about
[{Au(IPr)}2(μ-OH)]X complexes: synthetic, structural and catalytic studies.Iron-catalyzed hydrogenation, hydride transfer, and hydrosilylation: an alternative to precious-metal complexes?Designing NHC-Copper(I) Dipyridylamine Complexes for Blue Light-Emitting Electrochemical Cells.Cytotoxicity of gold(I) N-heterocyclic carbene complexes assessed by using human tumor cell lines.The role of silver additives in gold-mediated C-H functionalisation.A versatile gold synthon for acetylene C-H bond activation.Synthesis and characterization of IPr(Me)-containing silver(I), gold(I) and gold(III) complexes.PtCl2-catalyzed [6+2] cycloaddition of alkynes tethered to cycloheptatriene.Iron(II)-catalysed [2+2+2] cycloaddition for pyridine ring construction.Bifunctional (cyclopentadienone)iron-tricarbonyl complexes: synthesis, computational studies and application in reductive amination.N-heterocyclic carbene gold(I) and copper(I) complexes in C-H bond activation.Role of the Bridging Group in Bis-Pyridyl Ligands: Enhancing Both the Photo- and Electroluminescent Features of Cationic (IPr)CuI Complexes.Antipseudomonal activity enhancement of luminescent iridium(iii) dipyridylamine complexes under visible blue light.Large irradiation doses can improve the fast neutron/gamma discriminating capability of plastic scintillators.Iron-Catalyzed Chemoselective Reduction of α,β-Unsaturated Ketones.Competitive Gold-Promoted Meyer-Schuster and oxy-Cope Rearrangements of 3-Acyloxy-1,5-enynes: Selective Catalysis for the Synthesis of (+)-(S)-γ-Ionone and (−)-(2S,6 R)-cis-γ-IroneGold-mediated synthesis of α-iononeGold-Catalyzed Meyer−Schuster Rearrangement: Application to the Synthesis of ProstaglandinsLuminescent Hyperbranched Polymers: Combining Thiol-Yne Chemistry with Gold-Mediated C−H Bond ActivationPhosphate binding to the [Au(IPr)] moiety: inner vs. outer sphere coordination behaviourA combined mechanistic and computational study of the gold(I)-catalyzed formation of substituted indenesEfficient silver-free gold(I)-catalyzed hydration of alkynes at low catalyst loadingGold(i)-catalyzed synthesis of furans and pyrroles via alkyne hydrationPolymerization of Racemic β-Butyrolactone Using Gold Catalysts: A Simple Access to Biodegradable PolymersSelectivity Switch in the Synthesis of Vinylgold(I) IntermediatesA N-heterocyclic carbene gold hydroxide complex: a golden synthonDevelopment of Versatile and Silver-Free Protocols for Gold(I) CatalysisExpeditious Synthesis of [Au(NHC)(L)]+(NHC = N-Heterocyclic Carbene; L = Phosphine or NHC) Complexes†Ligand influence in the selective gold-mediated synthesis of allenesSynthetic and Structural Studies of [AuCl3(NHC)] ComplexesAlkylation of Ketones Catalyzed by Bifunctional Iron Complexes: From Mechanistic Understanding to ApplicationHighly Active Phosphine-Free Bifunctional Iron Complex for Hydrogenation of Bicarbonate and Reductive AminationRoom-Temperature Chemoselective Reductive Alkylation of Amines Catalyzed by a Well-Defined Iron(II) Complex Using HydrogenRuthenium-catalyzed intramolecular homo-diels-alder reaction of alkyne-tethered norbornadienes. An entry to fused angular triquinanesKnölker's iron complex: an efficient in situ generated catalyst for reductive amination of alkyl aldehydes and aminesIron-catalyzed hydrogenation of esters to alcoholsWhen phosphorus and NHC (N-heterocyclic carbene) meet each otherNHC copper(I) complexes bearing dipyridylamine ligands: synthesis, structural, and photoluminescent studiesCorrection to NHC Copper(I) Complexes Bearing Dipyridylamine Ligands: Synthesis, Structural, and Photoluminescent StudiesIron-Catalyzed α-Alkylation of Ketones with Secondary Alcohols: Access to β-Disubstituted Carbonyl Compounds
P50
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P50
description
researcher ORCID ID = 0000-0003-3402-2518
@en
name
Sylvain Gaillard
@ast
Sylvain Gaillard
@en
Sylvain Gaillard
@es
Sylvain Gaillard
@nl
type
label
Sylvain Gaillard
@ast
Sylvain Gaillard
@en
Sylvain Gaillard
@es
Sylvain Gaillard
@nl
prefLabel
Sylvain Gaillard
@ast
Sylvain Gaillard
@en
Sylvain Gaillard
@es
Sylvain Gaillard
@nl
P69
P1153
34871938200
P21
P31
P496
0000-0003-3402-2518