Gesamtliste der Publikationen
Zeige Ergebnisse 361 - 370 von 959
2018
Oberhauser, C. M. (2018). Biotransformationen von Farnesylpyrophosphat-Analoga durch Sesquiterpencyclasen. [Dissertation, Gottfried Wilhelm Leibniz Universität Hannover]. Leibniz Universität Hannover. https://doi.org/10.15488/3944
Oberhauser, C., Harms, V., Seidel, K., Schröder, B., Ekramzadeh, K., Beutel, S., Winkler, S., Lauterbach, L., Dickschat, J. S., & Kirschning, A. (2018). Exploiting the Synthetic Potential of Sesquiterpene Cyclases for Generating Unnatural Terpenoids. Angewandte Chemie , 57(36), 11802-11806. https://doi.org/10.1002/anie.201805526, https://doi.org/10.1002/ange.201805526
Podrezova, E. V., Larkina, M. S., Belousov, M. V., Kirschning, A., Zhdankin, V. V., & Yusubov, M. S. (2018). Expedient synthesis of long-chain ω-substituted fatty acids and esters from cyclic ketones using iodine and hydrogen peroxide. Synthesis (Germany), 50(20), 4081-4088. https://doi.org/10.1055/s-0036-1591598
Ringel, M. T., Dräger, G., & Brüser, T. (2018). PvdO is required for the oxidation of dihydropyoverdine as the last step of fluorophore formation in Pseudomonas fluorescens. Journal of Biological Chemistry, 293(7), 2330-2341. https://doi.org/10.1074/jbc.RA117.000121
Schmiel, D., Gathy, R., & Butenschön, H. (2018). Cp∗Co(CO)I2 as Catalyst for Ortho-C,H Activation at Ferrocene: ODG-Dependent Preference for 2-Mono- or 2,5-Dialkenylation. Organometallics, 37(13), 2095-2110. https://doi.org/10.1021/acs.organomet.8b00243
Schor, R. (2018). Biosynthesis of xenovulenes in Acremonium strictum. [Dissertation, Gottfried Wilhelm Leibniz Universität Hannover]. Leibniz Universität Hannover. https://doi.org/10.15488/3173
Schor, R., & Cox, R. (2018). Classic fungal natural products in the genomic age: the molecular legacy of Harold Raistrick. Natural product reports, 35(3), 230-256. https://doi.org/10.1039/c8np00021b, https://doi.org/10.15488/3311
Schor, R., Schotte, C., Wibberg, D., Kalinowski, J., & Cox, R. J. (2018). Three previously unrecognised classes of biosynthetic enzymes revealed during the production of xenovulene A. Nature Communications, 9, Artikel 1963. Vorabveröffentlichung online. https://doi.org/10.1038/s41467-018-04364-9, https://doi.org/10.15488/3476
Schröder, B. (2018). Synthese unnatürlicher Farnesylderivate als Substrate für Sesquiterpenzyklasen: Mutasynthetischer Zugang zu heteroaromatischen Geldanamycin-Derivaten. [Dissertation, Gottfried Wilhelm Leibniz Universität Hannover]. Leibniz Universität Hannover. https://doi.org/10.15488/3259
Stempel, E., Kaml, R. F. X., Budisa, N., & Kalesse, M. (2018). Painting argyrins blue: Negishi cross-coupling for synthesis of deep-blue tryptophan analogue β-(1-azulenyl)-L alanine and its incorporation into argyrin C. Bioorganic and Medicinal Chemistry, 26(19), 5259-5269. https://doi.org/10.1016/j.bmc.2018.03.037
