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2. G. Bassolino, P. Rivera-Fuentes, Chimia, 2016, 70, 796–780. Intracellular Photoactivation and Quantification Using Fluorescence Microscopy: Chemical Tools and Imaging Approaches. Invited review to the special issue "New Faculty in Switzerland"

Tirla, Alina

From Pablo's postdoc, PhD and undergraduate research:

21. Y. Xiong, P. Rivera-Fuentes, E. Sezgin, A. Vargas Jentzsch, C. Eggeling, H. L. Anderson, Org. Lett. 2016, 8, 3666–3669. Photoswitchable Spiropyran Dyads for Biological Imaging.

20. P. Rivera-Fuentes, S. J. Lippard, Acc. Chem. Res. 2015, 48, 2927–2934. Metal-Based Optical Probes for Live Cell Imaging of Nitroxyl (HNO).

19. C. Mügge, T. Marzo, L. Massai, J. Hildebrandt, G. Ferraro, P. Rivera-Fuentes, N. Metzler-Nolte, A. Merlino, L. Messori, W. Weigand, Inorg. Chem. 2015, 54, 8560–8570. Platinum(II) Complexes with O,S Bidentate Ligands: Biophysical Characterization, Antiproliferative Activity, and Crystallographic Evidence of Protein Binding.

18. P. Rivera-Fuentes, A. T. Wrobel, M. L. Zastrow, M. Khan, J. Georgiou, T. Luyben, J. C. Roder, K. Okamoto, S. J. Lippard, Chem. Sci. 2015, 6, 1944–1948. A Far-Red Emitting Probe for Unambiguous Detection of Mobile Zinc in Acidic Vesicles and Deep Tissue.

17. P. Rivera-Fuentes, S. J. Lippard, ChemMedChem, 2014, 9, 1238–1243. SpiroZin1: A Reversible and pH-Insensitive, Reaction-based, Red-fluorescent Probe for Imaging Biological Mobile Zinc.

16. A. T. Wrobel, T. C. Johnstone, A. D. Liang, S. J. Lippard, P. Rivera-Fuentes, J. Am. Chem. Soc. 2014, 136, 4697–4705. A Fast and Selective Near-Infrared Fluorescent Sensor for Multicolor Imaging of Biological Nitroxyl (HNO).

15. P. Rivera-Fuentes, M. von Wantoch Rekowski, W. B. Schweizer, J.-P. Gisselbrecht, C. Boudon, F. Diederich, Org. Lett. 2012, 14, 4066–4069. Cascade Carbopalladation Reaction between Alkynes and gem-Dibromoolefins: Facile Access to Monoannelated Pentalenes.

14. V. Ehmke, J. E. Q. Quinsaat, P. Rivera-Fuentes, C. Heindl, C. Freymond, M. Rottmann, R. Brun, T. Schirmeister, F. Diederich, Org. Biomol. Chem. 2012, 10, 5764–5768. Tuning and Predicting Biological Affinity: Aryl Nitriles as Cysteine Protease Inhibitors.

13. P. Rivera-Fuentes, F. Diederich, Angew. Chem. Int. Ed. 2012, 51, 2818–2828. Allenes in Molecular Materials.

12. C. M. Reisinger, P. Rivera-Fuentes, S. Lampart, W. B. Schweizer, F. Diederich, Chem. Eur. J. 2011, 17, 12906–12911. Cascade Pericyclic Reactions of Alleno-Acetylenes: Facile Access to Highly Substituted Cyclobutene, Dendralene, Pentalene, and Indene Skeletons.

11. F. Silvestri, M. Jordan, K. Howes, M. Kivala, P. Rivera-Fuentes, C. Boudon, J.-P. Gisselbrecht, W. B. Schweizer, P. Seiler, M. Chiu, F. Diederich, Chem. Eur. J. 2011, 17, 6088–6097. Regular Acyclic and Macrocyclic [AB] Oligomers by Formation of Push-Pull Chromophores in the Chain-Growth Step.

10. P. Rivera-Fuentes, B. Nieto-Ortega, W. B. Schweizer, J. T. López Navarrete, J. Casado, F. Diederich, Chem. Eur. J. 2011, 17, 3876–3885. Enantiopure, Monodisperse Alleno-acetylenic Cyclooligomers: Effect of Symmetry and Conformational Flexibility on the Chiroptical Properties of Carbon-rich Compounds.

9. P. Rivera-Fuentes, J. L. Alonso-Gómez, A. G. Petrovic, F. Santoro, P. Seiler, N. Harada, N. Berova, H. S. Rzepa, F. Diederich, Chem. Eur. J. 2010, 16, 9796–9807. Enantiomerically Pure Alleno-acetylenic Macrocycles: Synthesis, Solid State Structures, Chiroptical Properties, and Electron Localization Function Analysis.

8. A. Kraszewska, P. Rivera-Fuentes, G. Rapenne, J. Crassous, A. G. Petrovic, J. L. Alonso-Gómez, E. Huerta, F. Diederich, C. Thilgen, Eur. J. Org. Chem. 2010, 4402–4411. Regioselectivity in Tether Directed Remote Functionalization - Reinvestigation of the Addition of a CTV Based Tris-Tether to C60.

7. B. Buschhaus, V. Convertino, P. Rivera-Fuentes, J. L. Alonso-Gómez, A. G. Petrovic, F. Diederich, Eur. J. Org. Chem. 2010, 2452–2456. Optically Active Trialkynyl(phenyl)methane: Synthesis and Determination of its Absolute Configuration by Vibrational Circular Dichroism (VCD) and Optical Rotatory Dispersion (ORD).

6. M. Yamada, P. Rivera-Fuentes, W. B. Schweizer, F. Diederich, Angew. Chem. Int. Ed. 2010, 49, 3532–3535. Optical Stability of Axially Chiral Push-Pull-Substituted Buta-1,3-dienes: Effect of a Single Methyl Group on the C60 Surface.

5. P. Rivera-Fuentes, J. L. Alonso-Gómez, A. G. Petrovic, F. Santoro, N. Harada, N. Berova, F. Diederich, Angew. Chem. Int. Ed. 2010, 49, 2247–2250. Amplification of Chirality in Monodisperse, Enantiopure Alleno-acetylenic Oligomers.

4. J. L. Alonso-Gómez, P. Rivera-Fuentes, N. Harada, N. Berova, F. Diederich, Angew. Chem. Int. Ed. 2009, 38, 5545–5548. An Enantiomerically Pure Alleno-acetylenic Macrocycle: Synthesis and Rationalization of its Outstanding Chiroptical Response.

3. J. L. Alonso-Gómez, A. G. Petrovic, N. Harada, P. Rivera-Fuentes, N. Berova, F. Diederich, Chem. Eur. J. 2009, 15, 8396–8400. Chiral Induction from Allenes to Twisted Tetracyanobutadienes (TCBDs): Conformational Assignment by Circular Dichroism (CD) Spectroscopy.

2. A. Kraszewska, P. Rivera-Fuentes, C. Thilgen, F. Diederich, New J. Chem. 2009, 33, 386–396. First Enantiomerically Pure C70-Adducts with a Non-inherently Chiral Addition Pattern.

1. J. L. Alonso-Gómez, P. Schanen, P. Rivera-Fuentes, P. Seiler, F. Diederich, Chem. Eur. J. 2008, 14, 10564–10568. 1,3-Diethynylallenes (DEAs): Enantioselective Synthesis, Absolute Configuration, and Chiral Induction in 1,1,4,4-Tetracyanobuta-1,3-dienes (TCBDs).


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