Laurence MIESCH
Chargée de Recherche au CNRS
Year of creation of the group - 2018 (formerly LCOS)
Le Bel Institute, 4th floor South
Elisabeth VACCARO
email : vaccaro@unistra.fr
Phone : +33 (0)3 68 85 16 84
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* works for several groups |
PhD students
1-Developing new methods in organic synthesis: Reactivity of keto-ynamides
2-Phytochemistry
Small molecules that serve as standards for elucidating biosynthetic pathways in plants are being synthesized.
SOPhy offers the possibility of internships (IUT, M1-M2 masters, chemistry schools ...) or to prepare a thesis at the University of Strasbourg. The group is recognized for providing excellent training in synthetic organic chemistry.
SOPhy offers research training based on preparative organic chemistry. The thesis is always considered under its double aspect of original scientific work and period of apprenticeship of a profession.
Lucile Andna and Laurence Miesch
Trapping of N-Acyliminium Ions with Enamides: An Approach to Medium-Sized Diaza-Heterocycles
Org. Lett. 2018, 20, 3430-3433
Clovis Peter, Philippe Geoffroy and Michel Miesch
Intramolecular Morita-Baylis-Hillman reaction as a strategy for the construction of tricyclic sesquiterpene cores
Org. Biomol. Chem.,2018, 16, 1381-1389
Taleb, O., Patte-Mensah, C., Meyer, L., Kemmel, V., Geoffroy, P., Miesch, M., Mensah-Nyagan, A-G.
J. Neuroendocrinol. 2018, DOI: 10.1111/jne.12568
Clovis Peter, Philippe Geoffroy and Michel Miesch
Highly diastereoselective access to polyfunctionalized 1,3-oxazines promoted by Brønsted/Lewis acids
Organic Chemistry Frontiers, 2018, 5, 566
Frédéric Beltran, Indira Fabre, Ilaria Ciofini, and Laurence Miesch
Direct Spirocyclization from Keto-sulfonamides: An Approach to Azaspiro Compounds
Org. Lett., 2017, 19, 5042−5045
C. F. Heinrich, I. Fabre, L. Miesch
Silver Catalyzed 7-exo-dig Cyclization of Silylenolether-ynesulfonamides
Angew. Chem. Int. Ed. 2016, 55, 5170-5174
A small overview of our research group