The Verho Group

The research in Verho’s group spans a wide range of areas, including organic chemistry method development, drug design and development, as well as the creation of new, more efficient electrode materials for green hydrogen production. Currently, this page only describes the latest research on the development of new electrochemical methods for C-H functionalization, but in the future, it will also include descriptions of the group's other research areas.
New Electrochemical C-H Functionalization Methods for a Greener Production of Chemicals
Electrochemistry holds immense potential to enhance the synthesis of a wide range of chemical products. In our research group, we actively work on developing new electrochemical methods that enable C-H functionalization, i.e., the direct transformation of carbon-hydrogen bonds into other more valuable carbon-carbon or carbon-heteroatom bonds, in a more efficient manner. C-H functionalization chemistry is currently one of the most intensely studied research fields in organic chemistry, with numerous applications related to drug development, fine chemical and natural product synthesis, as well as materials science. Our group has previously contributed with several C-H functionalization methods utilizing palladium catalysis in combination with the 8-aminoquinoline directing group to activate C-H bonds in various types of substrate scaffolds.
Unfortunately, these conventional C-H functionalization methods, developed by both us and other research groups, have relied on unsustainable reaction conditions, including high reaction temperatures and large loadings of nobel metal catalysts and silver-based oxidants, which have limited their industrial-scale application. By instead leveraging electrochemistry for C-H functionalization, it becomes possible to conduct these reactions under milder and more environmentally friendly conditions aligned with the principles of green chemistry.
Recently, we have developed more efficient synthetic methods that combine electrochemistry with metal catalysts to achieve C-H functionalization at lower temperatures and without the need for additional redox reagents and additives. Furthermore, we have designed metal-free electrochemical C-H functionalization methods that require only the necessary reagents and working electrodes to function. A common feature of all the methods we develop is that they operate in simple undivided cell setups and are scalable, ensuring their potential for real-world applications. We have already developed several methods that can be used for the synthesis of various useful synthetic building blocks and pharmaceuticals, late-stage functionalization of complex molecules, and biomass valorization.
Selected Publications (C-H functionalization)
An Electrochemical Amidation/C-H Halogenation Cascade for the Sustainable Synthesis of Halogenated N-Aryl Amides, Carbamates and Ureas. S. Ponra, R. Sitdikov, A. Calis, O. Verho*, ChemRxiv 2025, 10.26434/chemrxiv-2025-pjgx8
Cobaltaelectro-Catalyzed C-H Acyloxylation of Aromatic and Vinylic Amide Derivatives at Room Temperature. R. Sitdikov, P. Nikolaienko, L. Meyer, O. Verho*, ChemRxiv 2025, 10.26434/chemrxiv-2025-bbjk3-v2
Regioselective Palladaelectro‐Catalyzed Chlorination of Arenes in an Undivided Cell. S. Ponra, R. Sitdikov, A. Calis, O. Verho*, Adv. Synth. Catal. 2025, 367, e202401298.
Electrochemical Palladium‐Catalyzed Oxidative Carbonylation‐Cyclization of Enallenols. J. Zhang, B. Das, O. Verho, J. -E. Bäckvall, Angew. Chem. Int. Ed. 2022, 134, e202212131
Ru-Catalyzed C-C Bond Formation via C-H Bond Cleavage. Z. Giustra, O. Verho, L. Pilarski, Handbook of CH-Functionalization 2022, https://doi.org/10.1002/9783527834242.chf0034
A Study of an 8-Aminoquinoline-Directed C(sp2)–H Arylation Reaction on the Route to Chiral Cyclobutane Keto Acids from Myrtenal. M. Pourghasmei Lati,* J. Ståhle, M. Oschmann, O. Verho*, J. Org. Chem. 2021, 86, 8527-8537.
Synthesis of Elaborate Benzofuran-2-Carboxamide Derivatives through a Combination of 8-Aminoquinoline Directed C–H Arylation and Transamidation Chemistry. M. Oschmann, L. Johansson Holm, M. Pourghasemi Lati, O. Verho*, Molecules 2020, 25, 361.