In this project, we intend to develop bio-inspired FDHs Mo/W-peptidic systems with the final goal of obtaining efficient molecular catalysts for CO2 reduction. Different peptidic scaffolds that will contain non-natural dithiolene-like amino acids to coordinate Mo and/or W will be designed and...
The global dependence on fossil fuels as energy carriers and as raw materials for industrial products presents a huge challenge for the coming decades. Global demand for energy is increasing steadily and fossil fuels made up more than 80% of global energy consumption in 2017. Alternatives such...
Bioactive Lignans: from natural products to drugs, via stereoselective control of free radical coupling: Study of stereoselective coupling mechanisms of radicals by auxiliary proteins for the development of biocatalysts:
We look for a PhD student (M/F) in organic chemistry and enantioselective catalysis for a 36-month period starting in September or October 2020, with funding provided by the ANR (Agence Nationale de la Recherche = French National Research Agency) project Bond-X-Bond (ANR JCJC 2019).
Our research group recently developed conversion of chirality strategies for the control of axial chirality.2 The goal of this PhD project is to design and develop enantioselective synthetic strategies towards [n]heterohelicenes relying on the combination of organocatalysis with conversion of...
Une bourse de thèse (36 mois) est ouverte à candidature à l’Institut des Sciences Moléculaire de Marseille (iSm2-UMR CNRS 7313), dans l’équipe STeRéO, sous la direction des Drs Olivier Chuzel et Jean-Luc Parrain.
A CNRS funded PhD position in the field of artificial photo-synthesis is available at Ism2 (BiosCiences team) starting October 1st 2020.
Theme: Modelling of properties of 4th row metals
Project:
In catalysis today, chemists aim to reduce the use of metals of the second and third transition series, in order to develop the chemistry of the more available and cheaper elements of the...
Des chercheurs de l’Institut des sciences moléculaires de Marseille (CNRS/Aix-Marseille Université) ont mis au point une méthode très efficace permettant de sélectionner la molécule désirée parmi les deux formes sous lesquelles se présente une molécule chirale, grâce à deux réactions sélectives successives. Ces travaux, publiés dans Angewandte Chemie International Edition, ont des applications pour de nombreux produits d’intérêt biologique dont les médicaments.
Veuillez cliquer ici pour lire l'article sur le site Web du CNRS
