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 56 checked references that resolve
resolves10.1021/jo802360dLigand-Free Palladium-Catalyzed Direct Arylation of Thiazoles at Low Catalyst Loadings
resolves10.1055/s-2003-40507Recent Advances in Solution-PhaseMulticomponent Methodology for the Synthesis of HeterocyclicCompounds
resolves10.1021/cr0505728Recent Developments in Isocyanide Based Multicomponent Reactions in Applied Chemistry
resolves10.1021/ol4027073Reigoselective Arylation of Thiazole Derivatives at 5-Position via Pd Catalysis under Ligand-Free Conditions
resolves10.1021/acs.joc.9b01619Regio- and Stereoselective Synthesis of Thiazole-Containing Triarylethylenes by Hydroarylation of Alkynes
resolves10.1021/acs.orglett.5b02458Palladium-Catalyzed C–H Arylation of (Benzo)oxazoles or (Benzo)thiazoles with Aryltrimethylammonium Triflates
resolves10.1016/j.tet.2018.03.026Palladium(II)- N -heterocyclic carbene-catalyzed direct C2- or C5-arylation of thiazoles with aryl bromides
resolves10.1002/chem.201103813Palladium(II)‐Catalyzed Oxidative CH/CH Cross‐Coupling between Two Structurally Similar Azoles
resolves10.3987/COM-90-5467Palladium-catalyze Arylation of Furan, Thiophene, Benzo[b]furan and Benzo[b]thiophene
resolves10.1002/ejic.200700420Activated Aryl Chlorides: Useful Partners for the Coupling with 2‐Substituted Thiazoles in the Palladium‐Catalysed C‐H Activation/Functionalisation Reaction
resolves10.1021/acscatal.8b00440Palladium-Catalyzed Synthesis of Diaryl Ketones from Aldehydes and (Hetero)Aryl Halides via C–H Bond Activation
resolves10.1021/cr000664rAryl−Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction
resolves10.1002/cssc.201100771Solvent‐Free Palladium‐Catalyzed Direct Arylation of Heteroaromatics with Aryl Bromides
resolves10.1021/ol900159aNickel-Catalyzed Direct Arylation of Azoles with Aryl Bromides
resolves10.1039/c2cc32396fNickel catalyzed alkylation of N-aromatic heterocycles with Grignard reagents through direct C–H bond functionalization
resolves10.1002/ejoc.200500957Palladium‐ and Copper‐Mediated Direct C‐2 Arylation of Azoles — Including Free (NH)‐Imidazole, ‐Benzimidazole and ‐Indole — Under Base‐Free and Ligandless Conditions
resolves10.1002/aoc.3937Copper containing nanosilica thioalated dendritic material: A recyclable catalyst for synthesis of benzimidazoles and benzothiazoles
resolves10.1021/jo200452xLigand-Free CuO Nanospindle Catalyzed Arylation of Heterocycle C–H Bonds
resolves10.1021/ja0748985Rh(I)-Catalyzed Arylation of Heterocycles via C−H Bond Activation: Expanded Scope through Mechanistic Insight
resolves10.1016/j.jorganchem.2020.121540Palladium(II) complexes of coumarin substituted 1,2,4–triazol–5–ylidenes for catalytic C–C cross–coupling and C–H activation reactions
resolves10.1021/acs.accounts.8b00410Well-Defined Palladium(II)–NHC Precatalysts for Cross-Coupling Reactions of Amides and Esters by Selective N–C/O–C Cleavage
resolves10.1021/jo5010058<i>N</i>-Heterocyclic Carbene-Palladium(II)-1-Methylimidazole Complex-Catalyzed Direct C–H Bond Arylation of (Benz)imidazoles with Aryl Chlorides
resolves10.1002/aoc.3870New bis(<i>N</i>‐heterocyclic carbene) palladium complex immobilized on magnetic nanoparticles: as a magnetic reusable catalyst in Suzuki‐Miyaura cross coupling reaction
resolves10.1002/aoc.4280Novel (N‐heterocyclic carbene)Pd(pyridine)Br<sub>2</sub> complexes for carbonylative Sonogashira coupling reactions: Catalytic efficiency and scope for arylalkynes, alkylalkynes and dialkynes
resolves10.1002/chem.201000138Structure–Activity Relationship Analysis of Pd–PEPPSI Complexes in Cross‐Couplings: A Close Inspection of the Catalytic Cycle and the Precatalyst Activation Model
resolves10.1016/j.jorganchem.2020.121236The first used butylene linked bis(N-heterocyclic carbene)-palladium-PEPPSI complexes in the direct arylation of furan and pyrrole
resolves10.1080/00958972.2019.1572886Preparation and characterization of PEPPSI-palladium
<i>N</i>
-heterocyclic carbene complexes using benzimidazolium salts catalyzed Suzuki–Miyaura cross coupling reaction and their antitumor and antimicrobial activities
resolves10.1016/j.jorganchem.2019.06.019Synthesis and investigation of catalytic activity of phenylene – And biphenylene bridged bimetallic Palladium-PEPPSI complexes
resolves10.1016/j.ica.2019.118969Synthesis of bridged palladium-PEPPSI complexes and catalytic studies in C–C cross-coupling reactions
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
resolves10.1016/j.ica.2017.09.048Sonogashira cross-coupling reaction catalyzed by N-heterocyclic carbene-Pd(II)-PPh3 complexes under copper free and aerobic conditions
resolves10.1002/aoc.4936Well‐Defined N‐Heterocyclic Carbene‐Palladium Complexes as Efficient Catalysts for Domino Sonogashira Coupling/Cyclization Reaction and C‐H bond Arylation of Benzothiazole
resolves10.1007/s10593-019-02445-1Adamantanyl-substituted PEPPSI-type palladium(II) N-heterocyclic carbene complexes: synthesis and catalytic application for CH activation of substituted thiophenes
resolves10.1021/acs.organomet.0c00494Direct (Hetero)arylation of Heteroarenes Catalyzed by Unsymmetrical Pd-PEPPSI-NHC Complexes under Mild Conditions
resolves10.1021/acs.joc.0c02024Well-Defined Palladium N-Heterocyclic Carbene Complexes: Direct C–H Bond Arylation of Heteroarenes
resolves10.1002/aoc.5869Benzimidazole bearing Pd–PEPPSI complexes catalyzed direct C2‐arylation/heteroarylation of<i>N</i>‐substituted benzimidazoles
resolves10.1016/j.molstruc.2019.127608New Pd-PEPPSI complexes bearing meta-cyanobenzyl-Substituted NHC: Synthesis, characterization, crystal structure and catalytic activity in direct C–H arylation of (Hetero)arenes with aryl bromides
resolves10.1021/ol027190yPalladium Catalysts for Aerobic Oxidative Kinetic Resolution of Secondary Alcohols Based on Mechanistic Insight
resolves10.1039/C7NJ00488ESynthesis and catalytic applications of palladium N-heterocyclic carbene complexes as efficient pre-catalysts for Suzuki–Miyaura and Sonogashira coupling reactions
resolves10.1021/ol0702324Palladium-Catalyzed Arylation of Electron-Rich Heterocycles with Aryl Chlorides
resolves10.1016/j.jorganchem.2016.12.026Reactivity of N-protected 5-(2-bromophenyl)tetrazoles in palladium-catalyzed direct arylation of heteroarenes or fluorobenzenes
resolves10.1039/c3cy00150dDirect heteroarylation of 5-bromothiophen-2-ylpyridine and of 8-bromoquinoline via palladium-catalysed C–H bond activation: simpler access to heteroarylated nitrogen-based derivatives
resolves10.1002/cctc.201200867Palladium‐Catalysed Regioselective Direct Arylations of Heteroarenes by Bromobenzamides: Direct Synthesis of Heteroaryl Benzamides
resolves10.1039/c1ra00370dPalladium-catalysed direct polyheteroarylation of di- or tribromobenzene derivatives: a one step synthesis of conjugated poly(hetero)aromatics
resolves10.1021/jo201516vPalladium-Catalyzed Direct Arylation of Heteroaromatic Compounds: Improved Conditions Utilizing Controlled Microwave Heating
resolves10.1039/c0gc00229aCarbonates: eco-friendly solvents for palladium-catalysed direct arylation of heteroaromatics
resolves10.1002/ejoc.201402586A Robust and Efficient Catalyst Possessing an Electron‐Deficient Ligand for the Palladium‐Catalyzed Direct Arylation of Heteroarenes
resolves10.1039/C7OB00856BCamphyl-based α-diimine palladium complexes: highly efficient precatalysts for direct arylation of thiazoles in open-air
resolves10.1016/j.jorganchem.2019.06.016Direct C-H bond (Hetero)arylation of thiazole derivatives at 5-position catalyzed by N-heterocyclic carbene palladium complexes at low catalyst loadings under aerobic conditions
checked 2026-07-23 — re-checked daily as this page is visited;
titles and statuses come from Crossref and DataCite and are not part of the signed record
Both snippets point at the live badge image and link back to this page. The
badge re-renders from the daily check, so an embed never goes stale by more than a day of visits.