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CuBr catalyzed aerobic oxidative coupling of 2-aminopyridines with cinnamaldehydes: direct access to 3-formyl-2-phenyl-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/(sici)1521-3773(19991004)38:19<2852::aid-anie2852>3.0.co;2-zopenalex-snapshot
Sleep and Its Modulation by Drugs That Affect GABAA Receptor Function
inferredcites →https://doi.org/10.1002/adsc.201300900openalex-snapshot
Copper(II)‐Catalyzed Aerobic Oxidative Coupling between Chalcone and 2‐Aminopyridine via CH Amination: An Expedient Synthesis of 3‐Aroylimidazo[1,2‐a]pyridines
inferredcites →https://doi.org/10.1002/anie.201100362openalex-snapshot
Copper‐Catalyzed Intramolecular Dehydrogenative Aminooxygenation: Direct Access to Formyl‐Substituted Aromatic N‐Heterocycles
inferredcites →https://doi.org/10.1002/cmdc.201300308openalex-snapshot
Synthesis and Biological Evaluation of Imidazopyridine–Oxindole Conjugates as Microtubule‐Targeting Agents
inferredcites →https://doi.org/10.1002/ejoc.201201258openalex-snapshot
Silver‐Catalyzed Cyclization of N‐(Prop‐2‐yn‐1‐yl)pyridin‐2‐amines
inferredcites →https://doi.org/10.1016/j.bmcl.2013.03.086openalex-snapshot
Facile synthesis of new imidazo[1,2-a]pyridines carrying 1,2,3-triazoles via click chemistry and their antiepileptic studies
inferredcites →https://doi.org/10.1016/j.cclet.2013.05.030openalex-snapshot
Synthesis and antiepileptic studies of new imidazo[1,2-a]pyridine derivatives
inferredcites →https://doi.org/10.1016/j.neulet.2014.08.036openalex-snapshot
Biological evaluation of the radioiodinated imidazo[1,2-a]pyridine derivative DRK092 for amyloid-β imaging in mouse model of Alzheimer's disease
inferredcites →https://doi.org/10.1021/np040106yopenalex-snapshot
The Role of Natural Product Chemistry in Drug Discovery
inferredcites →https://doi.org/10.1021/op9000675openalex-snapshot
Kilogram-Scale Synthesis of the CXCR4 Antagonist GSK812397
inferredcites →https://doi.org/10.1039/c0md00116copenalex-snapshot
Design, synthesis and biological evaluation of imidazopyridine/pyrimidine-chalcone derivatives as potential anticancer agents
inferredcites →https://doi.org/10.1039/c4cc08495kopenalex-snapshot
Synthesis of imidazo[1,2-a]pyridines: a decade update
inferredcites →https://doi.org/10.1039/c4cc09134eopenalex-snapshot
Cu-Catalyzed selective C3-formylation of imidazo[1,2-a]pyridine C–H bonds with DMSO using molecular oxygen
inferredcites →https://doi.org/10.2165/00023210-200519010-00008openalex-snapshot
Zolpidem
inferredcites →https://doi.org/10.2174/138955707781662645openalex-snapshot
Recent Progress in the Pharmacology of Imidazo[1,2-a]pyridines
inferredcites →https://doi.org/10.2967/jnumed.114.146944openalex-snapshot
In Vivo SPECT Imaging of Amyloid-β Deposition with Radioiodinated Imidazo[1,2-a]Pyridine Derivative DRM106 in a Mouse Model of Alzheimer's Disease

What points at this work

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inferred← citeshttps://doi.org/10.2139/ssrn.4671052openalex-extracted
inferred← citeshttps://doi.org/10.1002/9781118686263.ch13openalex-snapshot
Bicyclic Pyridines Containing Ring‐Junction Nitrogen
inferred← citeshttps://doi.org/10.1002/adsc.202000970openalex-snapshot
Application of Conjugated Carbonyls in the Synthesis of Heterocycles via Oxidative Cycloaddition and Cyclization Reactions
inferred← citeshttps://doi.org/10.1002/adsc.202400473openalex-snapshot
Iodine Mediated Annulation of Triethylamine, Aldehydes and 2‐Aminopyridines for the Synthesis of 3‐Formyl‐Imidazo [1,2‐a]pyridine Derivatives
inferred← citeshttps://doi.org/10.1002/ajoc.201600120openalex-snapshot
Metal‐Free Aminooxygenation of Alkynes: Efficient Synthesis of 3‐Aroylimidazo[1,2‐ a ]‐ N ‐Heterocycles
inferred← citeshttps://doi.org/10.1002/ajoc.202000637openalex-snapshot
In/Cu Catalyzed Multiple C−N/C−C Bond Formation via Multiple Bond Cleavage in a Three Component Synthesis of Arylimidazopyridine Carboxylates
inferred← citeshttps://doi.org/10.1002/chin.201549161openalex-snapshot
ChemInform Abstract: CuBr Catalyzed Aerobic Oxidative Coupling of 2‐Aminopyridines with Cinnamaldehydes: Direct Access to 3‐Formyl‐2‐phenyl‐imidazo[1,2‐a]pyridines.
inferred← citeshttps://doi.org/10.1002/ejoc.201601586openalex-snapshot
Switching of Regioselectivity in a Perfluorohexyl Iodide Mediated Synthesis of Phenylimidazo[1,2‐a]pyridines
inferred← citeshttps://doi.org/10.1002/ejoc.201900279openalex-snapshot
Metal‐Free Approach to Zolpidem, Alpidem and their Analogues via Amination of Dibromoalkenes Derived from Imidazopyridine and Imidazothiazole
inferred← citeshttps://doi.org/10.1002/jhet.3571openalex-snapshot
Synthesis of 4‐Hydroxy‐3‐(2‐arylimidazo[1,2‐a]pyridin‐3‐yl)quinolin‐2(1H)‐ones in the Presence of DABCO as an Efficient Organocatalyst
inferred← citeshttps://doi.org/10.1002/jhet.3746openalex-snapshot
Synthesis of imidazo[1, 2‐a]pyridines via the silver acetate‐catalyzed Groebke‐Blackburn‐Bienayme reaction with ethylene glycol as a biodegradable and sustainable solvent
inferred← citeshttps://doi.org/10.1002/slct.201601294openalex-snapshot
Synthesis of 2‐Carbonylimidazo[1,2‐ a ]pyridines via Iodine–mediated Intramolecular Cyclization of 2‐Amino‐ N ‐propargylpyridinium Bromides
inferred← citeshttps://doi.org/10.1016/b978-0-08-100755-6.00012-0openalex-snapshot
Six-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-818655-8.00140-2openalex-snapshot
Imidazoles
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.136186openalex-snapshot
Synthesis of new set of imidazo[1,2-a]pyridine-schiff bases derivatives as potential antimicrobial agents: Experimental and theoretical approaches
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00138openalex-snapshot
Discovery of Quinazolin-4(3H)-ones as NLRP3 Inflammasome Inhibitors: Computational Design, Metal-Free Synthesis, and in Vitro Biological Evaluation
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00578openalex-snapshot
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
inferred← citeshttps://doi.org/10.1038/s41598-026-62643-8openalex-snapshot
Development of new imidazopyridine-based chalcones hybrids as potent antidiabetic and antioxidant agents: synthesis, in silico and in vitro evaluation
inferred← citeshttps://doi.org/10.1039/c5cc08498aopenalex-snapshot
Metal-free oxidative cyclization of acetophenones with diamines: a facile access to phenylpyridines
inferred← citeshttps://doi.org/10.1039/c5qo00285kopenalex-snapshot
Copper-catalyzed oxidative coupling reaction of α,β-unsaturated aldehydes with amidines: synthesis of 1,2,4-trisubstituted-1H-imidazole-5-carbaldehydes
inferred← citeshttps://doi.org/10.1039/c8ob00532jopenalex-snapshot
Visible light induced tetramethylethylenediamine assisted formylation of imidazopyridines
inferred← citeshttps://doi.org/10.1039/d3ob00695fopenalex-snapshot
Annulation of α-bromocinnamaldehydes to access 3-formyl-imidazo[1,2- α ]pyridines and pyrimidines under transition metal-free conditions
inferred← citeshttps://doi.org/10.1039/d5qo01432hopenalex-snapshot
I 2 /DMSO-enabled cascade Michael addition/oxidative cyclization: access to imidazo[2,1- b ][1,3,4]thiadiazoles
inferred← citeshttps://doi.org/10.1080/10406638.2022.2154369openalex-snapshot
Highly Efficient Microwave-Assisted Synthesis of 2-Arylimidazo[1,2-a]Pyridine-3-Carbaldehydes in PEG-400
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/10.24820/ark.5550190.p010.843openalex-snapshot
Synthesis of heterocycles via aerobic oxidation
inferred← citeshttps://doi.org/10.3762/bjoc.15.165openalex-snapshot
Recent advances on the transition-metal-catalyzed synthesis of imidazopyridines: an updated coverage
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