M. Sc. Paul Eckhardt

 

Department of Chemistry
Johannes Gutenberg-University Mainz
Duesbergweg 10-14, 55128 Mainz
Room 2.223/02-125
Phone (06131) 39-25356
E-mail eckhardt[at]uni-mainz.de
Research interests: computational chemistry, 2-centered 3-electron bonds, natural product elucidation
Publications:

Pyrroloquinolones B–F: Five unusual alkaloids from Vernonia glabra (Steetz) Vatke (Asteraceae)

V. K. Takeuneu, P. Eckhardt, B. T. Tsafack, U. J. Tsopmene, B. K. Ponou, J. P. Dzoyem, R. B. Teponno, T. Opatz, L. A. Tapondjou, Phytochem., 2024, 220, 114010.

Two new steroids from the medicinal plant Physalis peruviana L.  

L. W. Demgne, P. Eckhardt, B. Y. Kianfé, R. T. Tchuenguem, J. P. Dzoyem, B. K. Ponou, R. B. Teponno, L. Barboni, T. Opatz, L. A. Tapondjou, Phytochem. Lett., 2024, 59, 5-9.

Discovery and characterization of a broderol-like illudin, Omphaderol in the mycelial extracts of Omphalotus mexicanus (Omphalotaceae) using UPLC-QTOF-MS and NMR spectroscopy

P. Eckhardt, S. Reinecke, T. Opatz, M. Stadler, B. Sandargo, Phytochem. Anal., 2023, 1-7.

A new phenolic glycoside from the leaves of Flacourtia flavescens Willd.

D. C. N. Jouogo, P. Eckhardt, J.-D.-D. Tamokou, G. M. Takongmo, L. Voutquenne-Nazabadioko, T. Opatz, L. A. Tapondjou, D. Ngnokam, R. B. Teponno, Nat. Prod. Res., 2023, 0, 1-11.

Substitution Effects on the Photophysical and Photoredox Properties of Tetraaza[7]helicenes

J. Rocker, J. A. Dresel, L. A. Krieger, P. Eckhardt, A. M. Ortuño, W. R. Kitzmann, G. H. Clever, K. Heinze, T. Opatz, Chem. Eur. J., 2023, 29, e2023012.

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.

Diplomeroterpenoid G: An unusual meroterpenoid from Mimosa pudica Linn. (Mimosaceae)

C. F. Kenmogne, P. Eckhardt, R. T. Tchuenguem, J. Groß, F. T. Ngouafong, B. K. Ponou, J. P. Dzoyem, R. B. Teponno, T. Opatz, L. A. Tapondjou, Tetrahedron, 2023, 120, 154451.

Two Paths to Oxidative C−H Amination Under Basic Conditions: A Theoretical Case Study Reveals Hidden Opportunities Provided by Electron Upconversion

P. Eckhardt, Q. Elliott, I. Alabugin, T. Opatz, Chem. Eur. J., 2022, 28, e202201637.

Constituents of Desmodium salicifolium (Poir.) DC (Fabaceae) with antifungal activity

A. P. T. Donkia, P. Eckhardt, B. T. Tsafack , R. T. Tchuenguem, J. Groß, B. K. Ponou, R. B. Teponno, J. P. Dzoyem, T. Opatz, L. Barboni, L. A. Tapondjou, Phytochem. Lett., 2022, 50, 100-105.

Muellerilactone and other bioactive constituents of Phyllanthus muellerianus (kuntze) exell

B. Tsakem, P. Eckhardt, R. T. Tchuenguem, B. K. Ponou, J. P. Dzoyem, R. B. Teponno, T. Opatz, L. Barboni, L. A. Tapondjou, Biochem. Syst. Ecol., 2022, 101, 104397.

A dinorcassane-type diterpene and a steroidal saponin from Distemonanthus benthamianus Baill. (Caesalpiniaceae)

R. V. K. Tchebou, P. Eckhardt, B. M. Kemkuignou, R. Tchuenguem, R. T. Fouedjou, B. K. Ponou, J. P. Dzoyem, R. B. Teponno, L. Barboni, T. Opatz, L. A. Tapondjou, Phytochem. Lett., 2022, 48, 62-67.

An insight into the synthesis of N-methylated polypeptides

J. Groß, , Polym. Chem., 2020, 11, 6919-6927.