O. Poupardin

Design, Synthesis, and Evaluation of a Novel Series of Indole Sulfonamide Peroxisome Proliferator Activated Receptor (PPAR) α/γ/δ Triple Activators: Discovery of Lanifibranor, a New Antifibrotic Clinical Candidate.

J. Binet, J. Junien, Stéphanie Ferry, 2018, Journal of medicinal chemistry.

Diastereoselective syntheses of α-amino-β-hydroxyesters precursors of the ribosyl-diazepanone core of the liposidomycins

C. Greck, B. Drouillat, Y. Bourdreux, 2003 .

Efficient asymmetric synthesis of a functionalized Δ2-pyrazoline

C. Greck, J. Genêt, O. Poupardin, 2000 .

First approach to the cycloisodityrosine unit of RA-IV

C. Greck, J. Genêt, F. Ferreira, 2001 .

Rapid Asymmetric Synthesis of Highly Functionalized C5 Chiral Synthons. Practical Preparation of trans-3-Hydroxy-D-Proline

C. Greck, J. Genêt, O. Poupardin, 1998 .

Discovery of novel quinoline sulphonamide derivatives as potent, selective and orally active RORγ inverse agonists.

S. Gauld, K. Cusack, M. Kort, 2019, Bioorganic & medicinal chemistry letters.