Sebastian Keess
Affiliations: | 2014- | Technische Universität Berlin, Berlin, Berlin, Germany |
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Publications
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| Gesmundo NJ, Rago AJ, Young JM, et al. (2024) At the Speed of Light: The Systematic Implementation of Photoredox Cross-Coupling Reactions for Medicinal Chemistry Research. The Journal of Organic Chemistry |
| Dong W, Keess S, Molander GA. (2023) Nickel-Mediated Alkyl-, Acyl-, and Sulfonylcyanation of [1.1.1]Propellane. Chem Catalysis. 3 |
| Levitre G, Keess S, Molander GA. (2023) Photoinduced Diastereoselective Aminoalkylation of Cubanes. Organic Letters |
| Fernández DF, González-Esguevillas M, Keess S, et al. (2023) Redefining the Synthetic Logic of Medicinal Chemistry. Photoredox-Catalyzed Reactions as a General Tool for Aliphatic Core Functionalization. Organic Letters |
| Huang W, Keess S, Molander GA. (2023) A General and Practical Route to Functionalized Bicyclo[1.1.1]Pentane-Heteroaryls Enabled by Photocatalytic Multicomponent Heteroarylation of [1.1.1]Propellane. Angewandte Chemie (International Ed. in English). e202302223 |
| Huang W, Zheng Y, Keess S, et al. (2023) A General and Modular Approach to BCP Alkylamines via Multicomponent Difunctionalization of [1.1.1]Propellane. Journal of the American Chemical Society. 145: 5363-5369 |
| Zheng Y, Huang W, Dhungana RK, et al. (2022) Photochemical Intermolecular [3σ + 2σ]-Cycloaddition for the Construction of Aminobicyclo[3.1.1]heptanes. Journal of the American Chemical Society. 144: 23685-23690 |
| Huang W, Keess S, Molander GA. (2022) One step synthesis of unsymmetrical 1,3-disubstituted BCP ketones nickel/photoredox-catalyzed [1.1.1]propellane multicomponent dicarbofunctionalization. Chemical Science. 13: 11936-11942 |
| Huang W, Keess S, Molander GA. (2022) Dicarbofunctionalization of [1.1.1]Propellane Enabled by Nickel/Photoredox Dual Catalysis: One-Step Multicomponent Strategy for the Synthesis of BCP-Aryl Derivatives. Journal of the American Chemical Society |
| Polites VC, Badir SO, Keess S, et al. (2021) Nickel-Catalyzed Decarboxylative Cross-Coupling of Bicyclo[1.1.1]pentyl Radicals Enabled by Electron Donor-Acceptor Complex Photoactivation. Organic Letters |