2023
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
Linne, Y., Lücke, D., Gerdes, K., Bajerke, K., & Kalesse, M. (Angenommen/Im Druck). Stereoselective Synthesis of Allylic Alcohols via Substrate Control on Asymmetric Lithiation. Chemistry - a European journal. https://doi.org/10.1002/chem.202302699
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, [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), [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
Lücke, D., & Kalesse, M. (2022). Chiral Polyoxygenated Tertiary Alcohols through Kiyooka Aldol Reaction. SYNLETT, 33(12), 1117-1122. https://doi.org/10.1055/a-1775-7590
Sara, A. A., Um-E-Farwa, U. E. F., Saeed, A., & Kalesse, M. (2022). Recent Applications of the Diels-Alder Reaction in the Synthesis of Natural Products (2017-2020). Synthesis (Germany), 54(4), 975-998. [ss-2021-r0249-st]. https://doi.org/10.1055/a-1532-4763
2021
Eggert, A., Etling, C., Millbrodt, L., Schulz, G., & Kalesse, M. (2021). Oxazaborolidinone-Mediated Asymmetric Bisvinylogous Mukaiyama Aldol Reaction. Organic letters, 23(22), 8722-8726. https://doi.org/10.1021/acs.orglett.1c03165
