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Lars Hemmersbach

Lab 305 Tel +49 221 470 3059


[1] On the Diastereoselectivity of the Complexation of Ketopinic Acid-Derived 2-Acyloxy-1,3-cyclohexadienes and the Configurational Stability of Dienol-Fe(CO) 3 Complexes. A Case Study L. Hemmersbach, S. Romanski, S. Botov, A. Adler, J.-M. Neudörfl, H.-G. Schmalz, Organometallics 202140(16), 2909, 10.1021/acs.organomet.1c00354 

[2] Head‐to‐Head Comparison of Selected Extra‐ and Intracellular CO‐Releasing Molecules on Their CO‐Releasing and Anti‐Inflammatory Properties Y. Li, L. Hemmersbach, B. Krause, N. Sitnikov, A. Schlundt née Göderz, D. O. P. Maldonado, H.-G. Schmalz, B. Yard, ChemBioChem 2021, 23(1), e202100452, 10.1002/cbic.202100452

[3] An organometallic analogue of combretastatin A-4 and its apoptosis-inducing effects on lymphoma, leukemia and other tumor cells in vitro L. A. Onambele,   N. Hoffmann,  L. Kater,  L. Hemmersbach, J.-M. Neudörfl,   N. Sitnikov,  B. Kater,  C. Frias,  H.-G. Schmalz, A. Prokop, RSC Med. Chem. 202213, 1044, 10.1039/D2MD00144F

[4] Synthesis and Biological Evaluation of Water-Soluble Esterase-Activated CO-Releasing Molecules Targeting Mitochondria L. Hemmersbach, Y. Schreiner, X. Zhang, F. Dicke, L. Hünemeyer, J.-M. Neudörfl, T. Fleming, B. Yard, H.-G. Schmalz Chem. Eur. J. 2022, 28(50), e202201670, 10.1002/chem.202201670

[5] Vinylogous Winstein Rearrangement: Unexpected Isomerization of an Azide-Substituted Cyclohexadiene–Fe(CO)3 Complex A. Schlundt née Göderz, L. Hemmersbach, S. Romanski, J.-M. Neudörfl, H.-G. Schmalz Organometallics 2022, 41(21), 2997, 10.1021/acs.organomet.2c00418

[6] Studies Towards the Total Synthesis of Populusone: Stereoselective Construction of Functionalized 2-Oxa-bicyclo[2.2.2]octenes L. Hemmersbach, H.-G. Schmalz Synlett 2023, 34, 238, 10.1055/a-1983-1694

[7] Synthesis of Bifunctional Lipoxin-Derived Enzyme-Triggered CO-Releasing Molecules (LipET-CORMs) L. Hemmersbach, R. Adam, C. Plevnali, X. Zhang, B. Yard, H.-G. Schmalz Eur. J. Org. Chem. 202326(9), e202201424, 10.1002/ejoc.202201424