Publikationen der Arbeitsgruppe Naturstoffchemie

Zeige Ergebnisse 101 - 110 von 148

2006


Ehrlich, G., Hassfeld, J., Eggert, U., & Kalesse, M. (2006). The total synthesis of (+)-tedanolide. Journal of the American Chemical Society, 128(43), 14038-14039. https://doi.org/10.1021/ja0659572
Stelmakh, A., Stellfeld, T., & Kalesse, M. (2006). Tandem intramolecular Michael-Aldol reaction as a tool for the construction of the C-ring of hexacyclinic acid. Organic letters, 8(16), 3485-3488. https://doi.org/10.1021/ol061096q
Liesener, F. P., Jannsen, U., & Kalesse, M. (2006). Synthesis of the northern hemisphere of amphidinolide H2. Synthesis, (15), 2590-2602. https://doi.org/10.1055/s-2006-942459
Raghunathan, D., Sánchez-Pedregal, V. M., Junker, J., Schwiegk, C., Kalesse, M., Kirschning, A., & Carlomagno, T. (2006). TAR-RNA recognition by a novel cyclic aminoglycoside analogue. Nucleic Acids Research, 34(12), 3599-3608. https://doi.org/10.1093/nar/gkl494

2005


Liesener, F. P., & Kalesse, M. (2005). Synthesis of the C19-C26 segment of amphidinolide H2. SYNLETT, (14), 2236-2238. https://doi.org/10.1055/s-2005-872236
Hassfeld, J., Kalesse, M., Stellfeld, T., & Christmann, M. (2005). Asymmetric total synthesis of complex marine natural products. In R. Ulber, & Y. Le Gal (Hrsg.), Marine Biotechnology II (S. 133-203). (Advances in Biochemical Engineering/Biotechnology; Band 97). https://doi.org/10.1007/b135825
Hassfeld, J., Eggert, U., & Kalesse, M. (2005). Synthesis of the C1-C17 macrolactone of tedanolide. Synthesis, (7), 1183-1199. https://doi.org/10.1055/s-2005-865302
Rahn, N., & Kalesse, M. (2005). A one-pot non-aldol-aldol vinylogous Mukaiyama aldol tandem sequence for the rapid construction of polyketide frameworks. SYNLETT, (5), 863-865. https://doi.org/10.1055/s-2005-863743
Ehrlich, G., & Kalesse, M. (2005). Synthesis of the C13-C23 segment of tedanolide. SYNLETT, (4), 655-657. https://doi.org/10.1055/s-2005-862391
Kalesse, M. (2005). Recent advances in vinylogous aldol reactions and their applications in the syntheses of natural products. In J. Mulzer (Hrsg.), Natural Product Synthesis II: Targets, Methods, Concepts (S. 43-76). (Topics in Current Chemistry; Band 244). https://doi.org/10.1007/b96887