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Recent Progress in Metal-Free Direct Synthesis of Imidazo[1,2- a ]pyridines

https://doi.org/10.1021/acsomega.1c03476

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

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Regioselective C3–H Alkylation of Imidazopyridines with Donor–Acceptor Cyclopropanes

inferred← citeshttps://doi.org/10.1021/acs.joc.4c00881openalex-snapshot

Electro- and Mechanochemical Strategy as a Dual Synthetic Approach for Biologically Relevant 3-Nitro-imidazo-[1,2- a ]pyridines

inferred← citeshttps://doi.org/10.1021/acs.joc.5c01427openalex-snapshot

Substrate-Directed Annulative-Sulfonylation/Desulfonylation Cascade Using ( E )-β-Iodovinyl Sulfones: A Diverse Approach for the Synthesis of Imidazo[1,2- a ]pyridines with Sulfone Motifs

inferred← citeshttps://doi.org/10.1021/acs.macromol.2c01136openalex-snapshot

Multicomponent Polymerizations of Isocyanides, Aldehydes, and 2-Aminopyridine toward Imidazo[1,2-a]pyridine-Containing Fused Heterocyclic Polymers

inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00547openalex-snapshot

Programmed Heterocycle Synthesis Using Halomucononitriles as Pyridinimine Precursors

inferred← citeshttps://doi.org/10.1021/acsomega.3c05338openalex-snapshot

Urea Hydrogen Peroxide and Ethyl Lactate, an Eco-Friendly Combo System in the Direct C(sp2)–H Bond Selenylation of Imidazo[2,1-b]thiazole and Related Structures

inferred← citeshttps://doi.org/10.1021/acsomega.5c08365openalex-snapshot

Imidazo[1,2- a ]pyridines in Medicinal Chemistry: Recent Advances in Synthesis and Biological Activities

inferred← citeshttps://doi.org/10.1021/acsorginorgau.5c00049openalex-snapshot

Solvents’ and Reagents’ Noninnocent Roles in the Groebke–Blackburn–Bienaymé (GBB) Multicomponent Reaction: Experimental and Computational Evidence

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/d4md00059eopenalex-snapshot

Design, synthesis, molecular docking and anti-proliferative activity of novel phenothiazine containing imidazo[1,2- a ]pyridine derivatives against MARK4 protein

inferred← citeshttps://doi.org/10.1039/d4ra05198jopenalex-snapshot

FeBr 3 -catalysed synthesis of 3-aroylimidazo[1,2- a ]pyridine and 3,3′-(arylmethylene)bis(2-phenylimidazo[1,2- a ]pyridines) derivatives from 2-arylimidazo[1,2- a ]pyridines and aromatic aldehydes: an investigation about mechanistic insights

inferred← citeshttps://doi.org/10.1039/d5nj02726hopenalex-snapshot

A sustainable approach to the synthesis of 2-arylimidazo[1,2- a ]pyridines followed by sequential amino and bromo functionalization

inferred← citeshttps://doi.org/10.1039/d5ob01293gopenalex-snapshot

Cetrimide-based DES-mediated synthesis of quinoline-appended imidazo[1,2- a ]pyridines and their computational and biological studies

inferred← citeshttps://doi.org/10.1039/d5ra06789hopenalex-snapshot

One-pot CuI/ l -proline-catalysed multicomponent synthesis of pyrido[2′,1′:2,3]imidazo[4,5- c ]quinoline derivatives from 2-(2-bromophenyl)imidazo[1,2- a ]pyridines, NH 3 and DMSO under air

inferred← citeshttps://doi.org/10.1039/d5tc01128kopenalex-snapshot

Balancing the molecular twist and conformational rigidity in imidazo[1,2- a ]pyridines to achieve dual-state emissive (DSE) luminogens for applications in OLEDs and cell-imaging

inferred← citeshttps://doi.org/10.1039/d6ob00033aopenalex-snapshot

One-pot three-component synthesis of hydroxyacetylated imidazo[1,2- a ]pyridines via visible-light-mediated halogen atom transfer

inferred← citeshttps://doi.org/10.1039/d6ob00273kopenalex-snapshot

Electrochemical regioselective C-3 amination of imidazo[1,2- a ]pyridines with electron-deficient sulfonimides

inferred← citeshttps://doi.org/10.1039/d6ra03865dopenalex-snapshot

Synthesis of 5-[3-amino-imidazo[1,2- a ]pyridin-6-yl]pyridin-2-ones and derivatives through the combination of palladium-catalyzed cross-coupling and GBB multi-component reactions

inferred← citeshttps://doi.org/10.1080/00397911.2022.2056057openalex-snapshot

Synthetic strategies in development of 3-aroylimidazo[1,2-a]pyridines and 2-aroylimidazo[1,2-a]pyridines: A decade update

inferred← citeshttps://doi.org/10.1080/00397911.2023.2297957openalex-snapshot

Montmorillonite K10 clay accelerated green protocol for the pseudo-five-component synthesis of substituted imidazo[1,2-a]pyridines

inferred← citeshttps://doi.org/10.1107/s241431462500553xopenalex-snapshot

3-(4-Fluorophenyl)imidazo[1,2- a ]pyridine-2-carbaldehyde

inferred← citeshttps://doi.org/10.1126/sciadv.adr6135openalex-snapshot

Atroposelective synthesis of axially chiral imidazo[1,2- a ]pyridines via asymmetric multicomponent reaction

inferred← citeshttps://doi.org/10.1134/s1068162024050236openalex-snapshot

Synthesis of Some Novel (E)-1,5-Dimethyl-2-phenyl-4-(((2-arylimidazo[1,2-a]pyridin-3-yl)-methylene)amino)-1,2-dihydro-3H-pyrazol-3-one Derivatives: Exploring Their Antimicrobial Activity

inferred← citeshttps://doi.org/10.1134/s1070428024060204openalex-snapshot

Quaternization of Ethyl Pyridin-2-ylcarbamate with Phenacyl Bromides

inferred← citeshttps://doi.org/10.21203/rs.3.rs-6185117/v1openalex-snapshot

Leveraging In-silico Methods for Laryngeal Cancer Drug Discovery Utilizing QSAR, ligand-base Design, Molecular Docking, and Pharmacokinetic Profiling Approaches.

inferred← citeshttps://doi.org/10.2174/0113852728257006230921091216openalex-snapshot

Sustainable Synthesis of Phenazines: A Review of Green Approaches

inferred← citeshttps://doi.org/10.2174/0113852728269243231206044929openalex-snapshot

Efficient Synthesis and Characterization of 6-substituted-N-p-tolyl-imidazo[1,2- a]pyridine-8-carboxamide: A Promising Scaffold for Drug Development

inferred← citeshttps://doi.org/10.2174/0113852728367154250617095504openalex-snapshot

Exploring Synthesis and Functionalization of Imidazo[1,2˗a]pyridines: A Promising Heterocyclic Framework

inferred← citeshttps://doi.org/10.2174/0118715265274067240223040333openalex-snapshot

Imidazo[1,2-A]Pyridine: Potent Biological Activity, SAR and Docking Investigations (2017-2022)

inferred← citeshttps://doi.org/10.2174/1385272827666230123124441openalex-snapshot

An Update on the Recent Green Synthetic Approaches for Imidazo[1,2-a] Pyridine: A Privileged Scaffold

inferred← citeshttps://doi.org/10.29130/dubited.1552103openalex-snapshot

DFT studies of 2-oxo-2-phenylethyl 3-nitroso-2-phenylimidazo[1,2-a]pyridine-8-carboxylate compound

inferred← citeshttps://doi.org/10.3390/ani14030386openalex-snapshot

A New Benzo[6,7]oxepino[3,2-b] Pyridine Derivative Induces Apoptosis in Canine Mammary Cancer Cell Lines

inferred← citeshttps://doi.org/10.3390/catal15100970openalex-snapshot

Calcium Oxide Nanoparticles as Green Nanocatalysts in Multicomponent Heterocyclic Synthesis: Mechanisms, Metrics, and Future Directions

inferred← citeshttps://doi.org/10.3390/molecules27113461openalex-snapshot

Recent Developments in the Photochemical Synthesis of Functionalized Imidazopyridines

inferred← citeshttps://doi.org/10.3390/molecules29112668openalex-snapshot

Imidazopyridine Family: Versatile and Promising Heterocyclic Skeletons for Different Applications

inferred← citeshttps://doi.org/10.3390/molecules29215048openalex-snapshot

Synthesis of 6- or 8-Carboxamido Derivatives of Imidazo[1,2-a]pyridines via a Heterogeneous Catalytic Aminocarbonylation Reaction

inferred← citeshttps://doi.org/10.3762/bjoc.22.58openalex-snapshot

Preparation of 3-(alkylamino)imidazo[1,2- a ]pyridine-2-carbaldehydes via Kornblum oxidation and unexpected ring-opening reactions of the corresponding alcohols under oxidative conditions

inferred← citeshttps://doi.org/10.4018/979-8-3693-7267-8.ch011openalex-snapshot

Imidazo-Pyridines

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