Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 44 checked references that resolve
resolves10.1073/pnas.0307928100Toward efficient asymmetric hydrogenation: Architectural and functional engineering of chiral molecular catalysts
resolves10.1038/nchem.539Organocatalytic cascade reactions as a new tool in total synthesis
resolves10.1021/op049950lA Practical Building Block for the Synthesis of Discodermolide
resolves10.1021/cr0509556A Green Chemistry Approach to Asymmetric Catalysis: Solvent-Free and Highly Concentrated Reactions
resolves10.1039/c004970kIn water, on water, and by water: mimicking nature's aldolases with organocatalysis and water
resolves10.1002/chem.200700363Highly Diastereo‐ and Enantioselective Direct Aldol Reactions of Aldehydes and Ketones Catalyzed by Siloxyproline in the Presence of Water
resolves10.1002/anie.200700909Diphenylprolinol Silyl Ether as a Catalyst in an Enantioselective, Catalytic, Tandem Michael/Henry Reaction for the Control of Four Stereocenters
resolves10.1021/ol061964jPolystyrene-Supported Hydroxyproline: An Insoluble, Recyclable Organocatalyst for the Asymmetric Aldol Reaction in Water
resolves10.1016/j.catcom.2007.12.015Polystyrene-supported proline as recyclable catalyst in the Baylis–Hillman reaction of arylaldehydes and methyl or ethyl vinyl ketone
resolves10.1002/chir.20603Asymmetric aldol reactions catalyzed by efficient and recyclable silica‐supported proline‐based peptides
resolves10.1002/adsc.200606059Ionic‐Liquid‐Supported Organocatalyst: Efficient and Recyclable Ionic‐Liquid‐Anchored Proline for Asymmetric Aldol Reaction
resolves10.1002/adsc.200505227Supported Ionic Liquids. New Recyclable Materials for the <scp>L</scp>‐Proline‐Catalyzed Aldol Reaction
resolves10.1039/b709471jNew ionic liquid-modified silica gels as recyclable materials for l-proline- or H–Pro–Pro–Asp–NH2-catalyzed aldol reaction
resolves10.1039/b711298jMagnetic nanoparticle-supported proline as a recyclable and recoverable ligand for the CuI catalyzed arylation of nitrogen nucleophiles
resolves10.1021/ol061418qHighly Efficient and Reusable Dendritic Catalysts Derived from<i>N</i>-Prolylsulfonamide for the Asymmetric Direct Aldol Reaction in Water
resolves10.1039/b703016aPolymer-supported proline-decorated dendrons: dendritic effect in asymmetric aldol reaction
resolves10.1039/b607342eArtificial aldolases from peptide dendrimer combinatorial libraries
resolves10.1039/b903921jFunctionalized nanoparticles as catalysts for enantioselective processes
resolves10.1021/la702886qEnvironmentally Friendly Synthesis of Highly Monodisperse Biocompatible Gold Nanoparticles with Urchin-like Shape
resolves10.1002/cbic.200800843Shuttling Gold Nanoparticles into Tumoral Cells with an Amphipathic Proline‐Rich Peptide
resolves10.1021/ja960198gMonolayers in Three Dimensions: Synthesis and Electrochemistry of ω-Functionalized Alkanethiolate-Stabilized Gold Cluster Compounds
resolves10.1021/la981598fDynamics of Place-Exchange Reactions on Monolayer-Protected Gold Cluster Molecules
resolves10.1039/C39940000801Synthesis of thiol-derivatised gold nanoparticles in a two-phase Liquid–Liquid system
resolves10.1002/aoc.1382Transition‐metal nanoparticles: synthesis, stability and the leaching issue
resolves10.1021/cs200495sChemical Synthesis of Complex Molecules Using Nanoparticle Catalysis
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