Publikationen mit Produkten von Varimol
9. Lorenzo Bonaldi, Marco Bortoluzzi, Stefano Zacchini, Guido Pampaloni, Fabio Marchetti*, and Lorenzo Biancalana*; Inorg. Chem. 2023, 62, 20, 7814.
Triazine Chalcogenes from Thiocyanate or Selenocyanate Addition to Tetrazine Ligands in Ruthenium Arene Complexes, DOI.
8. Marc Schnierle, Sina Klostermann, Elif Kaya, Zheng Li, Daniel Dittmann, Carolin Rieg, Deven P. Estes*, Johannes Kästner, Mark R. Ringenberg, and Michael Dyballa*; Inorg Chem. 2023, 62, 19, 7283.
How Solid Surfaces Control Stability and Interactions of Supported Cationic Cu(dppf) Complexes – A Solid-State NMR Study, DOI.
7. Helen Damerow, Xia Cheng, Valeska von Kiedrowski, Ralf Schirrmacher, Björn Wängler, Gert Fricker, Carmen Wängler*; Pharmaceutics 2022, 14, 2114.
Toward Optimized 89Zr‐Immuno‐PET: Side‐by‐Side Comparison of [89Zr]Zr‐DFO‐, [89Zr]Zr‐3,4,3‐(LI‐1,2‐HOPO)‐ and [89Zr]Zr‐DFO*‐Cetuximab for Tumor Imaging: Which Chelator Is the Most Suitable? DOI.
6. Wolfgang Kaim*, Isabell Löw, Mark R. Ringenberg, Brigitte Schwederski, Vasileios Filippou, Jan Fiedler; Z. Anorg. Allg. Chem. 2022.
Tetrazine Chelate Ligands Bridging Two [Ru(acac)2] Fragments: Mixed Valency and Radical Complex Formation, DOI.
5. Marc Schnierle, Mario Winkler, Vasileios Filippou, Joris van Slageren*, Mark R. Ringenberg*; Eur. J. Inorg. Chem. 2022.
(Spectro)Electrochemistry of 3-(Pyrid-2-yl)-s-Tetrazine- and 1,2-(Dihydro)pyridazine Tricarbonylrhenium(I)chloride, DOI.
4. Helen Damerow, Ralph Hübner, Benedikt Judmann, Ralf Schirrmacher, Björn Wängler, Gert Fricker, Carmen Wängler*; Cancers 2021, 13, 6349.
Side-by-Side Comparison of Five Chelators for 89Zr-Labeling of Biomolecules: Investigation of Chemical/Radiochemical Properties and Complex Stability, DOI.
3. Aneta Turlik, K. N. Houk, Dennis Svatunek*; J. Org. Chem. 2021, 86, 13129-13133.
Origin of Increased Reactivity in Rhenium-Mediated Cycloadditions of Tetrazines, DOI.
2. Marc Schnierle, Marie Leimkühler, Mark R. Ringenberg*; Inrog. Chem. 2021, 60, 6367-6374
[(η6 -p-Cymene)[3-(pyrid-2-yl)-1,2,4,5-tetrazine]chlororuthenium(II)]+ , Redox Noninnocence and Dienophile Addition to Coordinated Tetrazine, DOI.
1. Marc Schnierle, Svenja Blickle, Vasileios Filippou*, Mark R. Ringenberg*; Chem. Commun. 2020, 56, 12033-12036.
Tetrazine metallation boosts rate and regioselectivity of inverse electron demand Diels–Alder (iEDDA) addition of dienophiles, DOI.