Professur für Organische Chemie

Adresse:
Nikolaus-Fiebiger-Str. 10
91058 Erlangen


Forschungsprojekt(e)


Waschkraftverstärker 2 - Fortsetzung
Prof. Dr. Jürgen Schatz
(01.10.2012 - 31.10.2013)



Publikationen (Download BibTeX)

Go to first page Go to previous page 1 von 4 Go to next page Go to last page

Heller, B., Kolbeck, C., Niedermaier, I., Dommer, S., Schatz, J., Hunt, P.,... Steinrück, H.-P. (2018). Surface Enrichment in Equimolar Mixtures of Non-Functionalized and Functionalized Imidazolium-Based Ionic Liquids. ChemPhysChem, 19, 1733-1745. https://dx.doi.org/10.1002/cphc.201800216
Heller, B., Kolbeck, C., Niedermaier, I., Dommer, S., Schatz, J., Hunt, P.,... Steinrück, H.-P. (2018). Surface Enrichment in Equimolar Mixtures of Non-Functionalized and Functionalized Imidazolium-Based Ionic Liquids. Chemphyschem, 19(14), 1733-1745. https://dx.doi.org/10.1002/cphc.201800216
Schatz, J. (2017). Übungsbuch Chemie für Mediziner. Berlin, Heidelberg: Springer.
Hitzenberger, J., Uhl, A., Schatz, J., & Drewello, T. (2017). Influence of electronic and molecular structure on the fragmentation dynamic of even-electron carbocationic triangulenes and helicenes in the gas phase. Journal of Mass Spectrometry. https://dx.doi.org/10.1002/jms.3912
Hoffmann, I., & Schatz, J. (2016). Microwave-mediated Newman-Kwart rearrangement in water. RSC Advances, 6, 80692 - 80699. https://dx.doi.org/10.1039/C6RA20676J
Schatz, J., Onodi, S., Hätzelt, A., & Gerke, T. (2016). Active ingredients which improve primary detergent power.
Schatz, J., Bartz, S., Schühle, D.T., & Peters, J.A. (2016). Highly selective naked-eye anion sensors based on thioureido or amido calix[4]arenes. Zeitschrift für Naturforschung Section B-A Journal of Chemical Sciences, 71(2), 113–118. https://dx.doi.org/10.1515/znb-2015-0146
Hoffmann, I., Blumenröder, B., Onodi, S., Dommer, S., & Schatz, J. (2015). Suzuki cross-coupling in aqueous media. Green Chemistry, 17(7), 3844-3857. https://dx.doi.org/10.1039/c5gc00794a
Tomasek, J., Seßler, M., Gröger, H., & Schatz, J. (2015). Olefin metathesis reaction in water and in air improved by supramolecular additive. Molecules, 20(10), 19130-19141. https://dx.doi.org/10.3390/molecules201019130
Schatz, J., & Hoffmann, I. (2015). Thiophene Metallation and Cross-Coupling Chemistry.
Tenbrink, K., Kemker, I., Schatz, J., & Gröger, H. (2014). Synthesis of substituted cycloalkene-1,1-dicarboxylates via olefin metathesis in water. Arkivoc, 2015(2), 10-19. https://dx.doi.org/10.3998/ark.5550190.p008.812
Hoffmann, I., & Schatz, J. (2013). Organometallic reactions in aqueous phase. Nachrichten aus der Chemie, 61, 748-753. https://dx.doi.org/10.1515/nachrchem.2013.61.7-8.748
Tomasek, J., & Schatz, J. (2013). Olefin metathesis in aqueous media. Green Chemistry, 15(9), 2317-2338. https://dx.doi.org/10.1039/c3gc41042k
Schatz, J., & Tammer, R. (2012). Erste Hilfe – Physik und Chemie für Mediziner [Elektronische Ressource] 2. korrigierte Auflage. Berlin, Heidelberg: Springer.
Borchert, S., Burda, E., Schatz, J., Hummel, W., & Gröger, H. (2012). Combination of a Suzuki cross-coupling reaction using a water-soluble palladium catalyst with an asymmetric enzymatic reduction towards a one-pot process in aqueous medium at room temperature. Journal of Molecular Catalysis B-Enzymatic, 84, 89-93. https://dx.doi.org/10.1016/j.molcatb.2012.03.006
Seßler, M., & Schatz, J. (2012). C-C couplings: Organometallic reactions in water. Chemie in Unserer Zeit, 46(1), 48-59. https://dx.doi.org/10.1002/ciuz.201200559
Tenbrink, K., Seßler, M., Schatz, J., & Gröger, H. (2011). Combination of olefin metathesis and enzymatic ester hydrolysis in aqueous media in a one-pot synthesis. Advanced Synthesis & Catalysis, 353(13), 2363-2367. https://dx.doi.org/10.1002/adsc.201100403
Schühle, D.T., Peters, J.A., & Schatz, J. (2011). Metal binding calixarenes with potential biomimetic and biomedical applications. Coordination Chemistry Reviews, 255, 2727-2745. https://dx.doi.org/10.1016/j.ccr.2011.04.005
Mohareb, R.M., & Schatz, J. (2011). Anti-tumor and anti-leishmanial evaluations of 1,3,4-oxadiazine, pyran derivatives derived from cross-coupling reactions of β-bromo-6H-1,3,4- oxadiazine derivatives. Bioorganic & Medicinal Chemistry, 19(8), 2707-2713. https://dx.doi.org/10.1016/j.bmc.2011.02.051
Schatz, J., & Seßler, M. (2011). Product Class 9.10.4: Thiophenes, Thiophene 1,1-Dioxides, and Thiopene 1-Oxides (update). Stuttgart, New York: Thieme Verlag.

Zuletzt aktualisiert 2018-16-08 um 23:50