On the public citation graph

Highly Selective Room-Temperature Suzuki–Miyaura Coupling of Bromo-2-sulfonyloxypyridines for Unsymmetrical Diarylpyridines

https://doi.org/10.1021/acs.joc.0c00793
0 signed · 76 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/14651858.cd004309.pub3openalex-snapshot
Single dose oral etoricoxib for acute postoperative pain in adults
inferredcites →https://doi.org/10.1002/adsc.201200583openalex-snapshot
2‐(1‐Benzotriazolyl)pyridine: A Robust Bidentate Ligand for the Palladium‐Catalyzed CC (Suzuki, Heck, Fujiwara–Moritani, Sonogashira), CN and CS Coupling Reactions
inferredcites →https://doi.org/10.1002/adsc.201600950openalex-snapshot
Synthesis of Trisubstituted Pyridines via Chemoselective Suzuki–Miyaura Coupling of 3,5‐ and 4,6‐Dibromo‐2‐tosyloxypyridines
inferredcites →https://doi.org/10.1002/anie.200900465openalex-snapshot
Devising Boron Reagents for Orthogonal Functionalization through Suzuki–Miyaura Cross‐Coupling
inferredcites →https://doi.org/10.1002/anie.201107017openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling: A Historical Contextual Perspective to the 2010 Nobel Prize
inferredcites →https://doi.org/10.1002/anie.201609635openalex-snapshot
Rapid Room‐Temperature, Chemoselective C−C Coupling of Poly(pseudo)halogenated Arenes Enabled by Palladium(I) Catalysis in Air
inferredcites →https://doi.org/10.1002/anie.201906080openalex-snapshot
Selective Late‐Stage Oxygenation of Sulfides with Ground‐State Oxygen by Uranyl Photocatalysis
inferredcites →https://doi.org/10.1002/chem.201600167openalex-snapshot
Chemoselective Synthesis of Polysubstituted Pyridines from Heteroaryl Fluorosulfates
inferredcites →https://doi.org/10.1002/ejoc.201201575openalex-snapshot
Highly Fluorescent, π‐Extended Indenopyrido[2,1‐a]isoindolone Derivatives Prepared by a Palladium‐Catalysed Cascade Reaction
inferredcites →https://doi.org/10.1002/ejoc.201300592openalex-snapshot
Palladium(II) Catalyzed Suzuki/Sonogashira Cross‐Coupling Reactions of Sulfonates: An Efficient Approach to C2‐Functionalized Pyrimidines and Pyridines
inferredcites →https://doi.org/10.1002/ejoc.201701718openalex-snapshot
Chemoselective Synthesis of Arylpyridines through Suzuki–Miyaura Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/jlcr.2580360808openalex-snapshot
Synthesis of [4,6‐3H]‐2‐pyridone and [3H]‐RS‐91309
inferredcites →https://doi.org/10.1002/slct.201703073openalex-snapshot
Chemoselective Suzuki Coupling of Bromoarenes Catalysed by Palladium(II)‐Complexing Macrocycles in Aqueous Media
inferredcites →https://doi.org/10.1007/3-540-45313-x_2openalex-snapshot
Organoboron Compounds
inferredcites →https://doi.org/10.1016/j.bmcl.2010.01.045openalex-snapshot
Discovery of N-(5,6-diarylpyridin-2-yl)amide derivatives as potent and selective A2B adenosine receptor antagonists
inferredcites →https://doi.org/10.1016/j.dyepig.2012.11.014openalex-snapshot
Synthesis and characterization of highly stable and efficient star-molecules
inferredcites →https://doi.org/10.1016/j.ejmech.2012.01.015openalex-snapshot
Dihydroxylated 2,4,6-triphenyl pyridines: Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure–activity relationship study
inferredcites →https://doi.org/10.1016/j.jphotobiol.2013.08.016openalex-snapshot
Bioimaging, antibacterial and antifungal properties of imidazole-pyridine fluorophores: Synthesis, characterization and solvatochromism
inferredcites →https://doi.org/10.1016/j.tet.2013.10.065openalex-snapshot
Palladium-catalyzed highly regioselective 2-arylation of 2,x-dibromopyridines and its application in the efficient synthesis of a 17β-HSD1 inhibitor
inferredcites →https://doi.org/10.1016/j.tetlet.2007.05.121openalex-snapshot
Nakinadine A, a novel bis-pyridine alkaloid with a β-amino acid moiety from sponge Amphimedon sp.
inferredcites →https://doi.org/10.1016/s0040-4039(01)95429-2openalex-snapshot
A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides
inferredcites →https://doi.org/10.1016/s0960-894x(01)00321-3openalex-snapshot
2-Amino-4,6-diarylpyridines as novel ligands for the estrogen receptor
inferredcites →https://doi.org/10.1016/s0960-894x(98)00499-5openalex-snapshot
2-Pyridinyl-3-(4-methylsulfonyl)phenylpyridines: Selective and orally active cyclooxygenase-2 inhibitors
inferredcites →https://doi.org/10.1021/acs.jmedchem.5b01935openalex-snapshot
4,6-Diphenylpyridines as Promising Novel Anti-Influenza Agents Targeting the PA–PB1 Protein–Protein Interaction: Structure–Activity Relationships Exploration with the Aid of Molecular Modeling
inferredcites →https://doi.org/10.1021/acs.joc.7b00550openalex-snapshot
Palladium Catalyzed Arylation and Benzylation of Nitroarenes Using Aryl Sulfonates and Benzyl Acetates
inferredcites →https://doi.org/10.1021/cm0010250openalex-snapshot
An Efficient Pyridine- and Oxadiazole-Containing Hole-Blocking Material for Organic Light-Emitting Diodes: Synthesis, Crystal Structure, and Device Performance
inferredcites →https://doi.org/10.1021/cm703682qopenalex-snapshot
Pyridine-Containing Bipolar Host Materials for Highly Efficient Blue Phosphorescent OLEDs
inferredcites →https://doi.org/10.1021/cr00039a007openalex-snapshot
Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
inferredcites →https://doi.org/10.1021/cr100327popenalex-snapshot
Advances in Transition Metal (Pd,Ni,Fe)-Catalyzed Cross-Coupling Reactions Using Alkyl-organometallics as Reaction Partners
inferredcites →https://doi.org/10.1021/cr60111a001openalex-snapshot
Heterocyclic Nitrogen Compounds. Part IIA. Hexacyclic Compounds: Pyridine, Quinoline, and Isoquinoline.
inferredcites →https://doi.org/10.1021/ja031936lopenalex-snapshot
Homogeneous Palladium Catalyst Suppressing Pd Black Formation in Air Oxidation of Alcohols
inferredcites →https://doi.org/10.1021/ja036947topenalex-snapshot
The First General Palladium Catalyst for the Suzuki−Miyaura and Carbonyl Enolate Coupling of Aryl Arenesulfonates
inferredcites →https://doi.org/10.1021/jacs.8b09595openalex-snapshot
Heterocyclic Allylsulfones as Latent Heteroaryl Nucleophiles in Palladium-Catalyzed Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/jm200187yopenalex-snapshot
The Medicinal Chemist’s Toolbox: An Analysis of Reactions Used in the Pursuit of Drug Candidates
inferredcites →https://doi.org/10.1021/jm500002kopenalex-snapshot
Design, Synthesis, and Biological Evaluation of Novel Pyridine-Bridged Analogues of Combretastatin-A4 as Anticancer Agents
inferredcites →https://doi.org/10.1021/jo400695copenalex-snapshot
Syntheses of (+)-Complanadine A and Lycodine Derivatives by Regioselective [2 + 2 + 2] Cycloadditions
inferredcites →https://doi.org/10.1021/jo402200qopenalex-snapshot
Fully Regiocontrolled Polyarylation of Pyridine
inferredcites →https://doi.org/10.1021/jo701709aopenalex-snapshot
Disubstituted Pyridines: The Double-Coupling Approach
inferredcites →https://doi.org/10.1021/jo900292bopenalex-snapshot
Ring-Closing Metathesis Reactions on Azinium Salts: Straightforward Access to Quinolizinium Cations and Their Dihydro Derivatives
inferredcites →https://doi.org/10.1021/jo902015wopenalex-snapshot
Zinc Chloride-Promoted Aryl Bromide−Alkyne Cross-Coupling Reactions at Room Temperature
inferredcites →https://doi.org/10.1021/ol006097bopenalex-snapshot
Annulation of Ketones with Vinamidinium Hexafluorophosphate Salts: An Efficient Preparation of Trisubstituted Pyridines
inferredcites →https://doi.org/10.1021/ol016526lopenalex-snapshot
NiCl2(PCy3)2: A Simple and Efficient Catalyst Precursor for the Suzuki Cross-Coupling of Aryl Tosylates and Arylboronic Acids
inferredcites →https://doi.org/10.1021/ol025673wopenalex-snapshot
Facile Pd-Catalyzed Cross-Coupling of 2‘-Deoxyguanosine O6-Arylsulfonates with Arylboronic Acids
inferredcites →https://doi.org/10.1021/ol100008qopenalex-snapshot
Pd-Catalyzed Decarboxylative Cross Coupling of Potassium Polyfluorobenzoates with Aryl Bromides, Chlorides, and Triflates
inferredcites →https://doi.org/10.1021/ol900358nopenalex-snapshot
One-Pot Double Suzuki−Miyaura Couplings: Rapid Access to Nonsymmetrical Tri(hetero)aryl Derivatives
inferredcites →https://doi.org/10.1021/op020085jopenalex-snapshot
The Development of a Practical and Reliable Large-Scale Synthesis of 2,6-Diamino-4-bromopyridine
inferredcites →https://doi.org/10.1039/a707613dopenalex-snapshot
Pyrrole, pyrrolidine, pyridine, piperidine and tropane alkaloids (1998 to 1999)
inferredcites →https://doi.org/10.1039/b413750gopenalex-snapshot
Quinoline, quinazoline and acridone alkaloids
inferredcites →https://doi.org/10.1039/b515168fopenalex-snapshot
Regioselective functionalization of trisubstituted pyridines using a bromine–magnesium exchange
inferredcites →https://doi.org/10.1039/c39790000866openalex-snapshot
Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst
inferredcites →https://doi.org/10.1039/c3sc50155hopenalex-snapshot
Clathrochelate-based bipyridyl ligands of nanoscale dimensions: easy-to-access building blocks for supramolecular chemistry
inferredcites →https://doi.org/10.1039/c5ob00866bopenalex-snapshot
Synthesis of tetraarylpyridines by chemo-selective Suzuki–Miyaura reactions of 3,5-dibromo-2,6-dichloropyridine
inferredcites →https://doi.org/10.1039/c6sc02118bopenalex-snapshot
Site-selective Suzuki–Miyaura coupling of heteroaryl halides – understanding the trends for pharmaceutically important classes
inferredcites →https://doi.org/10.1039/c8ta12206gopenalex-snapshot
Pyridine-functionalized fullerene additive enabling coordination interactions with CH 3 NH 3 PbI 3 perovskite towards highly efficient bulk heterojunction solar cells
inferredcites →https://doi.org/10.1055/s-0035-1560392openalex-snapshot
A Novel Convenient Synthesis of Pyridinyl and Quinolinyl Triflates and Tosylates via One-Pot Diazotization of Aminopyridines and Aminoquinolines in Solution
inferredcites →https://doi.org/10.1124/pr.55.3.4openalex-snapshot
Specific Targeted Therapy of Chronic Myelogenous Leukemia with Imatinib
inferredcites →https://doi.org/10.1358/dof.2001.026.04.616043openalex-snapshot
Etoricoxib
inferredcites →https://doi.org/10.2165/00003495-200565160-00010openalex-snapshot
Atazanavir

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4651066openalex-extracted
An Environmentally Benign Radical Annulation of Α,Β-Unsaturated Ketoxime Acetates with 3-Formylchromones for the Synthesis of Functionalized 2,4-Diarylpyridines
inferred← citeshttps://doi.org/10.1002/adsc.202101514openalex-snapshot
Protecting Group‐Controlled Regioselective Synthesis for Unsymmetrical 3,5‐Disubstituted Pyridones
inferred← citeshttps://doi.org/10.1002/adsc.202201194openalex-snapshot
Regioselective Ortho‐Arylation of Polyhalo‐Substituted (Hetero)Aryl Tosylates Using an Integrated Continuous Flow/Batch Protocol
inferred← citeshttps://doi.org/10.1002/ange.202410297openalex-snapshot
Radical 6‐Endo Addition Enables Pyridine Synthesis under Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1002/anie.202410297openalex-snapshot
Radical 6‐Endo Addition Enables Pyridine Synthesis under Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1002/bkcs.12717openalex-snapshot
Integrated continuous‐flow/batch protocol for ortho‐selective alkynylation of (hetero)aryl tosylates
inferred← citeshttps://doi.org/10.1002/slct.202201441openalex-snapshot
Derivatization of Marine‐Derived Fascaplysin via Highly Regioselective Suzuki‐Miyaura Coupling Contributing to the Enhanced Antibacterial Activity
inferred← citeshttps://doi.org/10.1016/j.comptc.2022.113910openalex-snapshot
Theoretical study of the one- and two-photon absorption cross-section of substituted polyaryl pyridine-based compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133468openalex-snapshot
Synthesis of 2,5-difunctionalized pyridines via sequential chemoselective amination and Suzuki–Miyaura reactions
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02770openalex-snapshot
Visible Light-Induced Divergent Deoxygenation/Hydroxymethylation of Pyridine N-Oxides
inferred← citeshttps://doi.org/10.1021/acs.organomet.3c00231openalex-snapshot
Homogeneous and Recyclable Palladium Catalysts: Application in Suzuki–Miyaura Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/acs.organomet.5c00462openalex-snapshot
Palladacycle Catalyst Based on a Cyclopropane Monophosphine Ligand for the Suzuki–Miyaura Cross-Coupling Reaction
inferred← citeshttps://doi.org/10.1039/d3qo00640aopenalex-snapshot
Recent advances in the application of ligands in palladium-catalyzed chemoselective coupling reactions at C–Br, C–OTf, and C–Cl sites
inferred← citeshttps://doi.org/10.1039/d3qo00685aopenalex-snapshot
Fe(OTf) 3 -catalyzed annulation of α,β-unsaturated ketoxime acetates with enaminones for the synthesis of functionalized 2,4-diarylpyridines
inferred← citeshttps://doi.org/10.1039/d3qo00891fopenalex-snapshot
Modular synthesis of unsymmetric 2,4-diaryl-substituted pyridines through a four-component cyclization strategy under metal-free conditions
inferred← citeshttps://doi.org/10.1039/d4nj01648copenalex-snapshot
Cu( ii )-catalyzed annulation of α,β-unsaturated ketoxime acetates with 3-formylchromones for the synthesis of functionalized 2,4-diarylpyridines
inferred← citeshttps://doi.org/10.1039/d5re00486aopenalex-snapshot
Homogeneous catalysis in liquid organic hydrogen carriers: advances, challenges, and future directions
inferred← citeshttps://doi.org/10.1155/joch/6253535openalex-snapshot
Advances in Palladium‐Catalyzed Suzuki–Miyaura Cross‐Coupling Strategies for Heterocyclic Synthesis: Focus on Pyridines, Indoles, and Quinolines
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.