Dr. Stefan Pusch


Institute of Organic Chemistry
Johannes Gutenberg-University Mainz
Duesbergweg 10-14, 55128 Mainz
Room 2.223/02-125
Phone (06131) 39-25356
E-mail stefan.pusch[at]uni-mainz.de
Research interests: Computational chemistry, Photochemistry, Mechanistic studies, N-Heterocycles

Comparison of Different Density Functional Theory Methods for the Calculation of Vibrational Circular Dichroism Spectra

J. Groß, J. Kühlborn, S. Pusch, C. Weber, L. Andernach, G. Renzer, P. Eckhardt, J. Brauer, T. Opatz, Chirality, 2023, 1-13.

Visible Light-Induced Sulfonylation/Arylation of Styrenes in a Double Radical Three-Component Photoredox Reaction
B. Lipp, L. M. Kammer, M. Kücükdisli, A. Luque, J. Kühlborn,
S. Pusch, G. Matulevičiūtė, D. Schollmeyer, A. Šačkus, T. Opatz, Chem. Eur. J. 2019, 8965–8969.
(Hot Paper) (cover picture)

Mechanism and cis/trans Selectivity of Vinylogous Nazarov-Type [6π] Photocyclizations
S. Pusch, A. Tröster, D. Lefrancois, P. Farahani, A. Dreuw, T. Bach, T. Opatz, J. Org. Chem. 2018, 83, 964–972.

Synthesis and Unusual NMR-Spectroscopic Behavior of a Strained Bicyclic Ammonium Salt
S. Pusch, D. Schollmeyer, T. Opatz, Eur. J. Org. Chem. 2018, 1204-1207. (Cover picture)

Oxidation of Trialkylamines by BrCCl3—Scope, Applications and Mechanistic Aspects
A. M. Nauth, J. C. Orejarena Pacheco, S. Pusch, T. Opatz, Eur. J. Org. Chem. 2017, 6966–6974.

Polyethylene bio-degradation by caterpillars?
C. Weber, S. Pusch, T. Opatz, Curr. Biol. 2017, 27, R744-R745.

Haloperoxidase mimicry by CeO2-x nanorods combats biofouling
K. Herget. P. Hubach, S. Pusch, P. Deglmann, H. Götz, T. E. Gorelik, I. A. Gural'skiy, F. Pfitzner, T. Link, S. Schenk, M. Panthöfer, V. Ksenofontov, U. Kolb, T. Opatz, R. André, W. Tremel
Adv. Mater. 2017, 29, 1603823.

Characterization of the synthetic cannabinoid MDMB-CHMCZCA
Carina Weber, Stefan Pusch, Dieter Schollmeyer, Sascha Münster-Müller, Michael Pütz and Till Opatz
Beilstein J. Org. Chem. 2016, 12, 2808–2815.

Absolute Configuration Determination of 2,3-Dihydro-1H,5H-pyrazolo-[1,2-a]pyrazoles using Chiroptical Methods at Different Wavelengths.
Eva Pušavec Kirar, Uroš Grošelj, Amalija Golobič, Franc Požgan, Stefan Pusch, Carina Weber, Lars Andernach, Bogdan Štefane, Till Opatz, Jurij Svete
J. Org. Chem. 2016, 81, 11802–11812.

A Light-Induced Vinylogous Nazarov-Type Cyclization
S. Pusch, D. Schollmeyer, T. Opatz
Org. Lett. 2016, 18, 3043-3045.

Absolute configuration of the synthetic cannabinoid MDMB-CHMICA with its chemical characteristics in illegal products
L. Andernach, S. Pusch, C. Weber, D. Schollmeyer, S. Münster-Müller, M. Pütz, T. Opatz, Forensic Toxicol. 2016, 34, 344-352.

A Photoinduced Cobalt-Catalyzed Synthesis of Pyrroles through In-Situ Generated Acylazirines
S. Pusch, D. Kowalczyk, T. Opatz, J. Org. Chem. 2016, 81, 4170-4178.

A Photochemical One-Pot Three-Component Synthesis of Tetrasubstituted Imidazoles
S. Pusch, T. Opatz, Org. Lett. 2014, 16, 5430-5433.