/ejoc.202001281
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- Article