Every reference with a DOI in the deposited reference list resolved to a known
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withdrawal, or removal notice.
The 110 checked references that resolve
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resolves10.1016/j.jinorgbio.2007.09.003In vitro antitumour and hepatotoxicity profiles of Au(I) and Ag(I) bidentate pyridyl phosphine complexes and relationships to cellular uptake
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resolves10.1039/b008038lA Pd complex of a tridentate pincer CNC bis-carbene ligand as a robust homogenous Heck catalyst
resolves10.1039/b902238bBeyond catalysis: N-heterocyclic carbene complexes as components for medicinal, luminescent, and functional materials applications
resolves10.1021/jm0708679Synthesis, Stability, and Antimicrobial Studies of Electronically Tuned Silver Acetate <i>N</i>-Heterocyclic Carbenes
resolves10.1002/ejic.200900889Synthesis, Cytotoxicity and Antibacterial Studies of <i>p</i>‐Methoxybenzyl‐Substituted and Benzyl‐Substituted N‐Heterocyclic Carbene–Silver Complexes
resolves10.1002/zaac.201000395Synthesis, Cytotoxicity and Antibacterial Studies of Novel Symmetrically and Non‐Symmetrically <i>p</i>‐Nitrobenzyl‐Substituted N‐Heterocyclic Carbene–Silver(I) Acetate Complexes
resolves10.1039/C0MT00034ENovel benzyl-substituted N-heterocyclic carbene–silver acetate complexes: synthesis, cytotoxicity and antibacterial studies
resolves10.1002/aoc.1702Synthesis, cytotoxicity and antibacterial studies of symmetrically and non‐symmetrically benzyl‐ or <i>p</i>‐cyanobenzyl‐substituted <i>N</i>‐Heterocyclic carbene–silver complexes
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N
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resolves10.1002/chem.201100321Cytotoxicity of Gold(I) N‐Heterocyclic Carbene Complexes Assessed by Using Human Tumor Cell Lines
resolves10.1039/c0cc00018cA N-heterocyclic carbene gold hydroxide complex: a golden synthon
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resolves10.1021/jm100801eBenzimidazol-2-ylidene Gold(I) Complexes Are Thioredoxin Reductase Inhibitors with Multiple Antitumor Properties
resolves10.1021/jm800101wGold(I)-Mediated Inhibition of Protein Tyrosine Phosphatases: A Detailed in Vitro and Cellular Study
resolves10.1039/c001216eCyclometalated gold(iii) complexes with N-heterocyclic carbene ligands as topoisomerase I poisons
resolves10.1002/chem.200600117Anticancer Cyclometalated [Au<sup>III</sup><sub><i>m</i></sub>(C<sup>∧</sup>N<sup>∧</sup>C)<sub><i>m</i></sub>L]<sup><i>n</i>+</sup> Compounds: Synthesis and Cytotoxic Properties
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resolves10.1021/jm00281a001Oral gold. Antiarthritic properties of alkylphosphinegold coordination complexes
resolves10.1016/j.jorganchem.2005.07.013Synthesis and structural characterisation of linear Au(I) N-heterocyclic carbene complexes: New analogues of the Au(I) phosphine drug Auranofin
resolves10.1039/C0MD00181CThioredoxin reductase, an emerging target for anticancer metallodrugs. Enzyme inhibition by cytotoxic gold(iii) compounds studied with combined mass spectrometry and biochemical assays
resolves10.1002/anie.200502756Undressing of Phosphine Gold(
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resolves10.1039/b602560aCationic, linear Au(i) N-heterocyclic carbene complexes: synthesis, structure and anti-mitochondrial activity
resolves10.1002/anie.200601526Luminescence Studies of the Intracellular Distribution of a Dinuclear Gold(I) N‐Heterocyclic Carbene Complex
resolves10.1016/j.jinorgbio.2004.05.011Mitochondrial permeability transition induced by dinuclear gold(I)–carbene complexes: potential new antimitochondrial antitumour agents
resolves10.1021/jm201220nComparative in Vitro Evaluation of N-Heterocyclic Carbene Gold(I) Complexes of the Benzimidazolylidene Type
resolves10.1002/cmdc.201200055Anticancer Activity of Silver–<i>N</i>‐Heterocyclic Carbene Complexes: Caspase‐Independent Induction of Apoptosis via Mitochondrial Apoptosis‐Inducing Factor (AIF)
resolves10.1039/b906140aSynthesis, structural characterisation and anti-proliferative activity of NHC gold amino acid and peptide conjugates
resolves10.1039/c2sc01127aA spontaneous gold(i)-azide alkyne cycloaddition reaction yields gold-peptide bioconjugates which overcome cisplatin resistance in a p53-mutant cancer cell line
resolves10.1021/jm300428vGold(I) Carbene Complexes Causing Thioredoxin <b>1</b> and Thioredoxin <b>2</b> Oxidation as Potential Anticancer Agents
resolves10.1021/jm101096xPreparation and Characterization of Amino-Linked Heterocyclic Carbene Palladium, Gold, and Silver Complexes and Their Use as Anticancer Agents That Act by Triggering Apoptotic Cell Death
resolves10.1016/j.jinorgbio.2006.12.008Synthesis and mass spectroscopy kinetics of a novel ternary copper(II) complex with cytotoxic activity against cancer cells
resolves10.1021/ic980044xPreparation of the New Bis(phenanthroline) Ligand “Clip-Phen” and Evaluation of the Nuclease Activity of the Corresponding Copper Complex
resolves10.1021/jm701146cIn Vitro Antitumor Activity of the Water Soluble Copper(I) Complexes Bearing the Tris(hydroxymethyl)phosphine Ligand
resolves10.1039/b719904jLarge-bite bis(phosphite) ligand containing mesocyclic thioether moieties: synthesis, reactivity, group 11 (CuI, AuI) metal complexes and anticancer activity studies on a human cervical cancer (HeLa) cell line
resolves10.1002/chem.200600961(NHC)Copper(<scp>I</scp>)‐Catalyzed [3+2] Cycloaddition of Azides and Mono‐ or Disubstituted Alkynes
resolves10.1002/chem.200801992Toxicity of Copper(I)–NHC Complexes Against Human Tumor Cells: Induction of Cell Cycle Arrest, Apoptosis, and DNA Cleavage
resolves10.1002/cbic.200400243Cytostatic Activity of 1,10‐Phenanthroline Derivatives Generated by the Clip‐Phen Strategy
resolves10.1021/jm901693mN-Heterocyclic Carbene-Amine Pt(II) Complexes, a New Chemical Space for the Development of Platinum-Based Anticancer Drugs
resolves10.1016/j.jorganchem.2005.08.020Synthetic and structural studies of NHC–Pt(dvtms) complexes and their application as alkene hydrosilylation catalysts (NHC = N-heterocyclic carbene, dvtms = divinyltetramethylsiloxane)
resolves10.1039/c0sc00593bLuminescent cyclometalated platinum(ii) complexes containing N-heterocyclic carbene ligands with potent in vitro and in vivo anti-cancer properties accumulate in cytoplasmic structures of cancer cells
resolves10.1039/c1cc11391gDirect functionalisation of group 10 N-heterocyclic carbene complexes for diversity enhancement
resolves10.1039/B912608BMetal chelating systems synthesized using the copper(i) catalyzed azide-alkynecycloaddition
resolves10.1016/j.tetlet.2005.01.033A palladium Chugaev carbene complex as a modular, air-stable catalyst for Suzuki–Miyaura cross-coupling reactions
resolves10.1002/ejic.200800366The Synthesis of Ruthenium and Rhodium Complexes with Functionalized N‐Heterocyclic Carbenes and Their Use in Solid Phase Peptide Synthesis
resolves10.1089/zeb.2009.0601Biomedical Properties of a Series of Ruthenium-N-Heterocyclic Carbene Complexes Based on Oxidant Activity
<i>In Vitro</i>
and Assessment
<i>In Vivo</i>
of Biosafety in Zebrafish Embryos
resolves10.1155/2015/859730Anticancer Activities of Mononuclear Ruthenium(II) Coordination Complexes
resolves10.1039/c0dt01816cRuthenium anticancer compounds: myths and realities of the emerging metal-based drugs
resolves10.1021/bc200565vCholesterol-Based Nucleolipid-Ruthenium Complex Stabilized by Lipid Aggregates for Antineoplastic Therapy
resolves10.1002/ejic.201300820Synthesis, Cellular Uptake and Biological Activity Against Pathogenic Microorganisms and Cancer Cells of Rhodium and Iridium N‐Heterocyclic Carbene Complexes Bearing Charged Substituents
resolves10.1021/om500140gTemplate-Directed Synthesis of Palladium(II) Sulfonate-NHC Complexes and Catalytic Studies in Aqueous Mizoroki–Heck Reactions
resolves10.1007/BF02376078Triple ion-type imidazolium salts: A new class of single-ion conductive matrix
resolves10.1021/om500753vWater-Soluble Mono- and Dimethyl N-Heterocyclic Carbene Platinum(II) Complexes: Synthesis and Reactivity
resolves10.1021/cr800403rHydrophilic Ligands and Their Application in Aqueous-Phase Metal-Catalyzed Reactions
resolves10.1016/j.jorganchem.2016.01.018Novel multicharged silver(I)–NHC complexes derived from zwitterionic 1,3-symmetrically and 1,3-unsymmetrically substituted imidazoles and benzimidazoles: Synthesis and cytotoxic properties
resolves10.1016/j.jinorgbio.2013.09.011Synthesis and in vitro antitumor activity of water soluble sulfonate- and ester-functionalized silver(I) N-heterocyclic carbene complexes
resolves10.1021/om9010966Syntheses, Structures, and Catalytic Activities of Hemilabile Thioether-Functionalized NHC Complexes
resolves10.1016/j.ica.2009.02.035Synthesis, structural characterization and catalytic activity of a palladium(II) complex bearing a new ditopic thiophene-N-heterocyclic carbene ligand
resolves10.1016/j.tetasy.2010.06.041Axially chiral C2-symmetric N-heterocyclic carbene (NHC) palladium complexes-catalyzed asymmetric arylation of aldehydes with arylboronic acids
resolves10.1002/hlca.201100107Novel Benzyl‐ or 4‐Cyanobenzyl‐Substituted N‐Heterocyclic (Bromo)(carbene)silver(I) and (Carbene)(chloro)gold(I) Complexes: Synthesis and Preliminary Cytotoxicity Studies
resolves10.1039/c1cc15908aSilver metallation of hen egg white lysozyme: X-ray crystal structure and NMR studies
resolves10.1016/j.ica.2012.10.029Synthesis and biological evaluation of N-heterocyclic carbene–silver(I) acetate complexes derived from 4,5-ditolyl-imidazole
resolves10.1080/00958972.2014.911291Synthesis, characterization, and transfer hydrogenation of Ru(II)-<i>N</i>-heterocyclic carbene complexes
resolves10.3390/ijms18091856PSFM-DBT: Identifying DNA-Binding Proteins by Combing Position Specific Frequency Matrix and Distance-Bigram Transformation
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no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib14c
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no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib19e
no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib20a
no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib20d
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no DOI — not checkedP. Mailliet, A. Marinetti and M. Skander, WO/2009/118475, 2009.
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no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib36
no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib37
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