Michel Miesch
Affiliations: | Chimie | Université de Strasbourg/CNRS |
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Sign in to add trainee| Christian Schäfer | grad student | 2009-2013 | Université de Strasbourg/CNRS |
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| Shiina I, Miesch M, Peter C, et al. (2019) Diastereo–/Enantioselective Diels–Alder Synthesis of 14β-Hydroxysteroid Scaffolds: A Combined Experimental and DFT Study Heterocycles. 99: 1251 |
| Peter C, Geoffroy P, Miesch M. (2018) Intramolecular Morita-Baylis-Hillman reaction as a strategy for the construction of tricyclic sesquiterpene cores. Organic & Biomolecular Chemistry |
| Peter C, Geoffroy P, Miesch M. (2018) Highly diastereoselective access to polyfunctionalized 1,3-oxazines promoted by Brønsted/Lewis acids Organic Chemistry Frontiers. 5: 566-570 |
| Peter C, Ressault B, Geoffroy P, et al. (2016) Concise Approach to (ent)-14 β-Hydroxysteroids through Highly Diastereo-/Enantioselective Diels-Alder Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 10808-12 |
| Heinrich CF, Peter C, Miesch L, et al. (2016) Diastereo- and Enantioselective Synthesis of Polyfunctionalized Diquinanes, Hydrindanes, and Decalins Bearing a Hydroxyl Group at the Ring Junction Synthesis (Germany). 48: 1607-1615 |
| Boachon B, Junker RR, Miesch L, et al. (2015) CYP76C1 (Cytochrome P450)-Mediated Linalool Metabolism and the Formation of Volatile and Soluble Linalool Oxides in Arabidopsis Flowers: A Strategy for Defense against Floral Antagonists. The Plant Cell. 27: 2972-90 |
| Boehringer R, Geoffroy P, Miesch M. (2015) Base catalyzed synthesis of bicyclo[3.2.1]octane scaffolds. Organic & Biomolecular Chemistry. 13: 6940-3 |
| Heinrich CF, Miesch M, Miesch L. (2015) In situ intramolecular catalytic 1,2-addition of allenoates to cyclic ketones towards polycyclic allenoates. Organic & Biomolecular Chemistry. 13: 2153-6 |
| Geoffroy P, Bl, Ressault i, et al. (2015) Synthesis of Hoodigogenin A, the Aglycone of Hoodigosides Extractedfrom Hoodia gordonii Journal of Steroids & Hormonal Science. 6: 1-5 |
| Heinrich CF, Widemann E, Sanz J, et al. (2015) A route for the total synthesis of enantiomerically enriched jasmonates 12-COOH-JA and 12-COOH-JA-Ile European Journal of Organic Chemistry. 2015: 1130-1136 |