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Johannes Gutenberg-University Mainz Department of Chemistry Duesbergweg 10–14 Room 1.125 55128 Mainz Phone: +49 6131/39-24381 E-mail: elisabeth.oehl@uni-mainz.de |
| 2015–2019 | Bachelor Studies in Biomedical Chemistry at Mainz University |
| 2017 | Research internship in the Trembleau group and semester abroad at the University of Aberdeen, Scotland |
| 2018 | Bachelor Thesis in the Waldvogel group at Mainz University |
| 2019–2021 | Master Studies in Biomedical Chemistry at Mainz University |
| 2020–2021 | Master Thesis at Sanofi-Aventis Deutschland GmbH |
| 2021-2025 | PhD studies in the Waldvogel Group at Mainz University |
| Research interests: | electroorganic synthesis, renewable resources |
| Publications: |
J. Buchholz, E. K. Oehl, M. M. Hielscher, S. L. Kuhn, D. Schollmeyer, S. R. Waldvogel, Electrochemical Dehydrogenative sp2-Coupling Reaction of Naphthols Accessing a Novel Polycyclic Naphthalenone Motif, Org. Lett. 2024. [DOI: 10.1021/acs.orglett.4c03518]. Elisabeth K. Oehl, Marola S. Lenhard, S. R. Waldvogel, "Tools of Green Synthesis: Electrochemistry" in Encyclopedia of Green Chemistry, 1st Edition, Elsevier, 2024, 10.1016/B978-0-443-15742-4.00108-3. E. K. Oehl, P. T. Jirsch, J. Hammes, A. Stenglein, M. Méndez, S. Ruf, S. R. Waldvogel, Electrochemical Synthesis of a Sitagliptin Precursor, J. Org. Chem. 2024. [DOI: 10.1021/acs.joc.4c00428] B. Pavlovic, C. Heubel, M. Kurz, E. Oehl, S. R. Waldvogel, M. Méndez, S. Ruf, Single Step Synthesis of β- and γ- aryl-substituted β- and γ- Amino Acid Derivatives by Electrochemistry, Bioorg. Med. Chem. Lett., 2024, 100, 129614. [DOI: 10.1016/j.bmcl.2024.129614] M. M. Hielscher, E. K. Oehl, B. Gleede, J. Buchholz, S. R. Waldvogel, Optimization Strategies for the Anodic Phenol-Arene Cross-Coupling Reaction, ChemElectroChem, 2021, 8, 3904–3910. B. Gleede, E. K. Oehl, D. Schollmeyer, S. R. Waldvogel, 4-Hydroxy-3,4',5,5'-tetramethoxy-2'-methylbiphenyl, IUCrData 2019, 4, x191212. |