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Six-Component Reactions for the Stereoselective Synthesis of 3-Arylidene-2-oxindoles via Sequential One-Pot Ugi/Heck Carbocyclization/Sonogashira/Nucleophilic Addition
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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 Novel Palladium-Catalyzed Domino Tsuji−Trost−Heck Process for the Synthesis of Tetrahydroanthracenes
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Multicomponent Reactions with Isocyanides
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Domino Reactions in Organic Synthesis
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Metal‐Catalyzed Cross‐Coupling Reactions
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Stereoselective Synthesis of 3‐Alkylideneoxindoles using Tandem Indium‐Mediated Carbometallation and Palladium‐Catalyzed Cross‐Coupling Reactions
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A Domino Sequence Consisting of Insertion, Coupling, Isomerization, and Diels–Alder Steps Yields Highly Fluorescent Spirocycles
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Oxindole Synthesis through Intramolecular Nucleophilic Addition of Vinylpalladiums to Aryl Isocyanates
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Palladium‐Catalyzed Three‐Component Synthesis of 3‐(Diarylmethylene)oxindoles through a Domino Sonagashira/Carbopalladation/CH Activation/CC Bond‐Forming Sequence
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Pyrrolidinyl‐Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents
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Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids
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Rhodium-catalyzed carbonylation of 2-alkynylaniline: Syntheses of 1,3-dihydroindol-2-ones
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Tandem Heck–Suzuki–Miyaura reaction: Application to the synthesis of constrained analogues of combretastatin A-4
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Palladium-catalyzed domino N-arylation/carbopalladation/C–H functionalization: three-component synthesis of 3-(diarylmethylene)oxindoles
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Synthesis of oxindoles by radical cyclisation
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Solution-Phase Parallel Synthesis of 3,5,6-Substituted Indolin-2-ones
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Recent Developments in Isocyanide Based Multicomponent Reactions in Applied Chemistry
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Asymmetric Transition Metal-Catalyzed Allylic Alkylations
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Domino Reactions in Organic Synthesis
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Oxindole-Based Inhibitors of Cyclin-Dependent Kinase 2 (CDK2): Design, Synthesis, Enzymatic Activities, and X-ray Crystallographic Analysis
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Antitumor Activity of Substituted E-3-(3,4,5-Trimethoxybenzylidene)-1,3-dihydroindol-2-ones
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Molecular Recognition of Protein Kinase Binding Pockets for Design of Potent and Selective Kinase Inhibitors
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Gini Coefficient: A New Way To Express Selectivity of Kinase Inhibitors against a Family of Kinases
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Synthesis and Biological Evaluations of 3-Substituted Indolin-2-ones: A Novel Class of Tyrosine Kinase Inhibitors That Exhibit Selectivity toward Particular Receptor Tyrosine Kinases
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DoMCoSAR: A Novel Approach for Establishing the Docking Mode That Is Consistent with the Structure−Activity Relationship. Application to HIV-1 Protease Inhibitors and VEGF Receptor Tyrosine Kinase Inhibitors
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Identification of Substituted 3-[(4,5,6,7-Tetrahydro-1H-indol-2-yl)methylene]- 1,3-dihydroindol-2-ones as Growth Factor Receptor Inhibitors for VEGF-R2 (Flk-1/KDR), FGF-R1, and PDGF-Rβ Tyrosine Kinases
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A Tandem Heck-Carbocyclization/Suzuki-Coupling Approach to the Stereoselective Syntheses of Asymmetric 3,3-(Diarylmethylene)indolinones
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Stereoselective Synthesis of 3-Alkylideneoxindoles via Palladium-Catalyzed Domino Reactions
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Electrophilic ipso -Iodocyclization of N -(4-Methylphenyl)propiolamides: Selective Synthesis of 8-Methyleneazaspiro[4,5]trienes
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Palladium-Catalyzed C−H Functionalization of N-Arylpropiolamides with Aryliodonium Salts: Selective Synthesis of 3-(1-Arylmethylene)oxindoles
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Ugi-Post Functionalization, from a Single Set of Ugi-Adducts to Two Distinct Heterocycles by Microwave-Assisted Palladium-Catalyzed Cyclizations: Tuning the Reaction Pathways by Ligand Switch
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One-Pot Homolytic Aromatic Substitutions/HWE Olefinations under Microwave Conditions for the Formation of a Small Oxindole Library
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Stereoselective Synthesis of 3-Alkylideneoxindoles Using Tandem In-Mediated Carbometalation and Pd-Catalyzed Cross-Coupling Reaction
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Rhodium-Catalyzed Multicomponent-Coupling Reactions Involving a Carborhodation−Cross-Coupling Sequence
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Synthesis of 3-(Diarylmethylenyl)oxindole by a Palladium-Catalyzed Domino Carbopalladation/C−H Activation/C−C Bond-Forming Process
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Stereoselective Synthesis of 3-Alkylideneoxindoles by Rhodium-Catalyzed Cyclization Reaction of 2-Alkynylaryl Isocyanates with Aryl- and Alkenylboronic Acids
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Rhodium-Catalyzed Borylative Cyclization of 2-Alkynylaryl Isocyanates with Bis(pinacolato)diboron
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Synthesis of (2-Oxoindolin-3-ylidene)methyl Acetates Involving a C−H Functionalization Process
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Heterobimetallic Cobalt/Rhodium Nanoparticle-Catalyzed Carbonylative Cycloaddition of 2-Alkynylanilines to Oxindoles
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Stereoselective Oxindole Synthesis by Palladium-Catalyzed Cyclization Reaction of 2-(Alkynyl)aryl Isocyanates with Amides
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Iron Trichloride-Promoted Cyclization of o-Alkynylaryl Isocyanates: Synthesis of 3-(Chloromethylene)oxindoles
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Novel synthesis of oxindoles from carbamoyl chlorides via palladium catalysed cyclisation–anion capture
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Synthesis of 3-Arylideneindolin-2-ones from 2-Aminophenols by Ugi Four-Component Reaction and Heck Carbocyclization
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Asymmetric Syntheses of Oxindole and Indole Spirocyclic Alkaloid Natural Products
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The small molecule Hesperadin reveals a role for Aurora B in correcting kinetochore–microtubule attachment and in maintaining the spindle assembly checkpoint
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Protein Kinase Inhibitors: Insights into Drug Design from Structure
inferredcites →https://doi.org/10.1126/science.276.5314.955openalex-snapshot
Structures of the Tyrosine Kinase Domain of Fibroblast Growth Factor Receptor in Complex with Inhibitors
inferredcites →https://doi.org/10.2147/tcrm.2007.3.2.341openalex-snapshot
Sunitinib: a novel tyrosine kinase inhibitor. A brief review of its therapeutic potential in the treatment of renal carcinoma and gastrointestinal stromal tumors (GIST)
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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A copper-based catalytic system for carboxylation of terminal alkynes: synthesis of alkyl 2-alkynoates
inferred← citeshttps://doi.org/10.1039/c2ra22355dopenalex-snapshot
A highly efficient ultrasound-promoted synthesis of 2,3-disubstituted benzo[b]furans via intramolecular C–C bond formation in ionic liquid[bmim]BF 4 at room temperature
inferred← citeshttps://doi.org/10.1039/c4cs00253aopenalex-snapshot
Metal-mediated post-Ugi transformations for the construction of diverse heterocyclic scaffolds
inferred← citeshttps://doi.org/10.1039/c4ob00825aopenalex-snapshot
Triflic acid-promoted cycloisomerization of 2-alkynylphenyl isothiocyanates and isocyanates: a novel synthetic method for a variety of indole derivatives
inferred← citeshttps://doi.org/10.1039/c4ra02091jopenalex-snapshot
Three component synthesis of 2-oxindole via sequential Michael addition, intramolecular cyclization and aromatization
inferred← citeshttps://doi.org/10.1039/c5dt03794hopenalex-snapshot
1,1′-Bis(di-tert-butylphosphino)ferrocene copper( i ) complex catalyzed C–H activation and carboxylation of terminal alkynes
inferred← citeshttps://doi.org/10.1039/c5nj02630jopenalex-snapshot
Metal–organic framework MIL-101 supported bimetallic Pd–Cu nanocrystals as efficient catalysts for chromium reduction and conversion of carbon dioxide at room temperature
inferred← citeshttps://doi.org/10.1039/c7nj03038jopenalex-snapshot
cis -1,2-Bis(diphenylphosphino)ethylene copper( i ) catalyzed C–H activation and carboxylation of terminal alkynes
inferred← citeshttps://doi.org/10.1039/c7ob01142copenalex-snapshot
Direct access to isoxazolino and isoxazolo benzazepines from 2-((hydroxyimino)methyl)benzoic acid via a post-Ugi heteroannulation
inferred← citeshttps://doi.org/10.1039/c9ob02337bopenalex-snapshot
Facile synthesis of 2-alkynyl oxazoles via a Ce(OTf) 3 -catalyzed cascade reaction of alkynyl carboxylic acids with tert -butyl isocyanide
inferred← citeshttps://doi.org/10.1039/d3ra02065gopenalex-snapshot
Highly regioselective and diastereoselective synthesis of novel pyrazinoindolones via a base-mediated Ugi- N -alkylation sequence
inferred← citeshttps://doi.org/10.1039/d6nj01211fopenalex-snapshot
Transition metal complexes of trans -1,2-bis(diphenylphosphino)ethylene: structural insights and carboxylation of terminal alkynes with carbon dioxide
inferred← citeshttps://doi.org/10.1039/d6ra06856aopenalex-snapshot
Diastereoselective synthesis of tetrahydroisoquinolines through the Pd-catalyzed post-Ugi transformations
inferred← citeshttps://doi.org/10.1055/a-2837-6670openalex-snapshot
One-Pot Site-Selective Synthesis of 7-Arylidenefuro[3,4-b]pyridin-5(7H)-one Hybrids
inferred← citeshttps://doi.org/10.1070/rcr5010openalex-snapshot
Access to molecular complexity. Multicomponent reactions involving five or more components
inferred← citeshttps://doi.org/10.1080/17518253.2012.709280openalex-snapshot
Efficient synthesis of 2-amino-4-aryl-8-[(E)-arylmethylidene]-5, 6, 7, 8-4Hpyrano [3, 2-c]pyridine in green media
inferred← citeshttps://doi.org/10.1134/s1070428015120039openalex-snapshot
Nucleophilic addition of heterocyclic amines to conjugated enyne ketones
inferred← citeshttps://doi.org/10.1246/cl.2010.1132openalex-snapshot
Stereoselective Synthesis of 3-(1-Cyanoalkylidene)oxindoles by Palladium-catalyzed Cyclization Reaction of 2-(Alkynyl)aryl Isocyanates with Copper(I) Cyanide
inferred← citeshttps://doi.org/10.3390/app5041803openalex-snapshot
Sequentially Palladium-Catalyzed Processes in One-Pot Syntheses of Heterocycles
inferred← citeshttps://doi.org/10.3390/inorganics12110283openalex-snapshot
Catalytic Behavior of NHC–Silver Complexes in the Carboxylation of Terminal Alkynes with CO2
inferred← citeshttps://doi.org/10.3987/com-18-13975openalex-snapshot
Palladium-Catalyzed One-Pot Approach to 3-(1,3-Diarylprop-2-yn-1-ylidene)oxindoles
inferred← citeshttps://doi.org/10.4236/ijoc.2012.21006openalex-snapshot
A New and Efficient Method for the Synthesis of Pyrimido[2,1-b]Benzothiazole Derivatives
inferred← citeshttps://doi.org/10.4236/ijoc.2012.23037openalex-snapshot
Facile One-Pot Synthesis of Novel Hexahydro-2-quinolinecarboxylic Acids under Solvent-Free Reaction Conditions
inferred← citeshttps://doi.org/10.5012/jkcs.2014.58.2.186openalex-snapshot
Efficient Synthesis of Novel 3-Substituted Coumarin-3-carboxamide
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