Michael Smietana
Affiliations: | University of Montpellier, Montpellier, Occitanie, France |
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Parents
Sign in to add mentor| Charles Mioskowski | grad student | 2001 | University of Strasbourg |
| Eric T. Kool | post-doc | 2002-2004 | Stanford |
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Publications
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| Oger S, Duchemin N, Bendiab YM, et al. (2023) Expanding the 'aplysinospin cascade' through DNA-templated [2+2] photocycloaddition. Chemical Communications (Cambridge, England) |
| Duchemin N, Aubert S, de Souza JV, et al. (2022) New Benchmark in DNA-Based Asymmetric Catalysis: Prevalence of Modified DNA/RNA Hybrid Systems. Jacs Au. 2: 1910-1917 |
| Duchemin N, Cattoen M, Gayraud O, et al. (2020) Direct Access to Highly Enantioenriched α-Branched Acrylonitriles through a One-Pot Sequential Asymmetric Michael Addition/Retro-Dieckmann/Retro-Michael Fragmentation Cascade. Organic Letters. 22: 5995-6000 |
| Debiais M, Lelievre A, Smietana M, et al. (2020) Splitting aptamers and nucleic acid enzymes for the development of advanced biosensors. Nucleic Acids Research. 48: 3400-3422 |
| Clavé G, Dursun E, Vasseur JJ, et al. (2020) An Entry of the Chemoselective Sulfo-Click Reaction into the Sphere of Nucleic Acids. Organic Letters. 22: 1914-1918 |
| Mansot J, Lauberteaux J, Lebrun A, et al. (2020) DNA-Based Asymmetric Inverse Electron-Demand Hetero-Diels-Alder. Chemistry (Weinheim An Der Bergstrasse, Germany). 26: 3519-3523 |
| Debiais M, Vasseur J, Müller S, et al. (2020) Selective Chemical Modification of DNA with Boronic Acids by On-Column CuAAc Reactions Synthesis |
| Larcher A, Nocentini A, Supuran CT, et al. (2019) Bis-benzoxaboroles: Design, Synthesis, and Biological Evaluation as Carbonic Anhydrase Inhibitors. Acs Medicinal Chemistry Letters. 10: 1205-1210 |
| Mansot J, Aubert S, Duchemin N, et al. (2019) A rational quest for selectivity through precise ligand-positioning in tandem DNA-catalysed Friedel-Crafts alkylation/asymmetric protonation. Chemical Science. 10: 2875-2881 |
| Gimenez Molina A, Barvik I, Müller S, et al. (2018) RNA-based boronate internucleosidic linkages: an entry into reversible templated ligation and loop formation. Organic & Biomolecular Chemistry |