Gesamtliste der Publikationen
Zeige Ergebnisse 381 - 390 von 959
2017
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
Dickerhoff, J., Haase, L., Langel, W., & Weisz, K. (2017). Tracing Effects of Fluorine Substitutions on G-Quadruplex Conformational Changes. ACS chemical biology, 12(5), 1308-1315. https://doi.org/10.1021/acschembio.6b01096
Donner, J., Reck, M., Bunk, B., Jarek, M., App, C. B., Meier-Kolthoff, J. P., Overmann, J., Müller, R., Kirschning, A., & Wagner-Döbler, I. (2017). The biofilm inhibitor carolacton enters Gram-negative cells: Studies using a Tol-Cdeficient strain of Escherichia coli. mSphere, 2(5), Artikel e00375-17. https://doi.org/10.1128/mspheredirect.00375-17
Dziechciejewski, W. J. (2017). Asymmetrische Rh(I)-katalysierte 1,4-Addition von Arylboronsäuren an acceptorsubstituierte carbo- und heterocyclische Cycloalkene: formale Synthese von (+)-Vabicaserin = Asymmetric rhodium(I)-catalyzed 1,4-addition of arylboronic acids to acceptor substituted carbo- und heterocyclic cycloalkenes ; formal synthesis of (+)-Vabicaserin. [Dissertation, Gottfried Wilhelm Leibniz Universität Hannover]. Leibniz Universität Hannover. https://doi.org/10.15488/8962
Essoung, F. R. E., Mba'ning, B. M., Lwande, W., Ngouela, S. A., Tsamo, E., Chhabra, S. C., Hassanali, A., & Cox, R. J. (2017). Welwitschianalol A and B, two cyclohexene derivatives and other insecticidal constituents of Caesalpinia welwitschiana (Oliv.) Brenan. Phytochemistry letters, 22, 81-86. https://doi.org/10.1016/j.phytol.2017.09.010
Feng, J., Zhang, P., Cui, Y., Li, K., Qiao, X., Zhang, Y. T., Li, S. M., Cox, R. J., Wu, B., Ye, M., & Yin, W. B. (2017). Regio- and Stereospecific O-Glycosylation of Phenolic Compounds Catalyzed by a Fungal Glycosyltransferase from Mucor hiemalis. Advanced Synthesis and Catalysis, 359(6), 995-1006. https://doi.org/10.1002/adsc.201601317, https://doi.org/10.1002/adsc.201701070
Gao, S. S., Wang, L., Song, Z., Hothersall, J., Stevens, E. R., Connolly, J., Winn, P. J., Cox, R. J., Crump, M. P., Race, P. R., Thomas, C. M., Simpson, T. J., & Willis, C. L. (2017). Selected Mutations Reveal New Intermediates in the Biosynthesis of Mupirocin and the Thiomarinol Antibiotics. Angewandte Chemie , 56(14), 3930-3934. https://doi.org/10.1002/anie.201611590, https://doi.org/10.1002/ange.201611590
