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 63 checked references that resolve
resolves10.1002/ejic.200800323Donor‐Functionalised N‐Heterocyclic Carbene Complexes of Group 9 and 10 Metals in Catalysis: Trends and Directions
resolves10.1002/ejic.200801095Mono‐, Bi‐ and Tridentate N‐Heterocyclic Carbene Ligands for the Preparation of Transition‐Metal‐Based Homogeneous Catalysts
resolves10.1002/anie.200601663Palladium Complexes of N‐Heterocyclic Carbenes as Catalysts for Cross‐Coupling Reactions—A Synthetic Chemist's Perspective
resolves10.1021/jo990554oPalladium−Imidazol-2-ylidene Complexes as Catalysts for Facile and Efficient Suzuki Cross-Coupling Reactions of Aryl Chlorides with Arylboronic Acids
resolves10.1002/adsc.200606009Pyridin‐, Quinolin‐ and Acridinylidene Palladium Carbene Complexes as Highly Efficient C–C Coupling Catalysts
resolves10.1016/j.tet.2005.06.070On the efficiency of two-coordinate palladium(0) N-heterocyclic carbene complexes in amination and Suzuki–Miyaura reactions of aryl chlorides
resolves10.1002/chem.200600283Rapid Room Temperature Buchwald–Hartwig and Suzuki–Miyaura Couplings of Heteroaromatic Compounds Employing Low Catalyst Loadings
resolves10.1021/om8006689<i>N</i>-Heterocyclic Carbenes (NHCs) Containing<i>N</i>-<i>C</i>-Palladacycle Complexes: Synthesis and Reactivity in Aryl Amination Reactions
resolves10.1021/om900677vA Comparative Study on (NHC)Pd(acac)Cl Complexes (NHC = N-heterocyclic carbene): Indications for the Origin of the Different Reactivity of Saturated and Unsaturated NHC in Cross-Coupling Reactions
resolves10.1021/ja0385235Iridium Bis(phosphinite) <i>p</i>-XPCP Pincer Complexes: Highly Active Catalysts for the Transfer Dehydrogenation of Alkanes
resolves10.1021/ja0576684Experimental and Computational Studies on the Mechanism of<i>N</i>-Heterocycle C−H Activation by Rh(I)
resolves10.1016/S0040-4039(99)00217-8Increased ring closing metathesis activity of ruthenium-based olefin metathesis catalysts coordinated with imidazolin-2-ylidene ligands
resolves10.1021/ol990909qSynthesis and Activity of a New Generation of Ruthenium-Based Olefin Metathesis Catalysts Coordinated with 1,3-Dimesityl-4,5-dihydroimidazol-2-ylidene Ligands
resolves10.1021/ja001179gEfficient and Recyclable Monomeric and Dendritic Ru-Based Metathesis Catalysts
resolves10.1021/ja064091xRate Acceleration in Olefin Metathesis through a Fluorine−Ruthenium Interaction
resolves10.1002/chem.2003054371,3‐Dialkyl‐ and 1,3‐Diaryl‐3,4,5,6‐tetrahydropyrimidin‐2‐ylidene Rhodium(<scp>i)</scp> and Palladium(<scp>II</scp>) Complexes: Synthesis, Structure, and Reactivity
resolves10.1021/om800821qIridium and Ruthenium Complexes with Chelating N-Heterocyclic Carbenes: Efficient Catalysts for Transfer Hydrogenation, β-Alkylation of Alcohols, and N-Alkylation of Amines
resolves10.1021/om990776cDonor-Functionalized Heterocyclic Carbene Complexes of Palladium(II): Efficient Catalysts for C−C Coupling Reactions
resolves10.1016/j.ccr.2006.08.003Metal-mediated asymmetric alkylation using chiral N-heterocyclic carbenes derived from chiral amines
resolves10.1039/b503239cUnprecedented use of silver(i) N-heterocyclic carbene complexes for the catalytic preparation of 1,2-bis(boronate) esters
resolves10.1002/ejic.200600209A Cationic (N‐Heterocyclic carbene)silver Complex as Catalyst for Bulk Ring‐Opening Polymerization of <scp>L</scp>‐Lactides
resolves10.1021/ja0782192Highly Site- and Enantioselective Cu-Catalyzed Allylic Alkylation Reactions with Easily Accessible Vinylaluminum Reagents
resolves10.1021/ja040226sSilver(I)−Imidazole Cyclophane <i>gem</i>-Diol Complexes Encapsulated by Electrospun Tecophilic Nanofibers: Formation of Nanosilver Particles and Antimicrobial Activity
resolves10.1021/jm030262mFormation of Water-Soluble Pincer Silver(I)−Carbene Complexes: A Novel Antimicrobial Agent
resolves10.1016/j.jorganchem.2005.07.102Synthesis and crystallographic characterization of multi-donor N-heterocyclic carbene chelating ligands and their silver complexes: Potential use in pharmaceuticals
resolves10.1016/j.biomaterials.2009.03.044The antimicrobial efficacy of sustained release silver–carbene complex-loaded l-tyrosine polyphosphate nanoparticles: Characterization, in vitro and in vivo studies
resolves10.1021/cr800500uThe Medicinal Applications of Imidazolium Carbene−Metal Complexes
resolves10.1021/om9709704Facile Synthesis of Silver(I)−Carbene Complexes. Useful Carbene Transfer Agents
resolves10.1021/ja101490dSelf-Assembly of Molecular Cylinders from Polycarbene Ligands and Ag<sup>I</sup> or Au<sup>I</sup>
resolves10.1039/b007504nN-Functionalised heterocyclic carbene complexes of silver
resolves10.1021/ol048393kA Benzimidazole-Based <i>N</i>-Heterocyclic Carbene Derived from 1,10-Phenanthroline
resolves10.1016/j.tet.2005.03.043A new dimeric bidentated NHC–Pd(II) complex from trans-cyclohexane-1,2-diamine for Suzuki reaction and Heck reaction
resolves10.1021/cm980595lThermally Stable Mesomorphic Palladium(II)−Carbene Complexes
resolves10.1021/cr050004sAg(I) N-Heterocyclic Carbene Complexes: Synthesis, Structure, and Application
resolves10.1016/j.poly.2008.06.006Anellated N-heterocyclic carbenes: 1,3-Dineopentyl-benzimidazol-2-ylidene, structural aspects of C-protonated precursor salts and an AgCl complex
resolves10.1002/hc.20479Palladium <i>N</i>‐heterocyclic‐carbene‐catalyzed ortho‐arylation of benzaldehyde derivatives
resolves10.1016/j.jorganchem.2007.05.019An iodide/anion exchange route to benzimidazolylidene silver complexes from benzimidazolium iodide: Crystal structures of N,N′-dibutylbenzimidazolylidene silver chloride, bromide, cyanide and nitrate
resolves10.1016/S0020-1693(03)00143-9Tetrafluoroborate anion BF bond activation—unusual formation of a nucleophilic heterocyclic carbene:BF3 adduct
resolves10.1021/om0341855Group 11 Metal Complexes of N-Heterocyclic Carbene Ligands: Nature of the MetalCarbene Bond
resolves10.1039/B304474BSilver(
<scp>i</scp>
) complex of a new imino-N-heterocyclic carbene and ligand transfer to palladium(
<scp>ii</scp>
) and rhodium(
<scp>i</scp>
)
The 4 references without a DOI — listed, not checked
no DOI — not checkedClinical and Laboratory Standards Instıtute: Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria That Grow Aerobically; Approved Standard-Seventh Edition, CLSI Document M7-A7, Clinical and Laboratory Standards Instıtute, Wayne, Pennsylvania, USA, 2003.
no DOI — not checkedClinical and Laboratory Standards Instıtute: Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeasts; Approved Standard-Second Edition. NCCLS document M27-A2, NCCLS, 940 West Valley Road, Suite 1400, Wayne, Pennsylvania 19087-1898, USA, 2002, ISBN 1-56238-469-4.
no DOI — not checked10.1016/j.ica.2010.07.034_b0250
no DOI — not checked10.1016/j.ica.2010.07.034_b0330
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