Accueil › Annuaire des chercheurs › Mathieu Sauthier
Mathieu Sauthier
Affiliation : Centre National de la Recherche Scientifique · École Nationale Supérieure de Chimie de Lille · Université de Lille · Unité de Catalyse et Chimie du Solide · Université d'Artois · Centrale Lille Institut
- 31Publications (affiliation française)
- 214Publications au total
- 2046Citations
- 24Indice h
Profil de recherche
Mathieu Sauthier compte 31 publications référencées (2016–2025). Ses travaux paraissent principalement dans « Inorganica Chimica Acta », « Journal of Molecular Structure » et « RSC Advances ». Son article le plus cité, « Nickel(0)‐Catalyzed N‐Allylation of Amides and p‐Toluenesulfonamide with Allylic Alcohols under Neat and Neutral Conditions » (2016), a été cité 38 fois. 15 de ces publications datent des trois dernières années d’activité. Ses travaux sont cosignés avec au moins 12 chercheurs, notamment dans des établissements de Maroc.
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Créer mon profil gratuit Ajouter mes publicationsDomaines de recherche
- Catalytic Cross-Coupling Reactions
- Organometallic Complex Synthesis and Catalysis
- Catalytic Alkyne Reactions
- Asymmetric Synthesis and Catalysis
- Crystal structures of chemical compounds
Publications (31)
- Biological impact of Pd(II) complexes: Synthesis, crystal structure, Hirshfeld surface analysis, NCI-RDG, molecular docking, molecular dynamic simulations
- Synthesis, characterization and biological screening of N-heterocyclic carbene Ag(I) catalysts for aldehyde–amine–alkyne coupling reaction
- Novel Nonsymmetrically benzimidazolium salts and their silver(I)-N-heterocyclic carbene complexes: Synthesis, crystal structure, DFTstudies and anticancer activities
- Novel nonsymmetrically benzimidazolium salts and their silver(I)-N-heterocyclic carbene complexes: Synthesis, DFT study and Anticancer activities
- Pd–PEPPSI-type expanded ring N-heterocyclic carbene complexes: synthesis, characterization, and catalytic activity in Suzuki–Miyaura cross coupling
- Al(OiPr)3 as an effective catalyst for the enhancement of Meerwein−Ponndorf−Verley (MPV) reductions of Morita-Baylis-Hillman (MBH) cyclic alcohols
- An efficient palladium catalyzed mizoroki-heck cross-coupling in water: synthesis, characterization and catalytic activities
- Complexation of Terpenes for the Production of New Antimicrobial and Antibiofilm Molecules and Their Encapsulation in Order to Improve Their Activities
- Synthesis of palladium complexes containing benzimidazole core and their catalytic activities in direct C H functionalization of five-membered heterocyclic bioactive motifs
- Plausible PEPPSI catalysts for direct C–H functionalization of five-membered heterocyclic bioactive motifs: synthesis, spectral, X-ray crystallographic characterizations and catalytic activity
- Copper-Catalyzed Asymmetric Hydroboration Reaction of Novel Methylene Isoindolinone Compounds through Microwave Irradiation and Their Antileishmanial and Antitoxoplasma Activities
- Efficient and Sustainable One‐pot Synthesis of α‐Carbonyl Homoallylic Alcohols from Benzaldehyde and Allylic Alcohols Using both NHC and Nickel Catalysts
- Palladium( ii )/N-heterocyclic carbene (NHC) catalyzed direct C–H arylation of heteroarenes with different aryl bromides and chlorides
- Sustainable and selective Ni-catalyzed allylation of 2-oxindoles and 2-coumaranones in batch and flow chemistry
- Nickel-catalyzed allylation reactions with allylic alcohol
- Ruthenium(II) complexes bearing benzimidazole-based N-heterocyclic carbene (NHC) ligands as potential antimicrobial, antioxidant, enzyme inhibition, and antiproliferative agents
- Synthesis and crystal structures of palladium complexes based on α -amino-oximes derived from ( R )-limonene and their application in allylic alkylation of 1,3-dioxo compounds
- The Selective Nickel‐Catalyzed N‐Allylation of C3‐Unprotected Indoles under Mild and Clean Conditions
- Copper-Catalyzed Hydroboration of Enamides with Bis(pinacolato)diboron: Promising Agents with Antimicrobial Activities
- Substituted N-heterocyclic carbene PEPPSI-type palladium complexes with different N-coordinated ligands: Involvement in the direct C H bond activation of heteroarenes derivatives with aryl bromide and their antimicrobial, anti-inflammatory and antioxidant activities
- Synthesis, characterization and in vitro bioactivity studies of isoindolin‐1‐3‐phosophonate compounds
- Efficient and Clean Nickel Catalyzed α‐Allylation Reaction of Nitriles
- Synthesis and Characterization of 3-Methylene Isoindolinones by Two Synthetic Routes
- Synthesis and crystal structure of a new chiral α-aminooxime nickel(II) complex
- An Efficient, Three-Component Synthesis of Isoindolin-1-One-3-Phosphonates Under Mild and Solvent-Free Conditions and Their Biological Activities
- In Vitro Bioactivities of Isoindolin-1-3-Phosophonate Compounds
- The salt-free nickel-catalysed α-allylation reaction of ketones with allyl alcohol and diallylether
- An Efficient Synthesis of Phthalimides and Their Biological Activities
- Efficient in situ N-heterocyclic carbene palladium( ii ) generated from Pd(OAc) 2 catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities
- Correction: Efficient in situ N-heterocyclic carbene palladium( ii ) generated from Pd(OAc) 2 catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities
- Nickel(0)‐Catalyzed N‐Allylation of Amides and p‐Toluenesulfonamide with Allylic Alcohols under Neat and Neutral Conditions
Revues de publication
- Inorganica Chimica Acta × 3
- Journal of Molecular Structure × 3
- RSC Advances × 3
- European Journal of Organic Chemistry × 2
- Polycyclic aromatic compounds × 2
- Research Square × 2
Publications par année
- 20252
- 20245
- 20238
- 20224
- 20217
- 20202
- 20182
- 20161
Collaborations
Établissements partenaires : Unité Matériaux et Transformations · Abdelmalek Essaâdi University · Institut Catholique d'Arts et Métiers · Cadi Ayyad University · Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement
Pays des co-auteurs : Maroc
Co-auteurs
- Isabelle Suisse
- Bouchaib Mouhsine
- Éric Deniau
- Clément Dumont
- Anthony Saint Pol
- Aurélien Béthegnies
- Yasmina Homrani
- Pauline Loxq
- Maël Penhoat
- Frédéric Capet
- Yousra El Fannassi
- Eric Deniou
Données bibliographiques issues d’OpenAlex (base ouverte).
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