Showing results 1 - 10 out of 148
2024
Eggert, A., Schuppe, K. T., Fuchs, H. L. S., Brönstrup, M., & Kalesse, M. (2024). Total Synthesis of Acanthodoral Using a Rearrangement Strategy. Organic letters, 26(15), 2893-2896. https://doi.org/10.1021/acs.orglett.3c03717
Lücke, D., & Kalesse, M. (2024). Development of the Synthesis of Desepoxy-Tedanolide C. Journal of Organic Chemistry, 89(4), 2408–2430. https://doi.org/10.1021/acs.joc.3c02437
Linne, Y., Lücke, D., Gerdes, K., Bajerke, K., & Kalesse, M. (2024). Stereoselective Synthesis of Allylic Alcohols via Substrate Control on Asymmetric Lithiation. Chemistry - a European journal, 30(3), Article e202302699. https://doi.org/10.1002/chem.202302699
2023
Kalesse, M., & Linne, E. (2023). Stereoselective Construction of β-chiral Homoallyl Functionalities by Substrate- and Reagent-Controlled Iterative 1,2-Metallate Rearrangements. Organic letters, 25(46), 8210-8214. https://doi.org/10.1021/acs.orglett.3c02935
Linne, Y., Lohrberg, D., Struwe, H., Linne, E., Stohwasser, A., & Kalesse, M. (2023). 1,2-Metallate Rearrangement as a Toolbox for the Synthesis of Allylic Alcohols. Journal of Organic Chemistry, 88(17), 12623–12629. https://doi.org/10.1021/acs.joc.3c01309
Linne, Y., Birkner, M., Flormann, J., Lücke, D., Becker, J. A., & Kalesse, M. (2023). Sparteine-Free, Highly Stereoselective Construction of Complex Allylic Alcohols Using 1,2-Metallate Rearrangements. JACS Au, 3(6), 1695-1710. https://doi.org/10.1021/jacsau.3c00114
Etling, C., Tedesco, G., Di Marco, A., & Kalesse, M. (2023). Asymmetric Total Synthesis of Illisimonin A. Journal of the American Chemical Society, 145(12), 7021-7029. https://doi.org/10.1021/jacs.3c01262
2022
Borgert, S. R., Henke, S., Witzgall, F., Schmelz, S., zur Lage, S., Hotop, S. K., Stephen, S., Lübken, D., Krüger, J., Gomez, N. O., van Ham, M., Jänsch, L., Kalesse, M., Pich, A., Brönstrup, M., Häussler, S., & Blankenfeldt, W. (2022). An enzyme moonlights as a chaperone to control virulence of Pseudomonas aeruginosa. Nature Communications, 13, Article 7402. https://doi.org/10.21203/rs.3.rs-1489597/v1, https://doi.org/10.1038/s41467-022-35030-w
Lübken, D., Siekmeyer, B., & Kalesse, M. (2022). Photochemical 1,3-Acyl Shifts in Natural Product Synthesis. European Journal of Organic Chemistry, 2022(41), Article e202200701. https://doi.org/10.1002/ejoc.202200701
Siekmeyer, B., Lübken, D., Bajerke, K., Bernhardt, B., Schreiner, P. R., & Kalesse, M. (2022). Total Synthesis of (-)-Antroalbocin A Enabled by a Strain Release-Controlled Photochemical 1,3-Acyl Shift. Organic letters, 24(31), 5812-5816. https://doi.org/10.26434/chemrxiv-2021-3pd4x, https://doi.org/10.1021/acs.orglett.2c02347
