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Ru(II)-Catalyzed Synthesis of Fused Imidazo[1,2-a]pyridine-chromenones and Methylene-Tethered Bis-imidazo[1,2-a]pyridines and Regioselective O-Acetoxylation of Imidazo[1,2-a]pyridines

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What this work says

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

inferredcites →https://doi.org/10.1002/adsc.201600067openalex-snapshot
N,N‐Dimethylacetamide (DMA) as a Methylene Synthon for Regioselective Linkage of Imidazo[1,2‐a]pyridine
inferredcites →https://doi.org/10.1002/adsc.201800755openalex-snapshot
Recent Advances in Ruthenium(II)‐Catalyzed C−H Bond Activation and Alkyne Annulation Reactions
inferredcites →https://doi.org/10.1002/ajoc.202100225openalex-snapshot
Regioselective Base‐controlled Pd‐catalyzed Arylation of Imidazo[1,2‐a]pyridines: leading selectivity at C8 position by N‐chelation over O‐chelation
inferredcites →https://doi.org/10.1002/anie.201403453openalex-snapshot
A Metal‐Free Three‐Component Reaction for the Regioselective Synthesis of 1,4,5‐Trisubstituted 1,2,3‐Triazoles
inferredcites →https://doi.org/10.1002/anie.201405457openalex-snapshot
Efficient Disproportionation of Formic Acid to Methanol Using Molecular Ruthenium Catalysts
inferredcites →https://doi.org/10.1002/anie.202104503openalex-snapshot
KIO4‐mediated Selective Hydroxymethylation/Methylenation of Imidazo‐Heteroarenes: A Greener Approach
inferredcites →https://doi.org/10.1002/cjoc.201900468openalex-snapshot
Ni‐Catalyzed Chelation‐Assisted Direct Functionalization of Inert C—H Bonds
inferredcites →https://doi.org/10.1002/ejoc.202000467openalex-snapshot
Polyethylene Glycol (PEG‐400) as Methylene Spacer and Green Solvent for the Synthesis of Heterodiarylmethanes under Metal‐Free Conditions
inferredcites →https://doi.org/10.1016/j.bmc.2019.06.033openalex-snapshot
Rational approaches, design strategies, structure activity relationship and mechanistic insights for therapeutic coumarin hybrids
inferredcites →https://doi.org/10.1016/j.bmcl.2008.12.098openalex-snapshot
Synthesis of hydroxycoumarins and hydroxybenzo[f]- or [h]coumarins as lipid peroxidation inhibitors
inferredcites →https://doi.org/10.1016/j.cclet.2021.10.019openalex-snapshot
Palladium-catalyzed relay C–H functionalization to construct novel hybrid-arylcyclophosphorus ligand precursors
inferredcites →https://doi.org/10.1016/j.cclet.2022.107894openalex-snapshot
Phosphine oxide directing-group-enabled atroposelective C–H bond acyloxylation via an eight-membered palladacycle intermediate
inferredcites →https://doi.org/10.1016/j.ejmcr.2022.100038openalex-snapshot
Recent advances on anticancer activity of coumarin derivatives
inferredcites →https://doi.org/10.1016/j.ejmech.2019.111587openalex-snapshot
Coumarin-containing hybrids and their anticancer activities
inferredcites →https://doi.org/10.1016/j.ejphar.2009.03.027openalex-snapshot
Effects of umbelliferone in a murine model of allergic airway inflammation
inferredcites →https://doi.org/10.1016/j.mcat.2017.06.021openalex-snapshot
Ruthenium-catalysed decomposition of formic acid: Fuel cell and catalytic applications
inferredcites →https://doi.org/10.1016/j.tetlet.2019.151162openalex-snapshot
CuI-catalyzed highly regioselective C H functionalization of indoles using indole-3-tosylhydrazones as carbene precursor: An efficient synthesis of 3,3-bis(indolyl)methane derivatives
inferredcites →https://doi.org/10.1016/j.tube.2020.102050openalex-snapshot
Coumarin hybrid derivatives as promising leads to treat tuberculosis: Recent developments and critical aspects of structural design to exhibit anti-tubercular activity
inferredcites →https://doi.org/10.1021/acs.jmedchem.5b01380openalex-snapshot
Artemisinin-Derived Dimers: Potent Antimalarial and Anticancer Agents
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00391openalex-snapshot
Anisucoumaramide, a Bioactive Coumarin from Clausena anisum-olens
inferredcites →https://doi.org/10.1021/acs.joc.1c02811openalex-snapshot
Directed Palladium-Catalyzed Acetoxylation of Indolines. Total Synthesis of N -Benzoylcylindrocarine
inferredcites →https://doi.org/10.1021/acs.joc.6b00166openalex-snapshot
Synthesis of Indeno[1′,2′:4,5]imidazo[1,2-a]pyridin-11-ones and Chromeno[4′,3′:4,5]imidazo[1,2-a]pyridin-6-ones through Palladium-Catalyzed Cascade Reactions of 2-(2-Bromophenyl)imidazo[1,2-a]pyridines
inferredcites →https://doi.org/10.1021/acs.joc.6b02850openalex-snapshot
Substrate-Controlled Regioselective Arylations of 2-Indolylmethanols with Indoles: Synthesis of Bis(indolyl)methane and 3,3′-Bisindole Derivatives
inferredcites →https://doi.org/10.1021/acs.joc.7b02203openalex-snapshot
Rhodium-Catalyzed sp2 C–H Acetoxylation of N-Aryl Azaindoles/N-Heteroaryl Indolines
inferredcites →https://doi.org/10.1021/acs.joc.9b00729openalex-snapshot
Formation of Methylene Linkage for N-Heterocycles: Sequential C–H and C–O Bond Functionalization of Methanol with Cosolvent Water
inferredcites →https://doi.org/10.1021/acs.joc.9b03197openalex-snapshot
Direct Oxygenation of C–H Bonds through Photoredox and Palladium Catalysis
inferredcites →https://doi.org/10.1021/acs.orglett.6b00268openalex-snapshot
Ruthenium-Catalyzed Regioselective C–H Bond Acetoxylation on Carbazole and Indole Frameworks
inferredcites →https://doi.org/10.1021/acs.orglett.6b03601openalex-snapshot
Transition-Metal-Free Lactonization of sp2 C–H Bonds with CO2
inferredcites →https://doi.org/10.1021/acsomega.9b00035openalex-snapshot
BCl3-Mediated C–N, C–S, and C–O Bond Formation of Imidazo[1,2- a ]pyridine Benzylic Ethers
inferredcites →https://doi.org/10.1021/ar7000843openalex-snapshot
Hybrid Molecules with a Dual Mode of Action: Dream or Reality?
inferredcites →https://doi.org/10.1021/jm00327a007openalex-snapshot
Derivatives of Imidazole. I. Synthesis and Reactions of Imidazo[1,2-α]pyridines with Analgesic, Antiinflammatory, Antipyretic, and Anticonvulsant Activity
inferredcites →https://doi.org/10.1021/jm0580149openalex-snapshot
Synthesis and Antiinflammatory Activity of Coumarin Derivatives,
inferredcites →https://doi.org/10.1021/jm200148popenalex-snapshot
Engineering an Antibiotic to Fight Cancer: Optimization of the Novobiocin Scaffold to Produce Anti-proliferative Agents
inferredcites →https://doi.org/10.1038/nrd3554openalex-snapshot
Interfering with pH regulation in tumours as a therapeutic strategy
inferredcites →https://doi.org/10.1039/c4cy00231hopenalex-snapshot
Regioselective catalytic acetoxylation of limonene
inferredcites →https://doi.org/10.1039/c5ob00776copenalex-snapshot
CuBr catalyzed aerobic oxidative coupling of 2-aminopyridines with cinnamaldehydes: direct access to 3-formyl-2-phenyl-imidazo[1,2-a]pyridines
inferredcites →https://doi.org/10.1039/d0qo00702aopenalex-snapshot
Transition-metal-free highly regioselective C–H acetoxylation of pyrrolo[2,3- d ]pyrimidine derivatives
inferredcites →https://doi.org/10.1039/d1ob01683kopenalex-snapshot
Palladium( ii ) catalyzed site-selective C–H olefination of imidazo[1,2- a ]pyridines
inferredcites →https://doi.org/10.1111/j.1527-3466.2002.tb00085.xopenalex-snapshot
Olprinone: A Phosphodiesterase III Inhibitor with Positive Inotropic and Vasodilator Effects
inferredcites →https://doi.org/10.1503/jpnopenalex-snapshot
Journal of Psychiatry and Neuroscience
inferredcites →https://doi.org/10.2174/138955707781662645openalex-snapshot
Recent Progress in the Pharmacology of Imidazo[1,2-a]pyridines
inferredcites →https://doi.org/10.3390/molecules25235685openalex-snapshot
Promising Lead Compounds in the Development of Potential Clinical Drug Candidate for Drug-Resistant Tuberculosis
inferredcites →https://doi.org/10.4155/fmc-2018-0375openalex-snapshot
Translational Role of Natural Coumarins and Their Derivatives As Anticancer Agents

What points at this work

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

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inferred← citeshttps://doi.org/10.1016/j.gresc.2026.02.002openalex-snapshot
Iridium-catalyzed C(sp3)-H activation using imidazopyridine and pyridine as directing groups for selective silylation
inferred← citeshttps://doi.org/10.1016/j.jics.2024.101561openalex-snapshot
An efficient and sustainable multicomponent synthesis of structurally diverse tetrahydrochromeno[2,3-c]pyrazol-5(1H)-one using indium triflate as a reusable catalyst
inferred← citeshttps://doi.org/10.1016/j.tet.2024.133943openalex-snapshot
HFIP-promoted synthesis of imidazo [1,2-a]pyridines containing CF3-substituted tertiary alcohols at room temperature
inferred← citeshttps://doi.org/10.1021/acs.analchem.5c01078openalex-snapshot
Chronofluorometry Based on a Facile Fluorescent Probe for Rapid Detection of Fractional Exhaled Nitric Oxide and Bioimaging in Live Cells
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02938openalex-snapshot
Base-Catalyzed Aqueous Methylenation of Imidazo[1,2- a ]pyridines with Glyoxylic Acid: Synthesis of Bis(imidazo[1,2- a ]pyridin-3-yl)methanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03592openalex-snapshot
Skeletal Editing Via CH→N Atom Swapping in Fused Imidazoles: Access to Triazolo[5,1- a ]isoquinoline, Triazolo[1,5- a ]quinoline, and Triazolo-[1,5- a ]pyridines Frameworks
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03934openalex-snapshot
Ruthenium-Catalyzed C(sp 2 )–H Activation Using Pyridine and Imidazopyridine as Directing Groups for Selective Silylation
inferred← citeshttps://doi.org/10.1039/d3ob00849eopenalex-snapshot
Synthesis and site selective C–H functionalization of imidazo-[1,2- a ]pyridines
inferred← citeshttps://doi.org/10.1039/d4dt00380bopenalex-snapshot
DLPNO-CCSD(T) and DFT study of the acetate-assisted C–H activation of benzaldimine at [RuCl 2 ( p -cymene)] 2 : the relevance of ligand exchange processes at ruthenium( ii ) complexes in polar protic media
inferred← citeshttps://doi.org/10.1039/d5sc00449gopenalex-snapshot
Harnessing C–H acetoxylation: a gateway to oxygen-enriched organic frameworks
inferred← citeshttps://doi.org/10.2139/ssrn.5126177openalex-snapshot
The Sulfuration of Imidazopyridines with Sulfinic Acids Mediated by Dtbp/Hcl
inferred← citeshttps://doi.org/10.3390/molecules30030607openalex-snapshot
Recent Advances in Visible Light-Induced C-H Functionalization of Imidazo[1,2-a]pyridines
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