Publications

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

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


Poster

Poster presentation at the "Japanese Society for Chitin and Chitosan"
Poster presentation at the "International Symposium of Green Chemistry 2022"
Poster presentation at the "International Symposium of Green Chemistry 2022"