26. M. Komabayashi, S. Jopp*, ChemistryEurope 2024, 2, e202400052.

Glucose-based Ionic Liquid Organocatalysts for Asymmetric aza-Diels-Alder Reactions (Open Access)

25. S. Lambrecht, A. Gazizova, S. Kara, J. Meyer*, S. Jopp*, RSC Adv. 2024, 14, 30719–30731.

Antimicrobial properties and biocompatibility of semi-synthetic carbohydrate-based ionic hydrogels (Open Access)

24. S. Lambrecht, M. Biermann, S. Kara, S. Jopp, J. Meyer*, Mater. Adv. 2024, 5, 6957–6966.

A novel characterization technique for hydrogels – in situ rheology-Raman spectroscopy for gelation and polymerization tracking (Open Access)

23. S. Jopp, F. Spruner von Mertz, P. Ehlers, A. Villinger, P. Langer*, Beilstein J. Org. Chem. 2024, 20, 1246–1255.

Synthesis and optical properties of bis- and tris-alkynyl-2-trifluoromethylquinolines (Open Access)

22. H. Ziems, M. Komabayashi, P. Lehmann, A. Villinger, S. Jopp*, Eur. J. Org. Chem. 2024, 27, e202400177.

Structure-Activity Relationships of Glucose-based Pd^II-Bis(NHC) Complexes in a Model Suzuki-Miyaura Reaction (Open Access)

21. S. Lambrecht, H. Schröter, H. Pohle, S. Jopp*, ACS Omega 2024, 9, 5418–5428.

Swelling Behavior of Novel Hydrogels Produced from Glucose-Based Ionic Monomers with Varying Cross-Linkers (Open Access)

20. P. Lehmann, S. Jopp*, Chem. Asian J. 2024, 19, e202300918.

Excellence in acrylation – scope and limitation of glucosyl imidazolium-coated Novozym 435 catalyzed (meth)acryl ester synthesis (Open Access)

19. S. Jopp*, T. Fleischhammer, A. Lavrentieva, S. Kara, J. Meyer*, RSC Sustain. 2023, 1, 1751–1764.

Synthesis, biocompatibility, and antimicrobial properties of glucose-based ionic liquids (Open Access) + Backcover

18. M. Komabayashi, S. Okushiba, T. Nokami, S. Jopp*, Asian J. Org. Chem. 2023, 12, e202300093.

Scope and Limitations in the Synthesis of Glucosamine-based Ionic Liquids (Open Access)

17. P. Lehmann, S. Jopp*, ChemistryOpen 2022, 11, e202200135.

Novel Glucosylimidazolium Ionic-Liquid-Supported Novozym 435 Catalysts – A Proof of Concept for an Acrylation Reaction (Open Access) + Frontcover + Cover Profile

16. S. Lambrecht, A. Villinger, S. Jopp*, IUCrData 2022, 7, x220265.

1-(Methyl-α-D-gluco­pyran­osid-6-yl)-3-vinyl­imidazolium iodide di­methyl­formamide monosolvate (Open Access)

15. J. Schnegas, S. Jopp*, Compounds 2021, 1, 154–163.

Glucosylimidazolium Hydroxide: A Bench-Stable Carbohydrate Based Building Block (Open Access)

14. N. Tka, M. A. H. Ayed, M. B. Braiek, M. Jabli, N. Chaaben, K. Alimi, S. Jopp, P. Langer*, Beilstein J. Org. Chem. 2021,17, 1629–1640.

2,4-Bis(arylethynyl)-9-chloro-5,6,7,8-tetrahydroacridines: synthesis and photophysical properties (Open Access)

13. M. Komabayashi, T. Stiller, S. Jopp*, J. Mol. Liq. 2021, 325, 115167.

Structure-property relationships of ribose based ionic liquids

12. M. Komabayashi, T. Nokami, S. Jopp*, Asian J. Org. Chem. 2020, 9, 2092–2094.

From Chitin to CHILs: First Glucosamine based Ionic Liquids (Open Access) + Frontcover

11. S. Jopp*, Eur. J. Org. Chem. 2020, 6418–6428.

Carbohydrate Based Ionic Liquids (CHILs): Synthesis and Applications (Open Access)

10. M. Reiß, A. Brietzke, T. Eickner, F. Stein, A. Villinger, C. Vogel, U. Kragl, S. Jopp*, RSC Adv. 2020, 10, 14299–14304.

Synthesis of novel carbohydrate based pyridinium ionic liquids and cytotoxicity of ionic liquids for mammalian cells (Open Access)

9. S. Jopp, R. Molenda, E. R. D. Seiler, M. F. Maitz, A. Villinger, P. Ehlers, P. Langer*, ChemistrySelect 2019, 4, 13802–13805.

Total Synthesis of Dabigatran Revisited; Synthesis of Amidine-Tosylated Dabigatran

8. L. Longwitz, S. Jopp, T. Werner*, J. Org. Chem. 2019, 84, 7863−7870.

Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling

7. S. Jopp, P. Ehlers, E. Frank, E. Mernyák, G. Schneider, J. Wölfling, A. Villinger, P. Langer*, Synlett 2019, 30, 600–604.

Site-Selective Synthesis of 3,17-Diaryl-1,3,5,16-estratetraenes

6. S. Jopp, T. Wallaschkowski, P. Ehlers, E. Frank, G. Schneider, J. Wölfling, E. Mernyák, A. Villinger, P. Langer*, Tetrahedron 2018, 74, 2825–2836.

Chemoselective Suzuki-Miyaura reactions of 4-bromo-3-O-triflyl-estrone. Synthesis and atropisomerism of arylated estrones

5. S. Jopp, M. Liesegang, P. Ehlers, E. Frank, G. Schneider, J. Wölfling, P. Langer*, Tetrahedron Lett. 2018, 59, 26–28.

Synthesis of novel 16-E-(arylidene)-3-methoxy-α-estrones via a palladium catalysed Suzuki-Miyaura reaction

4. S. Jopp, M. Liesegang, P. Ehlers, E. Frank, G. Schneider, J. Wölfling, A. Villinger, P. Langer*, Synlett 2017, 28, 2647–2649.

Palladium-Catalysed Sonogashira Reactions of 16-(Hydroxymethylidene)-3-methoxy-α-estrone

3. S. Riebe, S. Jopp, P. Ehlers, E. Frank, G. Schneider, J. Wölfling, A. Villinger, P. Langer*, Tetrahedron Lett. 2017, 58, 2801–2803.

Synthesis of 16-E-([aryl]idene)-3-methoxy-estrones by a palladium catalysed Mizoroki-Heck reaction

2. M.-L. Schirmer, S. Jopp, J. Holz, A. Spannenberg, T. Werner*, Adv. Synth. Catal. 2016, 358, 26–29.

Organocatalyzed Reduction of Tertiary Phosphine Oxides

1. P. Ehlers, A. Petrosyan, J. Baumgard, S. Jopp, N. Steinfeld, T. V. Ghochikyan, A. S. Saghyan, C. Fischer, P. Langer*, ChemCatChem 2013, 5, 2504–2511.

Synthesis of 2,5-Diarylpyrroles by Ligand-Free Palladium-Catalyzed CH Activation of Pyrroles in Ionic Liquids