Publications

12. Light- and Heat-Induced Reversal of Circularly Polarized Luminescence in a Single Molecule.

L. Hardoin, E. Sidler, J. de Boer, G. Delhaye, M. Loumaigne, M. Allain, S. Goeb, A. Ryabchun, M. Sallé, D. Jacquemin, B. L. Feringa*, D. Canevet*, Angew. Chem. Int. Ed. 2026, 138, e22699.

11. Indeno[2,1‐c]fluorene Quasi[8]circulenes Through Intramolecular Cyclization.

E. Sidler*,  R. Hein, C. N. Stindt, B. L. Feringa*, Angew. Chem. Int. Ed. 2025, e202510583.

10. Chiral Induction and Memory via Supramolecular Deracemization.

R. Hein‡, E. Sidler‡, Y. Gisbert, B. L. Feringa, Angew. Chem. Int. Ed. 2025, 64, e202510584.

9. A Cycloparaphenylene Acetylene as Potential Precursor for an Armchair Carbon Nanotube.

E. Sidler, R. Röthlisberger, M. Mayor, Chem. Eur. J. 2024,  30, e202403084.

8. Redox-Switchable Aromaticity in a Helically Extended Indeno[2,1-c]fluorene.

E. Sidler‡, R. Hein‡, D. Doellerer, B. L. Feringa, J. Am. Chem. Soc. 2024,  146, 19168—19176.

7. Circularly Polarized Luminescence of Thiophene‐Bridged Macrocyclic pseudo‐meta [2.2]Paracyclophanes.

C. Kress‡, E. Sidler‡, P. Downey, P. Zwick, O. Fuhr, D. Fenske, S. Bernhard, M. Mayor, Chem. Eur. J. 2024,  30, e202303798.

6. Intense Molar Circular Dichroism in Fully Conjugated All‐Carbon Macrocyclic 1,3‐Butadiyne Linked pseudo‐meta [2.2]Paracyclophanes.

E. Sidler, P. Zwick, C. Kress, K. Reznikova, O. Fuhr, D. Fenske, M. Mayor, Chem. Eur. J. 2022, 28, e202201764.

5. Induced axial chirality by a tight belt: naphthalene chromophores fixed in a 2, 5-substituted cofacial para-phenylene–ethynylene framework.

E. Sidler, J. Malinčík, A. Prescimone, M. Mayor, J. Mater. Chem. C 2021, 9, 16199—16207.

4. Toward a Scalable Synthesis and Process for EMA401, Part II: Development and Scale-Up of a Pyridine-and Piperidine-Free Knoevenagel–Doebner Condensation.

E. Sidler, R. Humair, L. A. Hardegger, Org. Process Res. Dev. 2020, 24, 9, 1756—1762.

3. Toward a scalable synthesis and process for EMA401, Part III: using an engineered phenylalanine ammonia lyase enzyme to synthesize a non-natural phenylalanine derivative.

L. A. Hardegger, P. Beney, D. Bixel, C. Fleury, F. Gao, A. Grand-Guillaume Perrenoud, X. Gu, J. Haber, T. Hong, R. Humair, A. Kaegi, M. Kibiger, F. Kleinbeck, V. Tong Luu, L. Padeste, F. A. Rampf, T. Ruch, T. Schlama, E. Sidler, A. Udvarhelyi, B. Wietfeld, Y. Yang, Org. Process Res. Dev. 2020, 24, 9, 1763—1771.

2. Helicene monomers and dimers: chiral chromophores featuring strong circularly polarized luminescence.

C. Schaack‡, L. Arrico‡, E. Sidler, M. Górecki, L. Di Bari, F. Diederich, Chem. Eur. J. 2019, 25, 8003 —8007.

1. Helical threads: enantiomerically pure carbo [6] helicene oligomers.

C. Schaack, E. Sidler, N. Trapp, F. Diederich, Chem. Eur. J. 2017, 23, 14153—14157.