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 52 checked references that resolve
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resolves10.1002/adsc.201300841An Efficient Palladium N‐Heterocyclic Carbene Catalyst Allowing the Suzuki–Miyaura Cross‐Coupling of Aryl Chlorides and Arylboronic Acids at Room Temperature in Aqueous Solution
resolves10.1080/00958972.2013.786053Synthesis and characterization of 1-phenyl-3-alkylbenzimidazol-2-ylidene salts and their catalytic activities in the Heck and Suzuki cross-coupling reactions
resolves10.1016/j.tet.2005.06.060Palladium–benzimidazolium salt catalyst systems for Suzuki coupling: development of a practical and highly active palladium catalyst system for coupling of aromatic halides with arylboronic acids
resolves10.1016/j.jorganchem.2015.05.0472-(diphenylphosphino)pyridine platinum (I) and palladium (I) complex as an efficient binuclear catalyst for Suzuki-Miyaura coupling reaction in water under mild reaction conditions
resolves10.1002/ejoc.201200355An Efficient Class of P,N‐Type “PhMezole‐phos” Ligands: Applications in Palladium‐Catalyzed Suzuki Coupling of Aryl Chlorides
resolves10.1021/om3011992Electron-Rich Trialkyl-Type Dihydro-KITPHOS Monophosphines: Efficient Ligands for Palladium-Catalyzed Suzuki–Miyaura Cross-Coupling. Comparison with Their Biaryl-Like KITPHOS Monophosphine Counterparts
resolves10.1002/chem.200902842Rational Exploration of N‐Heterocyclic Carbene (NHC) Palladacycle Diversity: A Highly Active and Versatile Precatalyst for Suzuki–Miyaura Coupling Reactions of Deactivated Aryl and Alkyl Substrates
resolves10.1080/00958972.2013.819092Palladium catalyzed Mizoroki–Heck and Suzuki–Miyaura reactions using naphthalenomethyl-substituted imidazolidin-2-ylidene ligands in aqueous media
resolves10.1002/anie.199523711Metal Complexes of N‐Heterocyclic Carbenes—A New Structural Principle for Catalysts in Homogeneous Catalysis
resolves10.1002/ejic.200500030Stabilization of Organometallic Species Achieved by the Use of N‐Heterocyclic Carbene (NHC) Ligands
resolves10.1021/om020178pSuzuki−Miyaura Cross-Coupling Reactions Mediated by Palladium/Imidazolium Salt Systems
resolves10.1016/j.ccr.2006.10.004Stereoelectronic parameters associated with N-heterocyclic carbene (NHC) ligands: A quest for understanding
resolves10.1080/00958972.2017.1287906Ring-expanded iridium and rhodium<i>N</i>-heterocyclic carbene complexes: a comparative DFT study of heterocycle ring size and metal center diversity
resolves10.1039/C7NJ00488ESynthesis and catalytic applications of palladium N-heterocyclic carbene complexes as efficient pre-catalysts for Suzuki–Miyaura and Sonogashira coupling reactions
resolves10.1080/00958972.2018.1430791N-Heterocyclic carbene-Pd(II)-PPh
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resolves10.1016/S0022-328X(00)00722-1Synthesis, structure and catalytic application of palladium(II) complexes bearing N-heterocyclic carbenes and phosphines
resolves10.1039/B715412GN-Heterocyclic carbeneligands bearing hydrophilic and/or hydrophobic chains: Rh(
<scp>i</scp>
) and Pd(
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) complexes and their catalytic activity
resolves10.1021/ol026745mWell-Defined, Air-Stable (NHC)Pd(Allyl)Cl (NHC = N-Heterocyclic Carbene) Catalysts for the Arylation of Ketones
resolves10.1002/anie.200351325An N‐Heterocyclic Carbene Ligand with Flexible Steric Bulk Allows Suzuki Cross‐Coupling of Sterically Hindered Aryl Chlorides at Room Temperature
resolves10.1002/chem.200600251Easily Prepared Air‐ and Moisture‐Stable Pd–NHC (NHC=N‐Heterocyclic Carbene) Complexes: A Reliable, User‐Friendly, Highly Active Palladium Precatalyst for the Suzuki–Miyaura Reaction
resolves10.1021/om021022sPreparation of Metal−Imidazolidin-2-ylidene Complexes by Oxidative Addition
resolves10.1021/jo035834pCross-Coupling and Dehalogenation Reactions Catalyzed by (<i>N</i>-Heterocyclic carbene)Pd(allyl)Cl Complexes
resolves10.1021/om700753dSyntheses and Characterizations of Pd(II) Complexes Incorporating a <i>N</i>-Heterocyclic Carbene and Aromatic <i>N</i>-Heterocycles
resolves10.1002/asia.200800177Mono‐ and Dinuclear Palladium(II) N,S‐Heterocyclic Carbene Complexes with N Spacers and their Suzuki Coupling Activities
resolves10.1021/om1008023Dinuclear and Tetranuclear Palladium(II) Complexes of a Thiolato-Functionalized, Benzannulated N-Heterocyclic Carbene Ligand and Their Activities toward Suzuki−Miyaura Coupling
resolves10.1039/c3ra44620dGraphene oxide supported N-heterocyclic carbene-palladium as a novel catalyst for the Suzuki–Miyaura reaction
resolves10.1021/jm200187yThe Medicinal Chemist’s Toolbox: An Analysis of Reactions Used in the Pursuit of Drug Candidates
resolves10.1021/jo00979a024Palladium-catalyzed vinylic hydrogen substitution reactions with aryl, benzyl, and styryl halides
resolves10.1080/00397918108063618The Palladium-Catalyzed Cross-Coupling Reaction of Phenylboronic Acid with Haloarenes in the Presence of Bases
resolves10.1016/j.tet.2007.10.081An inexpensive and highly stable ligand 1,4-bis(2-hydroxy-3,5-di-tert-butylbenzyl)piperazine for Mizoroki–Heck and room temperature Suzuki–Miyaura cross-coupling reactions
resolves10.1016/j.poly.2012.09.020Coordination diversity of Ag(I) and Hg(II) towards symmetrically and non-symmetrically substituted imidazol-2-ylidenes: Synthesis, crystal structures, nitrile reactivity, and Hofmann-type elimination studies
resolves10.3390/molecules22030420A Palladium Catalyst System for the Efficient Cross-Coupling Reaction of Aryl Bromides and Chlorides with Phenylboronic Acid: Synthesis and Biological Activity Evaluation
resolves10.1016/j.ica.2018.04.018Palladium PEPPSI complexes: Synthesis and catalytic activity on the Suzuki-Miyaura coupling reactions for aryl bromides at room temperature in aqueous media
resolves10.1039/a608360iSynthesis and characterisation of 1-alkyl-2-imidazoline complexes of noble metals; crystal structure of trans-[PtCl2{N C(H)N(Et)CH2CH2}(PEt3)]
resolves10.1016/S0022-328X(98)00471-9Synthesis of cis- and trans-dichloro(dimethylphenylphosphine)-(1-methyl-1,4,5,6-tetrahydropyrimidine)platinum(II) and their spectral and structural characterization
The 3 references without a DOI — listed, not checked
no DOI — not checkedP. Nun, J. Martinez, F. Lamaty. Synlett, 11, 1761 (2009).
no DOI — not checkedS. Demir, I. Özdemir, O. Sahin, B. Çetinkaya, O. Büyükgüngör. Synlett, 3, 496 (2010).
no DOI — not checkedNational committee for clinical laboratory standard. Reference method for broth dilution antifungal susceptibility testing of conidium-forming filamentous fungi. Proposed standard M38-P. National committee for clinical laboratory standard Wayne (1998).
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