Synthesis of biorelevant scaffolds/molecules

Keywords

biologically active molecules, 1,2-amino-alcohols, 1,3-diols, hydrogenation, asymmetric transfer hydrogenation, enantioselectivity, dynamic kinetic resolution

Members

• Virginie Vidal| 📧
• Phannarath Phansavath| 📧

Selected Publications:

1. P.-G. Echeverria, A. Pons, S. Prévost, C. Férard, J. Cornil, A. Guérinot,J. Cossy, P. Phansavath, V. Ratovelomanana-Vidal, Progress toward the total synthesis of mirabalin isomers, Arkivoc 2019, iv, 44–68. (Special issue: commemorative issue dedicated to Prof S. Hanessian, invitation Prof N. Moitessier)
2. J. Cornil, P.-G. Echeverria, S. Reymond, P. Phansavath, V. Ratovelomanana-Vidal, A. Guérinot, J. Cossy, Synthetic studies toward the C14–C29 fragment of mirabalin, Org. Lett. 2016, 18, 4534–4537.
3. M. Perez, P.-G. Echeverria, E. Martinez-Arripe, M. Ez Zoubir, R. Touati, Z. Zhang, J.-P. Genêt, P. Phansavath, T. Ayad, V. Ratovelomanana-Vidal, An Efficient Stereoselective Total Synthesis of All Stereoisomers of the Antibiotic Thiamphenicol Through Ruthenium-Catalyzed Asymmetric Reduction via Dynamic Kinetic Resolution, Eur. J. Org. Chem. 2015, 5949−5958. (Front cover)
4. G. Pomey, P. Phansavath, Total Synthesis of Laingolide A Diastereomers, Synthesis 2015, 47, 1016−1023.
5. P.-G. Echeverria, S. Prévost, J. Cornil, C. Férard, S. Reymond, A. Guérinot, J. Cossy, V. Ratovelomanana-Vidal, P. Phansavath, Synthetic Strategy toward the C44−C65 Fragment of Mirabalin, Org. Lett. 2014, 16, 2390−2393.