Publikationsliste Prof. Dr. Markus Kalesse
Zeige Ergebnisse 81 - 90 von 148
2010
Stauch, B., Simon, B., Basile, T., Schneider, G., Malek, N. P., Kalesse, M., & Carlomagno, T. (2010). Elucidation of the structure and intermolecular interactions of a reversible cyclic-peptide inhibitor of the proteasome by NMR spectroscopy and molecular modeling. Angewandte Chemie - International Edition, 49(23), 3934-3938. https://doi.org/10.1002/anie.201000140
Eggert, U., Nisar, M., Girbig, A.-K., Markus, K., Bulow, L., Frank, R., Ronald, F., Nisar, M., Andreas, R., Anna-Katharina, G., Leila, B., Ulrike, E., Tobias, B., Markus, K., Brodmann, T., & Rentsch, A. (2010). Method for producing intermediates for the production of novel macrocycles that are inhibitors of the proteasomic degradation of p27, such as argyrin and derivatives thereof, and uses of said macrocycles. (Patent Nr. AU2009270571).
Rand, K., Noll, C., Schiebel, H. M., Kemken, D., Dülcks, T., Kalesse, M., Heinz, D. W., & Layer, G. (2010). The oxygen-independent coproporphyrinogen III oxidase HemN utilizes harderoporphyrinogen as a reaction intermediate during conversion of coproporphyrinogen III to protoporphyrinogen IX. Biological chemistry, 391(1), 55-63. https://doi.org/10.1515/BC.2010.006
Landsberg, D., & Kalesse, M. (2010). Synthesis of symmetrical ureas by (Diacetoxyiodo)benzene-induced hofmann rearrangement. SYNLETT, (7), 1104-1106. https://doi.org/10.1055/s-0029-1219566
2009
Simsek, S., & Kalesse, M. (2009). Enantioselective synthesis of polyketide segments through vinylogous Mukaiyama aldol reactions. Tetrahedron letters, 50(26), 3485-3488. https://doi.org/10.1016/j.tetlet.2009.03.013
Hagelueken, G., Albrecht, S. C., Steinmetz, H., Jansen, R., Heinz, D. W., Kalesse, M., & Schubert, W. D. (2009). The absolute configuration of rhizopodin and its inhibition of actin polymerization by dimerization. Angewandte Chemie - International Edition, 48(3), 595-598. https://doi.org/10.1002/anie.200802915
Brodmann, T., Lorenz, M., Schäckel, R., Simsek, S., & Kalesse, M. (2009). Highly stereoselective aldol reactions in the total syntheses of complex natural products. SYNLETT, (2), 174-192. https://doi.org/10.1055/s-0028-1087520
Lorenz, M., Bluhm, N., & Kalesse, M. (2009). Studies on the C22-C23 aldol coupling of spirangien. Synthesis, (18), 3061-3066. https://doi.org/10.1055/s-0029-1216918
2008
Schübel, N., Roy, M., & Kalesse, M. (2008). Syntheses of the tedanolides and myriaporones. Comptes rendus chimie, 11(11-12), 1419-1446. https://doi.org/10.1016/j.crci.2008.05.013
Eggert, U., Diestel, R., Sasse, F., Jansen, R., Kunze, B., & Kalesse, M. (2008). Chondramide C: Synthesis, configurational assignment, and structure-activity relationship studies. Angewandte Chemie - International Edition, 47(34), 6478-6482. https://doi.org/10.1002/anie.200801156
