Jieping Zhu

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Full Professor

jieping.zhu@epfl.ch +41 21 693 97 41

EPFL SB ISIC LSPN
BCH 5304 (Batochime UNIL)
Av. F.-A. Forel 2
CH-1015 Lausanne

+41 21 693 97 41
+41 21 693 97 42
Office: BCH 5304
EPFL > SB > ISIC > LSPN

Web site: Web site: https://lspn.epfl.ch

EPFL SB SCGC-GE
BCH 5304 (Batochime UNIL)
Av. F.-A. Forel 2
CH-1015 Lausanne

+41 21 693 97 41
Office: BCH 5304
EPFL > SB > SB-SCGC > SCGC-ENS

EPFL AVP-PGE EDCH-ENS
BCH 3313 (Batochime UNIL)
Av. F.-A. Forel 2
CH-1015 Lausanne

+41 21 693 97 41
Office: BCH 5304
EPFL > VPA > VPA-AVP-PGE > AVP-PGE-EDOC > EDCH-ENS

EPFL SB SCGC-GE
BCH 3311 (Batochime UNIL)
Av. F.-A. Forel 2
CH-1015 Lausanne

+41 21 693 97 41
Office: BCH 3303
EPFL > SB > SB-SCGC > SCGC-GE

EPFL AVP-E CDS
BP 1133 (Bâtiment BP)
Station 16
CH-1015 Lausanne

+41 21 693 97 41
Office: BP 1133
EPFL > VPA > VPA-AVP-E > AVP-E > AVP-E-CDS

Web site: Web site: https://dms.epfl.ch/DOCS/E/CDS

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Administrative data

Teaching & PhD

Teaching

Chemistry and Chemical Engineering

PhD Programs

Doctoral Program in Chemistry and Chemical Engineering

PhD Students

Andres Rémi Julien Sylvain, Boyarskaya Dina, Forster Dan, Fujii Takuji, Fung Cédric, Goëlo Vincent Léon Norbert, Lavernhe Rémi Hugo,

Past EPFL PhD Students

Beltran Raphaël , Budai Balázs , Bunescu Ala , Buyck Thomas Bertrand Pascal Marie , Clemenceau Antonin François Roland , Dagoneau Dylan Jean Robert , Delayre Bastien , Gaeng Nicolas David , Gualtierotti Jean-Baptiste , Ha Minh Tu , Leclair Alexandre Julien Florent , Mamboury Mathias , Piemontesi Cyril , Reinmüller Viktoria , Songsichan Teerawat , Wagnières Olivier ,

Courses

Organic chemistry laboratory Work

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

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.

Total synthesis of natural products

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.

Perspectives in Modern Organic Chemistry (OCS) 1

Total synthesis, Natural product, Green chemistry, Enantioselective synthesis, Organo-catalysis, Lewis acid, Transition-metal, Drug discovery

Perspectives in Modern Organic Chemistry (OCS) 2