Gesamtliste der Publikationen
Zeige Ergebnisse 371 - 380 von 955
2018
Werner, I., Heinisch, S. L., Nowik, I., Herber, R. H., & Butenschön, H. (2018). 1,16-Di-tert-butyl-1,16-diphospha[5.5]ferrocenophane: Synthesis, Reactions and Mössbauer Spectroscopy. ChemistrySelect, 3(46), 13132-13139. https://doi.org/10.1002/slct.201802793
Yue, Q., Stahl, F., Plettenburg, O., Kirschning, A., Warnecke, A., & Zeilinger, C. (2018). The Noncompetitive Effect of Gambogic Acid Displaces Fluorescence-Labeled ATP but Requires ATP for Binding to Hsp90/HtpG. Biochemistry, 57(18), 2601-2605. https://doi.org/10.1021/acs.biochem.8b00155
2017
Abdelhamid, I. A., Abdelmoniem, A. M., Fohrer, J., Bardenhorst, I., Wartchow, R., & Butenschön, H. (2017). Dianionic oxy-cope rearrangement with benzil derivatives: Meso-selective 3,3-coupling of two tetrahydrofuran moieties. European Journal of Organic Chemistry, 2017(46), 6951-6956. https://doi.org/10.1002/ejoc.201701397
Abdelmoniem, A. M., Ghozlan, S. A. S., Butenschön, H., & Abdelhamid, I. A. (2017). Facile Synthesis of 3-Amino-2,5-dihydropyridazines and 4-Deazatoxoflavin Analogues via [3 + 3] Atom Combination: Approaches to Pyridazine Incorporating Pyrazole Moiety. Journal of Heterocyclic Chemistry, 54(1), 473-479. https://doi.org/10.1002/jhet.2606
Ammermann, J., Schmidt, T., Donner, J., Reck, M., Dalton, M., Stumpp, N., Stiesch, M., Wagner-Döbler, I., & Kirschning, A. (2017). The carolactam strategy is ineffective: Synthesis and biological evaluation of carolactam. Organic and Biomolecular Chemistry, 15(40), 8553-8558. https://doi.org/10.1039/c7ob02060k
Butenschön, H. (2017). Nationalsozialistisches Unrecht an der TH Hannover: erster Bericht der Senatsarbeitsgruppe. Unimagazin: Forschungsmagazin der Leibniz Universität Hannover, (1), 26-28. https://www.uni-hannover.de/fileadmin/luh/content/alumni/unimagazin/2017_ns/unimagazin_17_1-2_200_neu_NS.pdf
Ceylan, S., Law, H. C. H., Kirschning, A., & Toy, P. H. (2017). Organocatalytic Alkyne Isomerizations under Flow Conditions Using Heterogeneous Bifunctional Polystyrene Bearing Phosphine and Phenol Groups. Synthesis (Germany), 49(1), 145-150. Artikel ss-2016-z0440-op. https://doi.org/10.1055/s-0036-1588589
Chen, W., Chen, R., Liu, Q., He, Y., He, K., Ding, X., Kang, L., Guo, X., Xie, N., Zhou, Y., Lu, Y., Cox, R. J., Molnár, I., Li, M., Shao, Y., & Chen, F. (2017). Orange, red, yellow: Biosynthesis of azaphilone pigments in Monascus fungi. Chemical science, 8(7), 4917-4925. https://doi.org/10.1039/c7sc00475c
Chen, X., Bui, K. C., Barat, S., Thi Nguyen, M. L., Bozko, P., Sipos, B., Kalesse, M., Malek, N. P., & Plentz, R. R. (2017). Therapeutic effects of Argyrin F in pancreatic adenocarcinoma. Cancer letters, 399, 20-28. https://doi.org/10.1016/j.canlet.2017.04.003
Codutti, L., Grimaldi, M., & Carlomagno, T. (2017). Structure-Based Design of Scaffolds Targeting PDE10A by INPHARMA-NMR. Journal of Chemical Information and Modeling, 57(6), 1488-1498. https://doi.org/10.1021/acs.jcim.7b00246
