Dr. Reiner Waibel


Lehrstuhl für Pharmazeutische Chemie

Publikationen (Download BibTeX)

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Lampros, M., Brox, R., Frank, T., Poklukar, G., Palmisano, R., Waibel, R.,... Tschammer, N. (2016). Discovery and Characterization of Biased Allosteric Agonists of the Chemokine Receptor CXCR3. Journal of medicinal chemistry, 59(5), 2222-43. https://dx.doi.org/10.1021/acs.jmedchem.5b01965
Röhrig, W., Waibel, R., Perlwitz, C., Pischetsrieder, M., & Hoch, T. (2016). Identification of the oleic acide ethanolamide (OEA) isomer cis-vaccenic acid ethanolamide (VEA) as a highly abundant 18:1 fatty acid ethanolamide in blood plasma from rats and humans. Analytical and Bioanalytical Chemistry, 408(22), 6141-6151. https://dx.doi.org/10.1007/s00216-016-9720-8
Maia de Pádua, R., Meitinger, N., Hennemann, M., Schebitz, P., Waibel, R., Löber, S.,... Kreis, W. (2016). Spontaneous butenolide ring formation of pregnane-21-O-malonyl hemiesters under mild reaction conditions is facilitated by the 14β-hydroxy group present in all natural cardenolides. Tetrahedron, 72, 4556-4563. https://dx.doi.org/10.1016/j.tet.2016.06.024
Gensberger, S., Knabner, C., Waibel, R., Huppert, J., & Pischetsrieder, M. (2015). Qualitative profiling of polyglucose degradation products in peritoneal dialysis fluids. Analytical Chemistry, 87, 6103-6111. https://dx.doi.org/10.1021/acs.analchem.5b00665
Maia de Pádua, R., Meitinger, N., de Souza Filho, J.D., Waibel, R., Gmeiner, P., Braga, F.C., & Kreis, W. (2012). Biotransformation of 21-O-acetyl-deoxycorticosterone by cell suspension cultures of Digitalis lanata (strain W.1.4). Steroids, 77(13), 1373-1380. https://dx.doi.org/10.1016/j.steroids.2012.07.016
Wakchaure, S., Einsiedel, J., Waibel, R., & Gmeiner, P. (2012). Conformationally restricted peptide mimetics by ring-closing olefin metathesis. Synthesis-Stuttgart, 44(17), 2682-2694. https://dx.doi.org/10.1055/s-0032-1316758
Pinsker, A., Einsiedel, J., Härterich, S., Waibel, R., & Gmeiner, P. (2011). A highly efficient type I β-turn mimetic simulating an asx-pro-turn-like structure. Organic Letters, 13(13), 3502-3505. https://dx.doi.org/10.1021/ol201313q
Paul, A., Einsiedel, J., Waibel, R., Heinemann, F., Meyer, K., & Gmeiner, P. (2009). Novel triazolopeptides: chirospecific synthesis and conformational studies of proline derived analogs. Tetrahedron, 65(31), 6156-6168. https://dx.doi.org/10.1016/j.tet.2009.05.045
Maia de Pádua, R., Waibel, R., Kuate, S.P., Schebitz, P., Hahn, S., Gmeiner, P., & Kreis, W. (2008). A simple chemical method for synthesizing malonyl hemiesters of 21-hydroxy-pregnanes, potential intermediates in cardenolide biosynthesis. Steroids, 73(4), 458-465. https://dx.doi.org/10.1016/j.steroids.2007.12.012
Einsiedel, J., Lanig, H., Waibel, R., & Gmeiner, P. (2007). Molecular Building Kit of Fused-Proline-Derived Peptide Mimetics Allowing Specific Adjustment of the Dihedral Psi Angle. Journal of Organic Chemistry, 72, 9102-9113. https://dx.doi.org/10.1021/jo701703e

Zuletzt aktualisiert 2017-02-04 um 02:01