
6th Swiss Industrial Chemistry Symposium
30. January 2026, Biozentrum Basel

6th Swiss Industrial Chemistry Symposium 2026
30. January 2026,Biozentrum Basel

6th Swiss Industrial Chemistry Symposium
30. January 2026, Biozentrum Basel

6th Swiss Industrial Chemistry Symposium 2026
30. January 2026,Biozentrum Basel
The poster session takes place during the lunch time, from 12.00h - 14.00h.
Make sure that you pin you poster to the panel until the end of the morning coffee break.
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[01] Uwe Albrecht, Corden Pharma Switzerland LLC
Lipids for conjugation – The key to targeted LNPs
[02] Arian Bajramaj, HEIA Fribourg
An Industrial Approach for the Synthesis of functionalized-Xylose via Transacetalization
[03] Wiktor Bohusz, Adam Mickiewicz University in Poznan
Cyclo(alkyl)(amino)carbenes (CAAC): synthesis of ligand salts and their selected metal complexes
[04] Corentin Bon, University of Basel
General Platform for Divergent Construction of Phosphorus-Modified DNA/RNA Backbones
[05] Anton Budeev, University of Basel
Synthesis of phosphorothioates by sulfur transfer from thiosulfate
[06] Lucas Carreras Vinent, Johnson Matthey
Life-cycle assessment of ruthenium catalysts for asymmetric transfer hydrogenation
[07] Paula Chirila, Johnson Matthey
Introduction to DyadPalladate™ Precatalysts and Insights Into Their Activation Mechanism
[08] Adriana Faraone, EPFL Lausanne
Asymmetric Ring-Expansion of Activated Cyclopropanes via Peptide and Photoredox Catalysis
[09] Cristina Lia Fernandez Regueiro, inseit
From Surface Analysis to Process Intensification: Data Driven Immobilization Workflow of Ene-Reductases
[10] Arianna Fuggetti, University of Geneva
Identification of Twenty Proteinogenic Amino Acids using an Engineered Aerolysin Nanopore
[11] Souvik Guha, HEIA Fribourg
Mechanochemically Accelerated N-Arylation: A Scalable and Solvent-Minimized Approach Bypassing Friction Sensitive Reagents
[12] Kamil Hanek, Adam Mickiewicz University in Poznan
Bulky carbenes in chemoselective synthesis of bis(thioesters) from acroleins
[13] Ida Hipfinger, ETH Zürich
An enzymatic approach to fluorinated pharmaceuticals
[14] Michele Jermini, Exeris SA
Programmatic Ensemble Modeling for Molecular Cost Prediction
[15] Christina Jordan, ETH Zurich
Magnetic Resonance Assays for the Identification of Novel Lectin Inhibitors to Combat Antimicrobial Resistance
[16] Katarina Korlova, Novartis Pharma AG
An LC-based Determination of Palladium Residues after Digestion of Complex Organic Matrices
[17] Matthias Lehmann, Syngenta Crop Protection AG
Introducing HEIDI: High Throughput ElectrosynthesIs DevIce for rapid electrosynthetic methodology development and libraries
[18] Xiao-Yu Li, University of Basel
Stereoselective total synthesis of skew-tetramantane, diamond's chiral core
[19] Haris Majstorovic, University of Basel
Total synthesis of a plant-derived glycoside that attenuates virulence in Pseudomonas aeruginosa
[20] Christine Marty, EPFL Lausanne
Ligand-Directed Site-Selective Cysteine Bioconjugation of the KELCH Domain of KEAP1 with Hypervalent Iodine Reagents
[21] Aleksandra Mermela, Adam Mickiewicz University in Poznań
Advanced sustainable industrial catalysis: manganese complexes with bulky DAB ligands for ketone hydroboration
[22] Marzio Monagheddu, VITO Flemish Institute Technology
A simple and sustainable membrane assisted process for the preparation of macrocyclic musks by ring closing metathesis
[23] Murad Najafov, University of Fribourg
Dynamic Confinement Approach for High Metal Loading Crystalline Single-Atom Catalysts
[24] Nils Ostermann, University of Geneva
Bioelectrocatalysis for Sustainable H2 Production by Hydrogenase Enzymes
[25] Guido Panzarasa, NeoChemurgy GmbH
From waste to value: extraction of phytin from oilseed presscake
[26] Ann-Sophie Paschke, ETH Zurich
Advancing Molecular Editing Through Nitrogen Atom Edits: From Fundamental Reactivity to Late-Stage Functionalization
[27] Esaïe Reusser, HEIA Fribourg
Water-based amide coupling with sustainable xylose acetals as co-solvents: A novel organic base-free strategy
[28] Philippe Roth, WAB Group
Evaluation of scalability parameters in synthesis using agitator bead mills for mechano-chemistry
[29] Víctor Sabanza-Gil, EPFL Lausanne
Generative molecular design with steerable and granular synthesizability control
[30] Stefanie Schiele, ETH Zurich
Chemodivergent C-to-N atom swap from benzofurans to benzisoxazoles and benzoxazoles
[31] Evelyn Sgroi, University of Bern
Mining for Novel Tryptophanase A: extremophilic organisms Ardenticatena maritima and Haloarcula japonica as alternative to E. Coli in the synthesis of tryptophan analogues
[32] Sheetal Sheetal, University of Geneva
Atropisomerism and Conformational Dynamics in Dioxa[6]helicene Enamine Constructs with Near-Infrared Absorption and Emission
[33] Joana Silva, CordenPharma Switzerland LLC
Multicomponent Design to Unlock New Opportunities for Topical Drugs
[34] Thordis Snaedal, University of Bern
Two-step Whole-cell Biocatalytic Cascade with in-situ Smart Amine Donor Synthesis
[35] Chloé Stoll, University of Geneva
Chiral Imidazo[1,5-α]pyridine-Based Ligands for the Au-Catalyzed Enantioselective Intramolecular Hydrocarboxylation of Allenes
[36] Harald Todt, Magritek GmbH
Integration Benchtop NMR into synthesis: A path from Manual Sampling over following the reaction in the two different phases simultaneously on-line towards AI-Enabled Self-Optimization of a reaction
[37] Coralie Tournier, University of Geneva
Nanopore-based Identification of Histone 3 Post-Translational Modifications
[38] Fabio Visentin, Mettler Toledo
Scale-up of Hydrogenation of Nitrobenzene, Data-Rich Experimentation approach
[39] Mingming Wang, Max-Planck Institute for Medicinal Research
Late-stage introduction of sulfonamide into electron-rich aromatics
[40] Sylvie Wigmans, HEIA Fribourg & EPFL Lausanne
Pilot Scale-up Strategies for Biobased Acetal Monomers in High-performance Polymers
[41] Jason Williams, Jiuzhou Pharma Europe GmbH
From Lab Keys to Tech Transfer in 12 Months: A Story of Rapidly-Established Modern CRO Labs
[42] Cédric Fries, SpiroChem AG
Early PR&D at SpiroChem: CEP-439, from the MedChem route to the first scale-up