Jieping Zhu
EPFL SB ISIC LSPN
BCH 5304 (Batochime UNIL)
Av. F.-A. Forel 2
1015 Lausanne
+41 21 693 97 42
+41 21 693 97 41
Office: BCH 5304
EPFL › SB › ISIC › LSPN
Website: https://lspn.epfl.ch
EPFL SB ISIC LSPN
BCH 5304 (Batochime UNIL)
Av. François-Alphonse Forel 3
1015 Lausanne
+41 21 693 97 41
Office: BCH 5304
EPFL › SB › SB-SCGC › SCGC-ENS
Website: https://www.epfl.ch/schools/sb/scgc/
EPFL SB ISIC LSPN
BCH 5304 (Batochime UNIL)
Av. François-Alphonse Forel 3
1015 Lausanne
+41 21 693 97 41
Office: BCH 5304
EPFL › VPA › VPA-AVP-DLE › AVP-DLE-EDOC › EDCH-ENS
Teaching & PhD
PhD Students
Morgane Elodie Marie Delattre, Paul Jean Gri, Clément Paul Adrien Rols, Yun Hao Shawn Teh
Past EPFL PhD Students
Jean-Baptiste Gualtierotti, Ala Bunescu, Thomas Buyck, Olivier Wagnières, Minh Tu Ha, Dylan Jean Robert Dagoneau, Antonin François Roland Clemenceau, Cyril Piemontesi, Nicolas David Gaeng, Mathias Mamboury, Raphaël Beltran, Balázs Budai, Teerawat Songsichan, Alexandre Julien Florent Leclair, Bastien Delayre, Rémi Julien Sylvain Andres, Dina Boyarskaya, Rémi Lavernhe, Cédric Fung, Takuji Fujii, Vincent Léon Norbert Goëlo, Dan Forster
Past EPFL PhD Students as codirector
Courses
Modern Organic chemistry-Highlights in the field
CH-640
Total synthesis, Natural product, Green chemistry, nantioselective synthesis, Organo-catalysis, Lewis acid,Transition-metal, Drug discovery.
Organic chemistry laboratory Work
CH-230
Purification methods (distillation, crystallization, chromatography), simple organic syntheses: bromination, reduction, acylation, imine, nitration, Grignard, Reformatsky) Acquisition of knowledge on the chemical hazards and how to protect ourself. Knowledge of legal commitments.
Organic functions and reactions I
CH-233
The course will focus on the reactivity of carbonyl compounds: their structure, reactivity and transformations; the reaction of enols/enolates. The understanding of reaction mechanisms, chemo-, regio- and stereo-selectivities will be emphasized.
Synergism between Art of Total Synthesis and High Level Strategic Design (MOM)
CH-622
Retro-synthessis, Total Synthesis, Atom-economy
Total synthesis of natural products
CH-438
Complex polycyclic natural products are chosen to illustrate the evolution of the state-of-the-art of the field, the interplay between strategy and new reactions as well as the importance of implementing multi-bond forming processes in a synthesis.