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Diversification of the Three-Component Coupling of 2-Aminoheterocycles, Aldehydes, and Isonitriles: Efficient Parallel Synthesis of a Diverse and Druglike Library of Imidazo- and Tetrahydroimidazo[1,2-a] Heterocycles
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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A New Heterocyclic Multicomponent Reaction For the Combinatorial Synthesis of Fused 3-Aminoimidazoles
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Multicomponent Reactions with Isocyanides
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An Easy and Fast Conversion of N2‐[(tert‐Butoxy)carbonyl]‐ L ‐amino Acids to Corresponding Amino‐aldehydes
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Mannich reactions of heterocycles with dimethyl(methylene) ammonium chloride: A high yield, one‐step conversion of estazolam to adinazolam
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Pyrrolization processes of vinyl substituted imidazo[1,2‐a]pyridine, pyrimidine and 1,8‐naphthyridine
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N-methoxy-N-methylamides (Weinreb amides) in modern organic synthesis
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Use of a convertible isocyanide for generation of Ugi reaction derivatives on solid support: Synthesis of α-acylaminoesters and pyrroles
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Characterization of the physico-chemical properties of the imidazopyridine derivative Alpidem. Comparison with Zolpidem
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Integrating cheminformatic analysis in combinatorial chemistry
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A novel dealkylation affording 3-aminoimidazo[1,2-a]pyridines: access to new substitution patterns by solid-phase synthesis
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Y(OTf)3-catalyzed novel Mannich reaction of N-alkoxycarbonylpyrroles, formaldehyde and primary amine hydrochlorides
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N-methoxy-n-methylamides as effective acylating agents
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Parallel synthesis of 3-aminoimidazo[1,2-a]pyridines and pyrazines by a new three-component condensation
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Remarkable three-step-one-pot solution phase preparation of novel imidazolines utilizing a UDC (Ugi/de-Boc/cyclize) strategy
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Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
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Synthesis and antiviral activity of imidazo[1,2-a]pyridines
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α-Ketoamides, α-ketoesters and α-diketones as HCV NS3 protease inhibitors
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Azaindole derivatives with high affinity for the dopamine D4 receptor: Synthesis, ligand binding studies and comparison of molecular electrostatic potential maps
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Multiple-Component Condensation Strategies for Combinatorial Library Synthesis
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Polymer-Supported Tetrafluorophenol: A New Activated Resin for Chemical Library Synthesis
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UPS on Weinreb Resin: A Facile Solid-Phase Route to Aldehyde and Ketone Derivatives of “Unnatural” Amino Acids and Peptides
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Domino Reactions in Organic Synthesis
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Synthesis and hypoglycemic activity of substituted 8-(1-piperazinyl)imidazo[1,2-a]pyrazines
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Antiulcer agents. 5. Inhibition of gastric H+/K+-ATPase by substituted imidazo[1,2-a]pyridines and related analogs and its implication in modeling the high affinity potassium ion binding site of the gastric proton pump enzyme
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Antiulcer agents. 1. Gastric antisecretory and cytoprotective properties of substituted imidazo[1,2-a]pyridines
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Synthesis of imidazo[1,2-a]pyrazine derivatives with uterine-relaxing, antibronchospastic, and cardiac-stimulating properties
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Angiotensin-converting enzyme inhibitors: synthesis and biological activity of acyltripeptide analogs of enalapril
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2-Amino-3-substituted-6-[(E)-1-phenyl-2-(N-methylcarbamoyl)vinyl]imidazo[1,2-a]pyridines as a Novel Class of Inhibitors of Human Rhinovirus: Stereospecific Synthesis and Antiviral Activity
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2-Amino-4-benzyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridines: Novel Selective β3-Adrenoceptor Agonists
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Novel 2-Phenylimidazo[1,2-a]pyridine Derivatives as Potent and Selective Ligands for Peripheral Benzodiazepine Receptors: Synthesis, Binding Affinity, and in Vivo Studies
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Redox-photosensitized reactions. 10. Formation of a novel type of adduct between an NADH model and carbonyl compounds by photosensitization using Ru(bpy)32+
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Selective reductions. XVIII. Fast reaction of primary, secondary, and tertiary amides with diborane. Simple, convenient procedure for the conversion of amides to the corresponding amines
inferredcites →https://doi.org/10.1021/jo01018a071openalex-snapshot
Preparation and New Reactions of Imidazo[1,2-a]pyridines
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A Mild and Efficient Alternative to the Classical Swern Oxidation
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Stereocontrolled Synthesis of 5-Acyl-3,4-dihydro-2H-pyrroles and Related Heterocycles via Intramolecular 2-Propylidene-1,3-bis(silane)−Acylnitrilium Ion Cyclizations
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Synthesis of 2,5-Disubstituted Pyrroles and Pyrrolidines by Intramolecular Cyclization of 6-Amino-3-keto Sulfones
inferredcites →https://doi.org/10.1055/s-2002-31969openalex-snapshot
Reduction of Ethanethiol Esters to Aldehydes
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Substituent Effects on Fluorescent Properties of Imidazo[1,2- a ]pyridine-Based Compounds
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Synthesis and Antibacterial Activity of Some Imidazo(1,2-a)pyrimidine Derivatives.
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Studies on New Platelet Aggregation Inhibitors 1. Synthesis of 7-Nitro-3,4-dihydroquinoline-2(1H)-one Derivatives.
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Examination of the Computed Molecular Properties of Compounds Selected for Clinical Development
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Straightforward Bienaymé and copper catalyzed N-arylation sequence to access diverse 5H-pyrido[2′,1′:2,3]imidazo[4,5-b]indoles and analogues
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Poorly reactive 5-piperazin-1-yl-1,3,4-thiadiazol-2-amines rendered as valid substrates for Groebke–Blackburn type multi-component reaction with aldehydes and isocyanides using TMSCl as a promoter
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Greater variety in Groebke–Blackburn type 3-arylaminoimidazo[1,2-a]azines accessed via Pd-catalyzed arylation of a primary amine precursor
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tert-Butyl isocyanide revisited as a convertible reagent in the Groebke–Blackburn reaction
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Comprehensive Survey of Chemical Libraries for Drug Discovery and Chemical Biology: 2007
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Imidazolopiperazines: Hit to Lead Optimization of New Antimalarial Agents
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Development of the Large-Scale Preparation of 2-(Methanesulfonyl)benzenesulfonyl Chloride
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