List of Publications Prof. Dr. Markus Kalesse
2019
Cordes, M. H. C., & Kalesse, M. (2019). The asymmetric vinylogous mukaiyama aldol reaction. Organic Reactions, 98, 173-774. https://doi.org/10.1002/0471264180.or098.02
Tungen, J. E., Gerstmann, L., Vik, A., De Matteis, R., Colas, R. A., Dalli, J., Chiang, N., Serhan, C. N., Kalesse, M., & Hansen, T. V. (2019). Resolving Inflammation: Synthesis, Configurational Assignment, and Biological Evaluations of RvD1n−3 DPA. Chemistry - a European journal, 25(6), 1476-1480. https://doi.org/10.1002/chem.201806029, https://doi.org/10.1002/chem.201901350
Lübken, D., Saxarra, M., & Kalesse, M. (2019). Tris(acetylacetonato) Iron(III): Recent Developments and Synthetic Applications. Synthesis (Germany), 51(1), 161-177. Article ss-2018-z0731-sr. https://doi.org/10.1055/s-0037-1610393, https://doi.org/10.15488/10508
2018
Brandt, C., Seja, P., Töllner, K., Römermann, K., Hampel, P., Kalesse, M., Kipper, A., Feit, P. W., Lykke, K., Toft-Bertelsen, T. L., Paavilainen, P., Spoljaric, I., Puskarjov, M., MacAulay, N., Kaila, K., & Löscher, W. (2018). Bumepamine, a brain-permeant benzylamine derivative of bumetanide, does not inhibit NKCC1 but is more potent to enhance phenobarbital's anti-seizure efficacy. NEUROPHARMACOLOGY, 143, 186-204. https://doi.org/10.1016/j.neuropharm.2018.09.025, https://doi.org/10.1016/j.neuropharm.2018.10.012
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
Lücke, D., Linne, Y., Hempel, K., & Kalesse, M. (2018). Total Synthesis of Pericoannosin A. Organic Letters, 20(15), 4475-4477. https://doi.org/10.1021/acs.orglett.8b01768
Surup, F., Kuhnert, E., Böhm, A., Pendzialek, T., Solga, D., Wiebach, V., Engler, H., Berkessel, A., Stadler, M., & Kalesse, M. (2018). The Rickiols: 20-, 22-, and 24-membered Macrolides from the Ascomycete Hypoxylon rickii. Chemistry - a European journal, 24(9), 2200-2213. https://doi.org/10.1002/chem.201704928
Li, J., Xing, J., Lücke, D., Lübken, D., Millbrodt, L., Plentz, R. R., & Kalesse, M. (2018). The Structure Elucidation of Haprolid. Synthesis (Germany), 50(3), 529-538. https://doi.org/10.1055/s-0036-1591836
2017
Witte, S. N. R., Hug, J. J., Géraldy, M. N. E., Müller, R., & Kalesse, M. (2017). Biosynthesis and Total Synthesis of Pyrronazol B: a Secondary Metabolite from Nannocystis pusilla. Chemistry - a European journal, 23(63), 15917-15921. https://doi.org/10.1002/chem.201703782
Poock, C., & Kalesse, M. (2017). Total Synthesis of Nannocystin Ax. Organic letters, 19(17), 4536-4539. https://doi.org/10.1021/acs.orglett.7b02112
