N
Nicolas Audic
Researcher at Centre national de la recherche scientifique
Publications - 11
Citations - 805
Nicolas Audic is an academic researcher from Centre national de la recherche scientifique. The author has contributed to research in topics: Catalysis & Ionic liquid. The author has an hindex of 7, co-authored 11 publications receiving 767 citations. Previous affiliations of Nicolas Audic include University of Lyon & École Normale Supérieure.
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An ionic liquid-supported ruthenium carbene complex: a robust and recyclable catalyst for ring-closing olefin metathesis in ionic liquids.
TL;DR: The synthesis of an ionic liquid-supported olefin metathesis catalyst derived from Grubb's ruthenium carbene complex, which shows a remarkable stability in BMI.PF6 solvent, and this allowed success in solving the challenging problem of catalyst recycling.
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Synthesis of Benzocyclobutenes by Palladium-Catalyzed C−H Activation of Methyl Groups: Method and Mechanistic Study
Manon Chaumontet,Riccardo Piccardi,Nicolas Audic,Julien Hitce,Jean-Louis Peglion,Eric Clot,Olivier Baudoin +6 more
TL;DR: DFT(B3PW91) calculations on the reaction of 2-bromo-tert-butylbenzene with Pd(P ( t )Bu 3) with different bases showed the critical influence of the coordination mode of the base to induce both an easy C-H activation and to allow for a pathway for 1,4-palladium migration.
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Design and synthesis of imidazolinium salts derived from (L)-valine. Investigation of their potential in chiral molecular recognition
TL;DR: In this article, several imidazolinium salts are synthesized from (L)-valine and a study of the structure relationships is achieved to obtain high diastereomeric interactions with an anionic substrate.
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Olefin metathesis in room temperature ionic liquids using imidazolium-tagged ruthenium complexes
TL;DR: In this article, new recyclable imidazolium-tagged ruthenium catalysts have been developed to perform olefin metathesis in room temperature ionic liquids (RTILs).
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Ring-closing metathesis in biphasic BMI.PF6 ionic liquid/toluene medium: a powerful recyclable and environmentally friendly process.
TL;DR: High levels of recyclability and reusability combined with a high reactivity were obtained with a variety of di- or tri-substituted and/or oxygen-containing dienes, and very low residual ruthenium levels were detected in the products.