skip to content

Dr. Dominik Albat

Lab 322 Tel +49 221 470 6821
e-mail

Publications

[1] Total Synthesis of alpha-Tocopherol through Enantioselective Iridium-Catalyzed Fragmentation of a Spiro-Cyclobutanol Intermediate, F. Ratsch, W. Schlundt, D. Albat, A. Zimmer, J. M. Neudorfl, T. Netscher, H. G. Schmalz, Chem. Eur. J., 201925 (19), 4941. 10.1002/chem.201900564

[2] Pd-catalyzed asymmetric N-allylation of amino acid esters with exceptional levels of catalyst control: Stereo-divergent synthesis of ProM-15 and related bicyclic dipeptide mimetics, S. Dohmen, M. Reiher, D. Albat, S. Akyol, M. Barone, J.-M. Neudoerfl, R. Kuehne, H.-G. Schmalz, Chem. Eur. J. 202026 (14), 3049, 10.1002/chem.202000307

[3] Designed nanomolar small-molecule inhibitors of Ena/VASP EVH1 interaction impair invasion and extravasation of breast cancer cells, M. Barone, M. Müller, S. Chiha, J. Ren, D. Albat, A. Soicke, S. Dohmen, M. Klein, J. Bruns, M. van Dinther, R. Opitz, P. Lindemann, M. Beerbaum, K. Motzny, Y. Roske, P. Schmieder, R. Volkmer, M. Nazaré, U. Heinemann, H. Oschkinat, P. ten Dijke, H.-G-Schmalz, R. Kühne, PNAS 2020117 (47), 29684, 10.1073/pnas.2007213117

[4] A Short Enantioselective Synthesis of (S)-Levetiracetam through Direct Palladium-Catalyzed Asymmetric N-Allylation of Methyl 4-Aminobutyrate, D. Albat, J.-M. Neudörfl, H.-G. Schmalz, Synlett 202132 (11), 1089, 10.1055/a-1493-9078

[5] A General Stereocontrolled Synthesis of Opines via Asymmetric Pd‐Catalyzed N‐Allylation of Amino Acid Esters, D. Albat, J.-M. Neudörfl, H.-G. Schmalz, Eur. J. Org. Chem. 2021, (14), 2099, 10.1002/ejoc.202100259

[6] Improved Synthesis of MediPhos Ligands and their Use in the Pd-catalyzed Enantioselective N-Allylation of Glycine Esters, D. Albat, M. Reiher, J.-M. Neudörfl, H.-G. Schmalz Eur. J. Org. Chem. 2021, Accepted Article10.1002/ejoc.202100748

[7] On the Asymmetric Ir‐catalyzed N‐Allylation of Amino Acid Esters: Improved Selectivities through Structural Variation of the Chiral Phosphoramidite Ligand D. Albat, A. Köcher, J. Witt, H.-G. Schmalz, Eur. J. Org. Chem. 2022, (12), e202200188, 10.1002/ejoc.202200188