Dr. Reiner Waibel



Organisationseinheit


Lehrstuhl für Pharmazeutische Chemie


Publikationen (Download BibTeX)

Go to first page Go to previous page 1 von 2 Go to next page Go to last page

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