Showing results 41 - 50 out of 380
2021
Seedorf, T., Kirschning, A., & Solga, D. (2021). Natural and Synthetic Oligoarylamides: Privileged Structures for Medical Applications. Chemistry - a European journal, 27(26), 7321-7339. https://doi.org/10.1002/chem.202005086
Kirschning, A. (2021). The coenzyme/protein pair and the molecular evolution of life. Natural product reports, 38(5), 993-1010. https://doi.org/10.1039/d0np00037j
Harms, V., Ravkina, V., & Kirschning, A. (2021). Mechanistic Similarities of Sesquiterpene Cyclases PenA, Omp6/7, and BcBOT2 Are Unraveled by an Unnatural "fPP-Ether" Derivative. Organic letters, 23(8), 3162-3166. https://doi.org/10.1021/acs.orglett.1c00882
George, V., & Kirschning, A. (2021). A Stable and Safe Form of Iodine Azide: Polymer-Bound Bisazidoiodate(I). SynOpen, 5(2), 104-107. https://doi.org/10.1055/a-1480-8983
Kösel, T., Dräger, G., & Kirschning, A. (2021). Oxidative azidations of phenols and ketones using iodine azide after release from an ion exchange resin. Organic & biomolecular
chemistry, 19(13), 2907-2911. https://doi.org/10.1039/d1ob00083g
Kirschning, A. (2021). Coenzymes and their role in the evolution of Life. Angewandte Chemie - International Edition, 60(12), 6242-6269. https://doi.org/10.1002/anie.201914786
Schulz, G., Victoria, C., Kirschning, A., & Steinmann, E. (2021). Rocaglamide and silvestrol: a long story from anti-tumor to anti-coronavirus compounds. Natural Product Reports, 38(1), 18-23. https://doi.org/10.1039/d0np00024h
2020
Oltmanns, M., & Kirschning, A. (2020). Subsupercritical Water Generated by Inductive Heating Inside Flow Reactors Facilitates the Claisen Rearrangement. SYNLETT, 31(19), 1942-1946. https://doi.org/10.1055/s-0040-1705945
Johannsmeier, S., Nguyen, M. T. T., Hohndorf, R., Dräger, G., Heinemann, D., Ripken, T., & Heisterkamp, A. (2020). PEGDMA Hydrogels for Cell Adhesion and Optical Waveguiding. ACS Applied Bio Materials, 3(10), 7011-7020. https://doi.org/10.1021/acsabm.0c00885
Wesemann, F., Heutling, A., Wienecke, P., & Kirschning, A. (2020). First ring-expanded maytansin lactone accessed by a new mutasynthetic variant. ChemBioChem, 21(20), 2927-2930. https://doi.org/10.1002/cbic.202000336, https://doi.org/10.15488/11033
