On the public citation graph

Imidazo[1,2-a]pyridine anthelmintic and antifungal agents

https://doi.org/10.1021/jm00279a026
0 signed · 225 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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 points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4524815openalex-extracted
inferred← citeshttps://doi.org/10.1002/9780470187005.ch2openalex-snapshot
Indolizine and Aza Derivatives With Additional Nitrogens in the 5‐Membered Ring
inferred← citeshttps://doi.org/10.1002/9781118336953.ch5openalex-snapshot
Fluorous Synthesis of 3‐Aminoimidazo[1,2‐ a ]‐Pyridine/Pyrazine Library
inferred← citeshttps://doi.org/10.1002/adsc.201201112openalex-snapshot
Iron(III)‐Catalyzed Cascade Reaction between Nitroolefins and 2‐Aminopyridines: Synthesis of Imidazo[1,2‐a]pyridines and Easy Access towards Zolimidine
inferred← citeshttps://doi.org/10.1002/adsc.201300996openalex-snapshot
Gold‐Catalyzed Redox Synthesis of Imidazo[1,2‐ a ]pyridines using Pyridine N ‐Oxide and Alkynes
inferred← citeshttps://doi.org/10.1002/adsc.201501012openalex-snapshot
2‐Aminopyridines as an α‐Bromination Shuttle in a Transition Metal‐Free One‐Pot Synthesis of Imidazo[1,2‐a]pyridines
inferred← citeshttps://doi.org/10.1002/adsc.201600225openalex-snapshot
Vanadyl Acetylacetonate Catalyzed Methylenation of Imidazo[1,2‐a]pyridines by Using Dimethylacetamide as a Methylene Source: Direct Access to Bis(imidazo[1,2‐a]pyridin‐3‐yl)methanes
inferred← citeshttps://doi.org/10.1002/adsc.201800531openalex-snapshot
External Oxidant‐Free Regioselective Cross Dehydrogenative Coupling of 2‐Arylimidazoheterocycles and Azoles with H2 Evolution via Photoredox Catalysis
inferred← citeshttps://doi.org/10.1002/ajoc.201500297openalex-snapshot
Synthesis of Naphtho‐Fused Imidazo[1,2‐a]pyridines through Copper‐Catalyzed Cascade Reactions
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/aoc.4692openalex-snapshot
Ru(II)‐based antineoplastic: A “wingtip” N‐heterocyclic carbene facilitates access to a new class of organometallics that are cytotoxic to common cancer cell lines
inferred← citeshttps://doi.org/10.1002/aoc.6031openalex-snapshot
CuI/Fe 3 O 4 NPs@Biimidazole IL‐KCC‐1 as a leach proof nanocatalyst for the synthesis of imidazo[1,2‐ a ]pyridines in aqueous medium
inferred← citeshttps://doi.org/10.1002/aoc.70124openalex-snapshot
Integrated Experimental and Computational Study of Imidazopyridine Derivatives: Synthesis, DFT, Molecular Docking and Dynamic Simulations
inferred← citeshttps://doi.org/10.1002/aoc.7903openalex-snapshot
Discovery of Imidazo[1,2‐a]pyrimidine–Schiff Base Derivatives as Potent Antifungal Agents Against Fusarium oxysporum f. sp. albedinis: Synthesis, Crystal Structure, Biological Evaluation, Homology Modeling, and Docking Analysis
inferred← citeshttps://doi.org/10.1002/asia.202500455openalex-snapshot
Visible Light‐Mediated Preparation of a Key Intermediate Employed in the Synthesis of Zolpidem and Several Analogs
inferred← citeshttps://doi.org/10.1002/cber.19901230218openalex-snapshot
Imidazole Derivatives, III. Regiospecific Synthesis,Structure, and Fluorescence Properties of Highly substituted Imidazo[1,2‐a]pyridines and Pyrido[1,2‐a]benzimidazoles
inferred← citeshttps://doi.org/10.1002/chin.197304320openalex-snapshot
ChemInform Abstract: IMIDAZO(1,2‐A)PYRIDIN‐ANTHELMINTICA UND FUNGICIDE
inferred← citeshttps://doi.org/10.1002/cjoc.200990060openalex-snapshot
Tin(II) Chloride Dihydrate Catalyzed Groebke Condensation: An Efficient Protocol for the Synthesis of 3‐Aminoimidazo[1,2‐a]pyridines
inferred← citeshttps://doi.org/10.1002/ejoc.201300905openalex-snapshot
Aerobic Multicomponent Tandem Synthesis of 3‐Sulfenylimidazo[1,2‐a]pyridines from Ketones, 2‐Aminopyridines, and Disulfides
inferred← citeshttps://doi.org/10.1002/ejoc.201301612openalex-snapshot
One‐Pot Synthesis of N‐(Imidazo[1,2‐a]pyridin‐3‐yl)‐Substituted Sulfonamides Using Catalytic Zinc Chloride
inferred← citeshttps://doi.org/10.1002/ejoc.201400065openalex-snapshot
Functionalization of Imidazo[1,2‐a]pyridines by Means of Metal‐Catalyzed Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.201600485openalex-snapshot
Highly Efficient and Practical Thiocyanation of Imidazopyridines Using an N ‐Chlorosuccinimide/NaSCN Combination
inferred← citeshttps://doi.org/10.1002/ejoc.201700496openalex-snapshot
One‐Pot Synthesis of Naphtho[1′,2′:4,5]imidazo[1,2‐a]pyridin‐5‐yl(aryl)methanones through Sequential Sonogashira Coupling/Alkyne–Carbonyl Metathesis
inferred← citeshttps://doi.org/10.1002/ejoc.201901748openalex-snapshot
Pd‐Catalyzed ortho Selective C–H Acyloxylation and Hydroxylation of Pyridotriazoles
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/ejoc.202400022openalex-snapshot
B(C 6 F 5 ) 3 ‐Catalysed Alkylation of Imidazo[1,2‐ a ]pyridines Using α , β ‐Unsaturated Ketones
inferred← citeshttps://doi.org/10.1002/ejoc.70733openalex-snapshot
DMDM Hydantoin as C1 Precursor for Solvent‐Controlled C‐3 Hydroxymethylation and Methylenation of Imidazo[1,2‐ a ]pyridines
inferred← citeshttps://doi.org/10.1002/jccs.200400201openalex-snapshot
Hypervalent Iodine(III) Sulfonate Mediated Synthesis of Imidazo[1,2‐a]pyridines
inferred← citeshttps://doi.org/10.1002/jccs.201000024openalex-snapshot
Iodobenzene‐Catalyzed Synthesis of Imidazo[1,2‐a]pyridines from Aryl Ketones with mCPBA in Ionic Liquid
inferred← citeshttps://doi.org/10.1002/jccs.202000468openalex-snapshot
Room temperature ionic liquid promoted improved and rapid synthesis of highly functionalized imidazole and evaluation of their inhibitory activity against human cancer cells
inferred← citeshttps://doi.org/10.1002/jhet.3140openalex-snapshot
Design and Synthesis of Imidazo[1,2‐a]pyridines with Carboxamide Group Substitution andIn silicoEvaluation of their Interaction with a LuxR‐type Quorum Sensing Receptor
inferred← citeshttps://doi.org/10.1002/jhet.4106openalex-snapshot
A simple and efficient route to 2‐arylimidazo[1,2‐a]pyridines and zolimidine using automated grindstone chemistry
inferred← citeshttps://doi.org/10.1002/jhet.4164openalex-snapshot
Solvent and catalyst‐free synthesis of imidazo[1,2‐a]pyridines by grindstone chemistry
inferred← citeshttps://doi.org/10.1002/jhet.4259openalex-snapshot
Design, synthesis, anticancer activity, and in silico studies of novel imidazo[1,2‐ a ]pyridine based 1 H ‐1,2,3‐triazole derivatives
inferred← citeshttps://doi.org/10.1002/jhet.5570210640openalex-snapshot
Synthèse de dérivés imidazopyridiniques et pyridinotriaziniques
inferred← citeshttps://doi.org/10.1002/jhet.5570290636openalex-snapshot
Methyl imidazo[1,2‐b]pyridazine‐2‐carbamates and related compounds as potential antifilarial agents
inferred← citeshttps://doi.org/10.1002/jhet.5570400526openalex-snapshot
Hypervalent iodine in synthesis 93. A facile synthesis of 2‐substituted imidazo[1,2‐a]pyrimidines by cyclocondensation of alkynyl(phenyl)iodonium salts and 2‐aminopyrimidine
inferred← citeshttps://doi.org/10.1002/qsar.200420045openalex-snapshot
Microwave‐assisted Synthesis of a 3‐Aminoimidazo[1,2‐a]‐pyridine/pyrazine Library by Fluorous Multicomponent Reactions and Subsequent Cross‐coupling Reactions
inferred← citeshttps://doi.org/10.1002/qua.22595openalex-snapshot
Quantum chemical studies on prototautomerism of 1H‐imidazo[4,5‐c]pyridine
inferred← citeshttps://doi.org/10.1002/slct.201601460openalex-snapshot
N‐Bromosuccinimide Promoted Direct Thiolation of Imidazoheteroaryl C‐H bonds with Disulfides
inferred← citeshttps://doi.org/10.1002/slct.201700557openalex-snapshot
Catalyst‐Free, Glycerol‐Assisted Facile Approach to Imidazole‐Fused Nitrogen‐Bridgehead Heterocycles
inferred← citeshttps://doi.org/10.1002/slct.202002219openalex-snapshot
Metal‐Free, H 2 O 2 ‐Mediated, Regioselective Direct C‐3 Hydroxylation of Imidazo[1,2‐ a ]pyridines via C(sp 2 )‐H Bond Functionalization
inferred← citeshttps://doi.org/10.1002/slct.202002894openalex-snapshot
Sustainable Synthetic Approaches for 3‐Aminoimidazo‐fused Heterocycles via Groebke‐Blackburn‐Bienaymé Process
inferred← citeshttps://doi.org/10.1002/slct.202003922openalex-snapshot
Synthesis of 2‐Chloro‐ N ‐(4‐(6‐chloro H ‐imidazo[1,2‐a]pyridin‐2‐yl)phenyl) Acetamide Derivatives as Antitubercular Agents
inferred← citeshttps://doi.org/10.1002/slct.202100682openalex-snapshot
Sulfur Catalyzed Metal‐ and Solvent‐Free ABB'C Four‐Component Synthesis of N ‐Arylidene‐2‐aryl‐imidazo[1‐2‐ a ]azin‐3‐amines via Strecker Reaction
inferred← citeshttps://doi.org/10.1002/slct.202500114openalex-snapshot
Cobalt‐Mediated Selective Synthesis of Iodine Functionalized Imidazo‐Fused Heterocycles Using 2‐Aminopyridine, Styrene or Acetophenone
inferred← citeshttps://doi.org/10.1002/tcr.201600057openalex-snapshot
Design, Synthesis, and Functionalization of Imidazoheterocycles
inferred← citeshttps://doi.org/10.1002/tcr.201600146openalex-snapshot
Synthesis of Imidazo[1,2‐a]pyridines: C‐H Functionalization in the Direction of C‐S Bond Formation
inferred← citeshttps://doi.org/10.1002/tcr.202100240openalex-snapshot
Ortho C−H Functionalization of 2‐Arylimidazo[1,2‐ a ]pyridines
inferred← citeshttps://doi.org/10.1002/vjch.202300362openalex-snapshot
Efficient synthesis and characterization of imidazo[1,2‐a]pyridine‐8‐carboxamide derivatives: A promising scaffold for drug development
inferred← citeshttps://doi.org/10.1002/zfch.19790190106openalex-snapshot
Heterocyclisch substituierte Thiazole als Thiabendazol‐Analoge
inferred← citeshttps://doi.org/10.1007/978-3-0348-7111-2_1openalex-snapshot
Chemotherapy of hookworm infections
inferred← citeshttps://doi.org/10.1007/s00044-019-02386-6openalex-snapshot
Synthesis and anti-inflammatory activity of 1,2-3-substituted 2a1,4,5-triazacyclopenta[cd]indene derivatives
inferred← citeshttps://doi.org/10.1007/s00044-020-02638-wopenalex-snapshot
Synthesis and anticancer evaluation of amide derivatives of imidazo-pyridines
inferred← citeshttps://doi.org/10.1007/s00044-022-02997-6openalex-snapshot
Synthesis and cytotoxic/antimicrobial screening of 2-alkenylimidazo[1,2-a]pyrimidines
inferred← citeshttps://doi.org/10.1007/s00706-017-1950-8openalex-snapshot
An efficient access to 2,3-diarylimidazo[1,2-a]pyridines via silver(I)-catalyzed C-H bond functionalization
inferred← citeshttps://doi.org/10.1007/s10593-019-02432-6openalex-snapshot
Synthesis of Substituted Imidazo[1,2-a]Pyridin-3-yl-Acetic Acids by Multicomponent Condensation of 2-Aminopyridines with Arylglyoxals and Meldrum’s Acid
inferred← citeshttps://doi.org/10.1007/s10822-025-00617-0openalex-snapshot
N-imidazopyridine derivatives of noscapine as potent tubulin-binding anticancer agents: chemical synthesis and cellular evaluation
inferred← citeshttps://doi.org/10.1007/s11030-016-9666-yopenalex-snapshot
$$\hbox {I}_{2}$$ I 2 -mediated amination/cyclization of ketones with 2-aminopyridines under high-speed ball milling: solvent- and metal-free synthesis of 2,3-substituted imidazo[1,2-a]pyridines and zolimidine
inferred← citeshttps://doi.org/10.1007/s11030-023-10669-9openalex-snapshot
Regioselective synthesis and molecular docking studies of functionalized imidazo [1,2-a]pyridine derivatives through MCRs
inferred← citeshttps://doi.org/10.1007/s11030-026-11578-3openalex-snapshot
Design, synthesis, anticancer estimation, and computational studies of novel benzochromenoimidazopyrimidines as CDK-2 inhibitors and apoptosis stimulators
inferred← citeshttps://doi.org/10.1007/s11164-013-1352-4openalex-snapshot
Multi-walled carbon nanotubes sulfuric acid as a reusable heterogeneous solid acid catalyst for the rapid synthesis of imidazo[1,2-a]pyridines
inferred← citeshttps://doi.org/10.1007/s11164-021-04554-zopenalex-snapshot
Survey reactivity of 2-aminopyridine and Meldrum’s acid in the presence of aryl glyoxals or aryl aldehydes; ethyl 2-(3-aryl imidazo[1,2-a]pyridin-2-yl)acetates versus ethyl 3-aryl-3-(pyridin-2-ylamino)propanoates
inferred← citeshttps://doi.org/10.1007/s11172-006-0494-6openalex-snapshot
New catalytic system for the synthesis of imidazo[1,2-a]pyridines by the Ugi reaction
inferred← citeshttps://doi.org/10.1007/s11224-009-9433-0openalex-snapshot
FT-IR spectra, vibrational assignments, and density functional calculations of imidazo[1,2-a]pyridine molecule and its Zn(II) halide complexes
inferred← citeshttps://doi.org/10.1007/s13738-023-02808-8openalex-snapshot
KI-Oxone catalyzed ultrasound-promoted synthesis of imidazo[1,2-a]-pyridine-3-carboxylates (IPCs) and evaluation of their anti-tubercular activity
inferred← citeshttps://doi.org/10.1007/s13738-026-03411-3openalex-snapshot
Novel synthetic approach for regioselective nitration of 2-arylimidazo[1,2-a]pyridines using iodobenzene diacetate and copper nitrate
inferred← citeshttps://doi.org/10.1007/s42823-023-00603-2openalex-snapshot
Design, synthesis and biological studies of tetrazole fused imidazopyridines
inferred← citeshttps://doi.org/10.1007/s44371-025-00394-7openalex-snapshot
Two step synthesis, characterization and anti-bacterial activity of series of dihydroisobenzofuran-5-yl)-5-(pyridin-2-yl)-1H-imidazol-2-yl) pyrazine/pyrimidines
inferred← citeshttps://doi.org/10.1016/0020-7519(89)90091-xopenalex-snapshot
Experimental and theoretical studies of anthelmintics: Oxfendazole and its imidazo[1,2-a]pyridine-2-carbamate isomer
inferred← citeshttps://doi.org/10.1016/0169-7439(93)80022-aopenalex-snapshot
Inhibitory effects on platelet aggregation and cyclic AMP phosphodiesterase of azaindolizine-type compounds
inferred← citeshttps://doi.org/10.1016/0223-5234(94)90057-4openalex-snapshot
Synthesis and cardiotonic activity of aryl- or pyridyl-substituted fused imidazoles
inferred← citeshttps://doi.org/10.1016/b978-0-323-91221-1.00014-2openalex-snapshot
Synthetic strategies of functionalized pyridines and their therapeutic potential as multifunctional anti-Alzheimer's agents
inferred← citeshttps://doi.org/10.1016/j.arabjc.2017.02.007openalex-snapshot
Hypervalent iodine(III) catalyzed rapid and efficient access to benzimidazoles, benzothiazoles and quinoxalines: Biological evaluation of some new benzimidazole-imidazo[1,2-a]pyridine conjugates
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106383openalex-snapshot
Imidazo[1,2-a]quinazolines as novel, potent EGFR-TK inhibitors: Design, synthesis, bioactivity evaluation, and in silico studies
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.108102openalex-snapshot
Synthesis, Characterization, and antiviral evaluation of New Chalcone-Based Imidazo[1,2-a]pyridine Derivatives: Insights from in vitro and in silico Anti-HIV studies
inferred← citeshttps://doi.org/10.1016/j.bmc.2017.07.034openalex-snapshot
Discovery of new leads against Mycobacterium tuberculosis using scaffold hopping and shape based similarity
inferred← citeshttps://doi.org/10.1016/j.bmc.2017.11.012openalex-snapshot
Discovery of imidazo[1,2-a]pyridine-based anthelmintic targeting cholinergic receptors of Haemonchus contortus
inferred← citeshttps://doi.org/10.1016/j.bmc.2022.116835openalex-snapshot
Organocatalyzed umpolung addition for synthesis of heterocyclic-fused arylidene-imidazolones as anticancer agents
inferred← citeshttps://doi.org/10.1016/j.bmc.2025.118141openalex-snapshot
A comprehensive review of fused imidazonaphthyridine derivatives: Synthetic approaches and biological applications
inferred← citeshttps://doi.org/10.1016/j.bmcl.2019.06.031openalex-snapshot
Rational design, molecular docking and synthesis of novel homopiperazine linked imidazo[1,2-a]pyrimidine derivatives as potent cytotoxic and antimicrobial agents
inferred← citeshttps://doi.org/10.1016/j.cbi.2023.110606openalex-snapshot
Rational design of novel microtubule targeting anticancer drugs N-imidazopyridine noscapinoids: Chemical synthesis and experimental evaluation based on in vitro using breast cancer cells and in vivo using xenograft mice model
inferred← citeshttps://doi.org/10.1016/j.cclet.2014.12.016openalex-snapshot
Direct one-pot synthesis of zolimidine pharmaceutical drug and imidazo[1,2-a]pyridine derivatives via I2/CuO-promoted tandem strategy
inferred← citeshttps://doi.org/10.1016/j.cdc.2023.101001openalex-snapshot
Design, synthesis and biological evaluation of amide derivatives of isoxazole-imidazo[1,2-a]pyridine as anticancer agents
inferred← citeshttps://doi.org/10.1016/j.cdc.2023.101036openalex-snapshot
Synthesis and biological evaluation of novel amide derivatives of 1,2,4-oxadiazole-imidazopyridines as anticancer agents
inferred← citeshttps://doi.org/10.1016/j.cdc.2023.101092openalex-snapshot
Synthesis and biological evaluation of tetrazole fused imidazopyridine derivatives as anticancer agents
inferred← citeshttps://doi.org/10.1016/j.chphi.2024.100494openalex-snapshot
New 2-Chloroimidazo[1,2-a]pyridine induced Schiff bases: Synthesis, characterization, antimicrobial and A-498 and A-549 anticancer activity, molecular modeling, in-silico pharmacokinetics, and DFT studies
inferred← citeshttps://doi.org/10.1016/j.chphi.2024.100694openalex-snapshot
Imidazo[1,2-a]pyridine-appended chalcone and Schiff base conjugates: Synthetic, spectrophotometric, biological, and computational aspects
inferred← citeshttps://doi.org/10.1016/j.crci.2015.10.014openalex-snapshot
Composés á structure imidazopyridinyl-arylpropénone, nouveaux agents anti-infectieux potentiels
inferred← citeshttps://doi.org/10.1016/j.dyepig.2015.05.014openalex-snapshot
CuO–CuAl2O4 and d-glucose catalyzed synthesis of a family of excited state intramolecular proton transfer imidazo[1,2-a]pyridine analogues and their optical properties
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.113048openalex-snapshot
Design, synthesis, and biodistribution studies of new analogues of marine alkaloids: Potent in vitro and in vivo fungicidal agents against Candida spp.
inferred← citeshttps://doi.org/10.1016/j.mencom.2009.05.017openalex-snapshot
Vicarious nucleophilic substitution in nitro derivatives of imidazo[1,2-a]pyridine
inferred← citeshttps://doi.org/10.1016/j.molliq.2023.121863openalex-snapshot
Solvent effect on molecular, electronic parameters, topological analysis and Fukui function evaluation with biological studies of imidazo [1, 2-a] pyridine-8-carboxylic acid
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.133921openalex-snapshot
Supramolecular co-crystal of 4-dimethyl aminopyridine with Picric acid (4DMAP: PA): Synthesis, single crystal investigation, HF/DFT inspection, Hirshfeld surface and antifungal activity
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.134238openalex-snapshot
Design, synthesis, in vitro α-glucosidase inhibitory, antioxidant activity and molecular docking studies of novel pyridine linked imidazo[1,2-a]pyridine derivatives
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.138701openalex-snapshot
Synthesis, spectroscopic characterization, crystal structure, DFT calculations, anti-cancer activities and Hirshfeld surface analysis of 2-((4-chlorophenyl)amino)-2-oxoethyl 2-ethylimidazo[1,2-a]pyridine-3-carboxylate
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.142608openalex-snapshot
Synthesis, characterization, crystal structure, Hirshfeld analysis and theoretical investigation of 8-cyano-2-ethoxycarbonylimidazo[1,2-a]pyridines
inferred← citeshttps://doi.org/10.1016/j.poly.2012.03.026openalex-snapshot
Novel trans-dioxorhenium complex with imidazo[1,2a]pyridine ligand – Synthesis, spectroscopic and electrochemical characterization, X-ray crystal structure and DFT calculations
inferred← citeshttps://doi.org/10.1016/j.rechem.2022.100474openalex-snapshot
A novel manganese/iodine-catalyzed Ortoleva-King type protocol for the synthesis of imidazo[1,2-a]pyridines and Zolimidine
inferred← citeshttps://doi.org/10.1016/j.rechem.2022.100750openalex-snapshot
Nickel/iodine-catalyzed synthesis of 2-arylimidazo[1,2-a]pyridines through Ortoleva-King type protocol
inferred← citeshttps://doi.org/10.1016/j.rechem.2023.101070openalex-snapshot
Synthesis of imidazo[1,2-a]pyridine derivatives and Zolimidine via a novel zinc/iodine-catalyzed Ortoleva-King type protocol
inferred← citeshttps://doi.org/10.1016/j.rechem.2024.101790openalex-snapshot
The synthesis of Fe3O4@SiO2-NNO-CuII nanocatalyst and investigation of its application in the synthesis of imidazo[1,2-a]pyridines
inferred← citeshttps://doi.org/10.1016/j.saa.2011.12.073openalex-snapshot
FT-IR and FT-Raman spectroscopic and DFT theoretical studies on 4-azabenzimidazole
inferred← citeshttps://doi.org/10.1016/j.tet.2011.09.120openalex-snapshot
Grignard reagent-promoted 6-endo-dig cyclization: instantaneous synthesis of original dipyrido[1,2-a:3′,4′-d]imidazole
inferred← citeshttps://doi.org/10.1016/j.tet.2014.09.067openalex-snapshot
Synthesis of 3-aroylimidazo[1,2-a]pyridines via CuCl2 catalyzed tandem dual carbon–nitrogen bonding
inferred← citeshttps://doi.org/10.1016/j.tet.2016.01.023openalex-snapshot
Synthesis of novel imidazo[1,2-a]pyridine-4-hydroxy-2H-coumarins by Groebke–Blackburn–Bienaymé multicomponent reaction as potential NS5B inhibitors
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131643openalex-snapshot
First biocatalytic Groebke-Blackburn-Bienaymé reaction to synthesize imidazo[1,2-a]pyridine derivatives using lipase enzyme
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132510openalex-snapshot
Metal-free, Tf2NH-catalyzed 1, 6-conjugate addition of imidazopyridine to para-quinone methides: Easy access to C3-functionalized triarylmethane imidazopyridine
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133809openalex-snapshot
Cu-catalysed diversity-oriented synthesis of isoxazole and imidazo[1,2-a]azine conjugates
inferred← citeshttps://doi.org/10.1016/j.tet.2026.135347openalex-snapshot
Synthesis, characterization and antifungal evaluation of benzofuran-based thiazole derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.04.008openalex-snapshot
Multicomponent synthesis of imidazo[1,2-a]pyridines using catalytic zinc chloride
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.08.090openalex-snapshot
Cu(OTf)2-catalyzed synthesis of imidazo[1,2-a]pyridines from α-diazoketones and 2-aminopyridines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.12.121openalex-snapshot
One-pot, three-component synthesis of 1-amidomethyl-imidazo[1,2-a]pyridines catalyzed by ytterbium triflate
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.04.126openalex-snapshot
Facile three-component domino reactions for the synthesis of 2-arylimidazo[1,2-a]pyridines and 2-arylimidazo[2,1-a]isoquinolines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.08.112openalex-snapshot
Water mediated deprotective intramolecular hydroamination of N-propargylaminopyridines: synthesis of imidazo[1,2-a]pyridines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.12.018openalex-snapshot
An expeditious approach to access 2-arylimidazo[1,2-a]pyridin-3-ol from 2-amino pyridine through a novel Petasis based cascade reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.12.014openalex-snapshot
Choline chloride/urea as a deep eutectic solvent/organocatalyst promoted three-component synthesis of 3-aminoimidazo-fused heterocycles via Groebke–Blackburn–Bienayme process
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.05.064openalex-snapshot
Copper-catalyzed intramolecular oxidative amination of enaminone C–H bond for the synthesis of imidazo[1,2- a ]pyridines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.11.081openalex-snapshot
Copper-catalyzed four-component synthesis of imidazo[1,2-a]pyridines via sequential reductive amination, condensation, and cyclization
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.04.075openalex-snapshot
Green synthesis of imidazo[1,2-a]pyridines using calix[6]arene-SO3H surfactant in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.02.001openalex-snapshot
Electrochemical oxidative selenylation of imidazo[1,2–a]pyridines with diselenides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.03.008openalex-snapshot
K2S2O8-Mediated halogenation of 2-arylimidazo[1,2-a]pyridines using sodium halides as the halogen sources
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.150950openalex-snapshot
Novel one step synthesis of imidazo[1,2-a]pyridines and Zolimidine via iron/iodine-catalyzed Ortoleva-King type protocol
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151590openalex-snapshot
TEMPO-mediated cross dehydrogenative coupling aminomethylation of imidazopyridine
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154295openalex-snapshot
Synthesis of 2,3-bifunctional imidazo[1,2-a]pyridines through cycloadditions of pyridinium ylides with N-cyano-4-methyl-N-phenylbenzenesulfonamide
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.155188openalex-snapshot
Synthesis of imidazo[1,2-a]pyridines via cobalt/iodine-catalyzed Ortoleva-King type approach
inferred← citeshttps://doi.org/10.1016/j.tetlet.2026.156046openalex-snapshot
Synthesis of diazadibenzo[cd,h]azulenes by combination of chemoselective cross-coupling and alkyne‑carbonyl metathesis (ACM) reactions
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)00003-4openalex-snapshot
A novel dealkylation affording 3-aminoimidazo[1,2-a]pyridines: access to new substitution patterns by solid-phase synthesis
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)76784-0openalex-snapshot
Imidazole derivatives, part IX selective reactions of functionalized imidazo[1,2-a]pyridines: stereospecific synthesis of 5,6-dihydroimidazo[1,2-a]pyridines
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)00653-4openalex-snapshot
Parallel synthesis of 3-aminoimidazo[1,2-a]pyridines and pyrazines by a new three-component condensation
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)01113-7openalex-snapshot
A three-component solid-phase synthesis of 3-aminoimidazo[1,2-a]azines
inferred← citeshttps://doi.org/10.1016/s0165-7208(97)80030-xopenalex-snapshot
Benzimidazoles
inferred← citeshttps://doi.org/10.1016/s1054-3589(08)60254-9openalex-snapshot
Experimental Approaches to Antifungal Chemotherapy
inferred← citeshttps://doi.org/10.1016/s1386-1425(99)00200-0openalex-snapshot
Effect of solvents on the photophysical properties of substituted imidazonaphthyridine derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00960openalex-snapshot
Rh-Catalyzed Twofold Conjugate Addition of 2-Arylimidazo[1,2- a ]pyridines to p -Quinols To Access Bridged Scaffolds with Three Contiguous Stereocenters
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00480openalex-snapshot
Copper-Catalyzed Oxidative Cyclization of 2-Amino-azaarenes with Lignin Models: Synthesis of 3-Phenoxy Imidazo Heterocycles
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00765openalex-snapshot
I2O5-Mediated Iodocyclization Cascade of N-(1-Arylallyl)pyridine-2-amines with Concomitant C═C Bond Cleavage: A Synthesis of 3-Iodoimidazo[1,2-a]pyridines
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01118openalex-snapshot
[4 + 2]-Annulation of MBH-Acetates of Acetylenic Aldehydes with Imidazoles/Benzimidazoles To Access Imidazo[1,2-a]pyridines/Benzimidazo[1,2-a]pyridines
inferred← citeshttps://doi.org/10.1021/acscombsci.7b00173openalex-snapshot
Efficient Access to Imidazo[1,2- a ]pyridines/pyrazines/pyrimidines via Catalyst-Free Annulation Reaction under Microwave Irradiation in Green Solvent
inferred← citeshttps://doi.org/10.1021/acsomega.0c01478openalex-snapshot
Iodine Promoted Efficient Synthesis of 2-Arylimidazo[1,2- a ]pyridines in Aqueous Media: A Comparative Study between Micellar Catalysis and an “On-Water” Platform
inferred← citeshttps://doi.org/10.1021/acsomega.0c03941openalex-snapshot
Eosin Y-Catalyzed Synthesis of 3-Aminoimidazo[1,2- a ]Pyridines via the HAT Process under Visible Light through Formation of the C–N Bond
inferred← citeshttps://doi.org/10.1021/acsomega.1c02645openalex-snapshot
Ultrasound-Assisted Iodination of Imidazo[1,2-α]pyridines Via C–H Functionalization Mediated by tert-Butyl Hydroperoxide
inferred← citeshttps://doi.org/10.1021/acsomega.3c06841openalex-snapshot
Synthesis, Characterizations, and Quantum Chemical Investigations on Imidazo[1,2-a]pyrimidine-Schiff Base Derivative: (E)-2-Phenyl-N-(thiophen-2-ylmethylene)imidazo[1,2-a]pyrimidin-3-amine
inferred← citeshttps://doi.org/10.1021/acsomega.8b03581openalex-snapshot
Efficient and “Green” Synthetic Route to Imidazo[1,2- a ]pyridine by Cu(II)–Ascorbate-Catalyzed A3-Coupling in Aqueous Micellar Media
inferred← citeshttps://doi.org/10.1021/cc900103ropenalex-snapshot
Novel One-Pot Three Component Reaction for the Synthesis of [2-(Alkylsulfanyl)imidazo[1,2-a]pyridin-3-yl](aryl)methanone
inferred← citeshttps://doi.org/10.1021/jo0012602openalex-snapshot
Efficient Syntheses of Imidazolo[1,2-a]pyridines and -[2,1-a]isoquinolines
inferred← citeshttps://doi.org/10.1021/jo0712603openalex-snapshot
Synthesis of Polysubstituted Imidazo[1,2-a]pyridines via Microwave-Assisted One-Pot Cyclization/Suzuki Coupling/Palladium-Catalyzed Heteroarylation
inferred← citeshttps://doi.org/10.1021/jo9916129openalex-snapshot
A Facile Access to 2-Methylthio/Alkoxy/Amino-3-acylimidazo[1,2-a]pyridines Based on Cupric Chloride Promoted Oxidative Ring Closure of α-Oxoketene N,S-, N,O-, and N,N-Acetals
inferred← citeshttps://doi.org/10.1021/ol401655ropenalex-snapshot
Copper-Catalyzed Tandem Azide–Alkyne Cycloaddition, Ullmann Type C–N Coupling, and Intramolecular Direct Arylation
inferred← citeshttps://doi.org/10.1021/ol501117zopenalex-snapshot
N-Chlorosuccinimide-Promoted Regioselective Sulfenylation of Imidazoheterocycles at Room Temperature
inferred← citeshttps://doi.org/10.1039/c1sc00122aopenalex-snapshot
Asymmetric organocatalytic [3 + 2]-annulation strategy for the synthesis of N-fused heteroaromatic compounds
inferred← citeshttps://doi.org/10.1039/c3ra43221aopenalex-snapshot
Facile synthesis of imidazo[1,2-a]pyridines via a one-pot three-component reaction under solvent-free mechanochemical ball-milling conditions
inferred← citeshttps://doi.org/10.1039/c3ra43889aopenalex-snapshot
Copper catalyzed tandem oxidative C–H amination/cyclizations: Direct access to imidazo[1,2-a]pyridines
inferred← citeshttps://doi.org/10.1039/c4cc08495kopenalex-snapshot
Synthesis of imidazo[1,2-a]pyridines: a decade update
inferred← citeshttps://doi.org/10.1039/c4cy00919copenalex-snapshot
Heterogeneous biomimetic aerobic synthesis of 3-iodoimidazo[1,2-a]pyridines via CuO x /OMS-2-catalyzed tandem cyclization/iodination and their late-stage functionalization
inferred← citeshttps://doi.org/10.1039/c4ra03299copenalex-snapshot
Heterogeneously copper-catalyzed oxidative synthesis of imidazo[1,2-a]pyridines using 2-aminopyridines and ketones under ligand- and additive-free conditions
inferred← citeshttps://doi.org/10.1039/c4ra13056aopenalex-snapshot
One-pot, three component tandem reaction of 2-aminopyridines, acetophenones and aldehydes: synthesis of 3-aroylimidazo[1,2-a]pyridines
inferred← citeshttps://doi.org/10.1039/c5gc02771copenalex-snapshot
One pot synthesis of substituted imidazopyridines and thiazoles from styrenes in water assisted by NBS
inferred← citeshttps://doi.org/10.1039/c5ra07770bopenalex-snapshot
Highly efficient and eco-friendly protocol to functionalized imidazoles via ring-opening of α-nitro epoxides
inferred← citeshttps://doi.org/10.1039/c5ra10891hopenalex-snapshot
Novel one-pot pseudo four component reaction: expeditious synthesis of functionalized imidazo[1,2-a]pyridines
inferred← citeshttps://doi.org/10.1039/c5ra15078gopenalex-snapshot
Palladium(0)-catalyzed direct C–H hetero-arylation of 2-arylimidazo [1,2-a]pyridines with (E)-1-(5-bromothiophen-2-yl)-3-arylprop-2-en-1-ones and their anticancer activity
inferred← citeshttps://doi.org/10.1039/c6nj02134dopenalex-snapshot
Fe–SBA-15 catalyzed synthesis of 2-alkoxyimidazo[1,2-a]pyridines and screening of their in silico selectivity and binding affinity to biological targets
inferred← citeshttps://doi.org/10.1039/c6ra12166gopenalex-snapshot
Ligand-free Pd-catalysed decarboxylative arylation of imidazo[1,2-a]pyridine-3-carboxylic acids with aryl bromides
inferred← citeshttps://doi.org/10.1039/c7ob01384aopenalex-snapshot
A facile I 2 -catalyzed synthesis of imidazo[1,2-a]pyridines via sp 3 C–H functionalization of azaarenes and evaluation of anticancer activity
inferred← citeshttps://doi.org/10.1039/c7qo00875aopenalex-snapshot
Cobalt-catalyzed cross-dehydrogenative coupling of imidazo[1,2- a ]pyridines with isochroman using molecular oxygen as the oxidant
inferred← citeshttps://doi.org/10.1039/c8gc03622eopenalex-snapshot
Electrochemically initiated intermolecular C–N formation/cyclization of ketones with 2-aminopyridines: an efficient method for the synthesis of imidazo[1,2- a ]pyridines
inferred← citeshttps://doi.org/10.1039/c8ob01486hopenalex-snapshot
Chloroform as a carbon monoxide source in palladium-catalyzed synthesis of 2-amidoimidazo[1,2- a ]pyridines
inferred← citeshttps://doi.org/10.1039/c9nj05426jopenalex-snapshot
La(OTf) 3 -catalysed one-pot synthesis of pyrazole tethered imidazo[1,2- a ]azine derivatives and evaluation of their light emitting properties
inferred← citeshttps://doi.org/10.1039/d1cc03089bopenalex-snapshot
HFIP promoted thio(hetero)arylation of imidazoheterocycles under metal- and base-free conditions
inferred← citeshttps://doi.org/10.1039/d1cc04602kopenalex-snapshot
2-Aminopyridine – an unsung hero in drug discovery
inferred← citeshttps://doi.org/10.1039/d1ob01683kopenalex-snapshot
Palladium( ii ) catalyzed site-selective C–H olefination of imidazo[1,2- a ]pyridines
inferred← citeshttps://doi.org/10.1039/d1ob01822aopenalex-snapshot
Electrochemical sulfonylation of imidazoheterocycles under batch and continuous flow conditions
inferred← citeshttps://doi.org/10.1039/d2nj06165aopenalex-snapshot
Microwave-assisted Cu( i )-catalyzed one-pot tandem synthesis of pyridoimidazole-fused quinolines as new antimycobacterial agents: DFT and ESI-HRMS study
inferred← citeshttps://doi.org/10.1039/d2ra07021aopenalex-snapshot
Silica supported lanthanum trifluoroacetate and trichloroacetate as an efficient and reusable water compatible Lewis acid catalyst for synthesis of 2,4,5-triarylimidazoles via a solvent-free green approach
inferred← citeshttps://doi.org/10.1039/d3gc04062copenalex-snapshot
Visible light-mediated copper catalyzed regioselective diamination of terminal alkynes at room temperature: a facile synthesis of substituted imidazo[1,2-α]pyridines
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/d3ra03852aopenalex-snapshot
Metal-free C-3 selective C(sp 2 )–C(sp 3 ) heteroarylation of anilines with imidazo[1,2- a ]pyridine derivatives via cross-dehydrogenative coupling
inferred← citeshttps://doi.org/10.1039/d3ra07842fopenalex-snapshot
Iodine catalyzed synthesis of imidazo[1,2- a ]pyrazine and imidazo[1,2- a ]pyridine derivatives and their anticancer activity
inferred← citeshttps://doi.org/10.1039/d4ra07561gopenalex-snapshot
Synthesis, crystal structure, and antiviral evaluation of new imidazopyridine-schiff base derivatives: in vitro and in silico anti-HIV studies
inferred← citeshttps://doi.org/10.1055/a-2348-4764openalex-snapshot
Oxidative Cross-Dehydrogenative C–H Bond Amination of Imidazo[1,2-a]pyridines in Aqueous Media under Metal-Free Conditions
inferred← citeshttps://doi.org/10.1055/a-2695-8185openalex-snapshot
Cu(acac)2-Catalyzed A3-(Aldehyde-amine-alkyne) Coupling Reaction for the Synthesis of a Wide Range of Propargylamines and Entry to Imidazo[1,2-a]pyridines
inferred← citeshttps://doi.org/10.1055/s-0036-1558965openalex-snapshot
Application of Triphenylammonium Tricyanomethanide as an Efficient and Recyclable Nanostructured Molten-Salt Catalyst for the Synthesis of N-Benzylidene-2-arylimidazo[1,2-a]pyridin-3-amines
inferred← citeshttps://doi.org/10.1071/ch14119openalex-snapshot
Synthesis of Heterocyclic-fused Imidazoles by Pyrolysis of N-Heterocyclic Isoxazol-5(2H)-ones
inferred← citeshttps://doi.org/10.1080/00304948.2011.564558openalex-snapshot
An Efficient Synthesis of Zolpidem
inferred← citeshttps://doi.org/10.1080/00397911.2019.1691738openalex-snapshot
Visible light-mediated photocatalytic bromination of 2-arylimidazo[1,2-a]pyridines using CBr4 as bromine source
inferred← citeshttps://doi.org/10.1080/00397911.2020.1803915openalex-snapshot
Advancements in chemical methodologies for the synthesis of 3-aroylimidazo[1,2-a]pyridines: an update of the decade
inferred← citeshttps://doi.org/10.1080/00397911.2022.2069506openalex-snapshot
Sulfonyl hydrazide induced sulfenylation of imidazoheteroarenes: A ‘catalyst and solvent free’ protocol
inferred← citeshttps://doi.org/10.1080/00397911.2023.2191205openalex-snapshot
One-pot synthesis of a new series of 2-phenylimidazo[1,2-a]pyridine-3-yl derivatives
inferred← citeshttps://doi.org/10.1080/10406638.2021.1933107openalex-snapshot
Design, Synthesis, Antimicrobial and Ergosterol Inhibition Activity of New 4-(Imidazo[1,2-a]Pyridin-2-yl)Quinoline Derivatives
inferred← citeshttps://doi.org/10.1081/scc-120027273openalex-snapshot
Hypervalent Iodine in Synthesis. 94. A Facile Synthesis of 2-Substituted-imidazo[1,2-a]pyridines by Cyclocondensation of Alkynyl(phenyl) iodonium Salts and 2-Aminopyridine
inferred← citeshttps://doi.org/10.1088/1742-6596/2063/1/012016openalex-snapshot
Synthesis, spectroscopic, and thermal studies of azo compounds from luminol and procaine with acetylacetone and their complexes
inferred← citeshttps://doi.org/10.1088/1742-6596/2063/1/012024openalex-snapshot
Preparation, analytical Studies and application of a New Azodye Derived from Pharmaceutical Materials (Procaine Hydrochloride & Salicylic acid)
inferred← citeshttps://doi.org/10.1107/s1600536811003928openalex-snapshot
2-Methyl-6-(trifluoromethyl)imidazo[1,2-a]pyridine-3-carbonitrile
inferred← citeshttps://doi.org/10.1107/s160053681200685xopenalex-snapshot
2-(8-Bromoimidazo[1,2-a]pyridin-2-yl)-N′-[(E)-4-diethylamino-2-hydroxybenzylidene]acetohydrazide dihydrate
inferred← citeshttps://doi.org/10.1107/s2053229625006965openalex-snapshot
Synthesis and crystal structures of two cocrystals of imidazo[1,2- a ]pyridine-3-carbonitrile with nitro-substituted benzoic acid and phenol
inferred← citeshttps://doi.org/10.1134/s0022476618050025openalex-snapshot
Experimental and Theoretical Study on New Zn(II) Halide Complexes of 3,5-Diazaindole
inferred← citeshttps://doi.org/10.1134/s1070363224120065openalex-snapshot
Synthesis of 5,6-Dialkyl-4-aryl-2-aminopyridine-3-carbonitriles and In Vitro Study of Their Antimicrobial Activity
inferred← citeshttps://doi.org/10.1134/s1070428023070102openalex-snapshot
Silica-Zinc Chloride (SiO2-ZnCl2)-Mediated Facile Synthesis of Some Nitro-Substituted Arylimidazopyridine Analogs
inferred← citeshttps://doi.org/10.1134/s1070428023130031openalex-snapshot
Heterocyclization Reactions of Imidazo[1,2-a]pyrimidine Analogues (A Review)
inferred← citeshttps://doi.org/10.1134/s1070428025603838openalex-snapshot
Efficient, Safe, and Scalable One-Pot Telescopic Synthesis of 2-Arylimidazo[1,2-a]pyridines
showing the first 200 of 225 · page through all 225
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.