Lukas Rycek
Affiliations: | Department of Organic Chemistry, Faculty of Science, Charles University |
Area:
Organic, organometallic chemistryGoogle:
"Lukas Rycek"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Marko Mihovilovic | grad student | 2011-2015 | Vienna University of Technology |
| Martin Kotora | grad student | 2019-2020 | Charles University, Prague Czech Republic |
| Tomas Hudlicky | post-doc | 2015-2017 | Brock University (Canada) |
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Publications
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| Rycek L, Mateus M, Beytlerová N, et al. (2021) Catalytic Cyclotrimerization Pathway for Synthesis of Selaginpulvilins C and D: Scope and Limitations. Organic Letters |
| Makarova M, Rycek L, Hajicek J, et al. (2019) Tetrodotoxin: History, Biology, and Synthesis. Angewandte Chemie (International Ed. in English) |
| Rycek L, Ticli V, Pyszkowski J, et al. (2018) Stereoselective Synthesis of the Isomers of Notoincisol A: Assigment of the Absolute Configuration of this Natural Product and Biological Evaluation. Journal of Natural Products |
| Dreier D, Resetar M, Temml V, et al. (2018) Magnolol dimer-derived fragments as PPARγ-selective probes. Organic & Biomolecular Chemistry |
| Baidilov D, Rycek L, Trant JF, et al. (2018) Chemoenzymatic Approach to Tetrodotoxin: Synthesis of Fukuyama's, Alonso's, and Sato's Advanced Intermediates. Angewandte Chemie (International Ed. in English) |
| Dreier D, Latkolik S, Rycek L, et al. (2017) Linked magnolol dimer as a selective PPARγ agonist - Structure-based rational design, synthesis, and bioactivity evaluation. Scientific Reports. 7: 13002 |
| Rycek L, Hudlicky T. (2017) Applications of the Wittig-Still rearrangement in organic synthesis. Angewandte Chemie (International Ed. in English) |
| Rycek L, Hayward JJ, Latif MA, et al. (2016) Chemoenzymatic total synthesis of hydromorphone by an oxidative dearomatization/intramolecular [4+2] cycloaddition sequence: a 2nd generation approach. The Journal of Organic Chemistry |
| Rycek L, Puthenkalam R, Schnürch M, et al. (2015) Corrigendum to "Metal-assisted synthesis of unsymmetrical magnolol and honokiol analogs and their biological assessment as GABAA receptor ligands" [Bioorg. Med. Chem. Lett. 25/2 (2015) 400-403]. Bioorganic & Medicinal Chemistry Letters. 25: 1811 |
| Rycek L, Puthenkalam R, Schnürch M, et al. (2015) Metal-assisted synthesis of unsymmetrical magnolol and honokiol analogs and their biological assessment as GABAA receptor ligands. Bioorganic & Medicinal Chemistry Letters. 25: 400-3 |