Institut de Chimie Moléculaire et des Matériaux d'Orsay

Sylvie Robin

Bât. 420CP3A – ICMMO
Université Paris-Saclay
Rue du doyen Georges Poitou
91405 Orsay Cedex

+33 1 69 15 76 30

Sylvie Robin obtained her Ph.D in 1992, from the University of Paris-Sud, in Orsay with Professor F. Huet, working on optically active lactone synthesis. She spent a postdoctoral year at Oxford University with Professor L. M. Harwood, studying cycloadditions with chiral azomethines. Coming back in France, she obtained a teaching position at the Faculty of Pharmacology (Univ. Paris V). In 1995, she joined Dr. G. Rousseau's theme at the University of Paris-Sud, where she studied the reactivity of electrophilic reagents. Since 2009, in Pr. D. J. Aitken’s group, she first worked on the synthesis of conformationally restricted GABA and to the folding behavior of their homo-oligomers and hetero-β,γ-oligomers. Recently she turned her interest to the role of the non-covalent interaction S-H...N in the peptidomimetic oligomers folding. Keywords: amino acids, peptide synthesis, photochemistry, cyclisation, chiral resolution.

Synthesis of enantiopure conformationally restricted GABA via photochemical reaction conditions

Synthesis of sulfured non canonic amino acids

Preparation of homo-oligomers of cis-2,3-cyclobutyl-GABA

Preparation of hetero-oligomers of β,γ-peptides

Publications :

A theoretical and experimental case study of the hydrogen bonding predilection of S-methylcysteine. V. R. Mundlapati, Z. Imani, G. Goldsztejn, E. Gloaguen, V. Brenner, K. Le Barbu-Debus, A. Zehnacker-Rentien, J.-P. Baltaze, S. Robin, M. Mons, D. J. Aitken, Amino Acids, 2021, 53, in press

Conformation control through concurrent N–H⋯S and N–H⋯O=C hydrogen bonding and hyperconjugation effects. Z. Imani, V. R. Mundlapati, G. Goldsztejn, V. Brenner, E. Gloaguen, R. Guillot, J.-P. Baltaze, K. Le Barbu-Debus, S. Robin, A. Zehnacker, M. Mons, D. J. Aitken, Chem. Sci., 2020, 11, 9191-9197

Preparation of cyclobutene acetals and tricyclic oxetanes via photochemical tandem and cascade reactions. J. Buendia, Z. Chang, H. Eijsberg, R. Guillot, A. Frongia, F. Secci, J. Xie, S. Robin, T. Boddaert, D. J. Aitken, Angewandte Chemie International Edition, 2018, 57, 6592-6596

β-Cyclodextrin-Mediated Enantioselective Photochemical Electrocyclization of 1,3-Dihydro-2H-azepin-2-one. A. T. Mansour, J. Buendia, J. Xie, F. Brisset, S. Robin, D. Naoufal, O. Yazbeck, D. J. Aitken, J. Org. Chem., 2017, 82, 9832-9836

Conformational effects through hydrogen bonding in a constrained γ-peptide template: from intra-residue 7-membered rings to a gel-forming sheet structure. H. Awada, C. M. Grison, F. Charnay-Pouget, J.-P. Baltaze, F. Brisset, R. Guillot, S. Robin, A. Hachem, N. Jaber, D. Naoufal, O. Yazbeck, D. J. Aitken, J. Org. Chem., 2017, 82, 4819–4828

An α-Helix-Mimicking 12,13-Helix: Designed α/β/γ-Foldamers as Selective Inhibitors of Protein–Protein Interactions. C. M. Grison, J. A. Miles, S. Robin, A. J. Wilson, D. J. Aitken, Angewandte Chemie International Edition, 2016, 55, 11096-11100

13-Helix folding of a β/γ-peptide manifold designed from a "minimal-constraint" blueprint. C. M. Grison, S. Robin, D. J. Aitken, Chem. Commun., 2016, 52, 7802-7805

The discovery of 9/8-ribbons, β/γ-peptides with curved shapes governed by a combined configuration-conformation code. C. M. Grison, S. Robin, D. J. Aitken, Chem. Commun., 2015, 51, 16233-16236

Pushing the limits of signal resolution to make coupling measurement easier. J. E. H. Pucheta, D. Pitoux, C. M. Grison, S. Robin, D. Merlet, D. J. Aitken, N. Giraud, J. Farjon, Chem Commun, 2015, 51, 7939-7942

Practical Syntheses of Both Enantiomers of the Conformationally Restricted GABA Analogue cis-(2-Aminocyclobutyl)acetic Acid. H. Awada, S. Robin, R. Guillot, O. Yazbeck, D. Naoufal, N. Jaber, A. Hachem, D. J. Aitken, European Journal of Organic Chemistry, 2014, 2014, 7148-7155