Zeige Ergebnisse 41 - 50 von 385
2021
Monsigny, L., Czarnocki, S., Sienkiewicz, M., Kopcha, W., Frankfurter, R., Vogt, C., Solodenko, W., Kajetanowicz, A., Kirschning, A., & Grela, K. (2021). Ruthenium Complex Bearing a Hydroxy Group Functionalised N-Heterocyclic Carbene Ligand: A Universal Platform for Synthesis of Tagged and Immobilised Catalysts for Olefin Metathesis. European Journal of Organic Chemistry, 2021(46), 6424-6434. https://doi.org/10.1002/ejoc.202101092
Ozkan, G., Stübler, A.-S., Aganovic, K., Dräger, G., Esatbeyoglu, T., & Capanoglu, E. (2021). Retention of polyphenols and vitamin C in cranberrybush purée (Viburnum opulus) by means of non-thermal treatments. Food Chemistry, 360, Artikel 129918. https://doi.org/10.1016/j.foodchem.2021.129918
Seemann, A., Panten, J., & Kirschning, A. (2021). Flow Chemistry under Extreme Conditions: Synthesis of Macrocycles with Musklike Olfactoric Properties. Journal of Organic Chemistry, 86(20), 13924-13933. https://doi.org/10.1021/acs.joc.1c00663
Banerjee, S., Szepes, M., Dibbert, N., Rios-Camacho, J.-C., Kirschning, A., Gruh, I., & Dräger, G. (2021). Dextran-based scaffolds for in-situ hydrogelation: Use for next generation of bioartificial cardiac tissues. Carbohydrate polymers, 262, Artikel 117924. https://doi.org/10.1016/j.carbpol.2021.117924
Kuhwald, C., & Kirschning, A. (2021). Matteson Reaction under Flow Conditions: Iterative Homologations of Terpenes. Organic letters, 23(11), 4300–4304. https://doi.org/10.1021/acs.orglett.1c01222
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
