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Novel One-Pot, Three-Component Synthesis of Spiro[Indoline-pyrazolo[4′,3′:5,6]pyrido[2,3-d]pyrimidine]trione Library
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Multicomponent Reactions with Isocyanides
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A facile three‐components, one‐pot synthesis of pyrimido[4,5‐d]pyrimidine‐2,5‐dione derivatives under microwave‐assisted conditions
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Selective catalytic synthesis of fine chemicals: opportunities and trends
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Synthesis and evaluation of some new spiro indoline-based heterocycles as potentially active antimicrobial agents
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Trifluoromethylpyrimidine-based inhibitors of proline-rich tyrosine kinase 2 (PYK2): Structure–activity relationships and strategies for the elimination of reactive metabolite formation
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A novel and efficient synthesis of pyrimido[4,5-d]pyrimidine-2,4,7-trione and pyrido[2,3-d:6,5-d] dipyrimidine-2,4,6,8-tetrone derivatives
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Specific phosphorylation of 5-ethyl-2′-deoxyuridine by herpes simplex virus-infected cells and incorporation into viral DNA.
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Silica Sulfuric Acid as an Efficient and Reusable Catalyst for the Pechmann Synthesis of Coumarins under Solvent-Free Conditions
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An Efficient Three-Component, One-Pot Synthesis of New Pyrimido[4,5-d]pyrimidine-2,4-diones
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Green Regioselective Synthesis of Novel Photo-And Thermochromic Spiro[Indoline-Pyrido-Pyrimidine] Derivatives and Computational Study of Their Structural Parameters
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Microwave-assisted multicomponent synthesis of spiro[indoline-3,4'-pyrazolo[3,4-b]quinoline]-2,5'(6'H)-diones catalyzed by Ionic liquid-coated magnetic carbon nanotubes
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Synthesis of Spirooxindoles by Multicomponent Reactions
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Recent Advances in Diversity Oriented Synthesis through Isatin‐based Multicomponent Reactions
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Nickel supported on magnetic biochar as a highly efficient and recyclable heterogeneous catalyst for the one‐pot synthesis of spirooxindole‐dihydropyridines
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Optimizing the Electrochemiluminescence of Readily Accessible Pyrido[1,2‐α]pyrimidines through “Green” Substituent Regulation
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Highly Efficient Construction of Bisspirooxindoles Containing Vicinal Spirocenters through an Organocatalytic Modified Feist–Bénary Reaction
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ChemInform Abstract: Novel One‐Pot, Three‐Component Synthesis of Spiro[indoline‐pyrazolo[4′,3′:5,6]pyrido[2,3‐d]pyrimidine]trione Library.
inferred← citeshttps://doi.org/10.1002/chin.201514294openalex-snapshot
ChemInform Abstract: Ultrasound‐Promoted Synthesis of Indole‐Appended Heterocycles
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Efficient Synthesis of the Functionalized Spiro[indoline‐3,4′‐pyridine] via Four‐component Reaction
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An Efficient Four‐component Synthesis of Spiro[indoline‐pyrazolo[4′,3′:5,6]pyrido[2,3‐d]pyrimidine]triones
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Synthesis of Spiro[indoline‐3,2′‐quinoline] Derivatives through a Four‐Component Reaction
inferred← citeshttps://doi.org/10.1002/ejoc.201200269openalex-snapshot
Molecular Diversity of Three‐Component Reactions of N‐Benzylbenzimidazolium Salts, Isatin, and Malononitrile or Ethyl Cyanoacetate
inferred← citeshttps://doi.org/10.1002/hlca.201000307openalex-snapshot
Organic Reaction in Water: A Highly Efficient and Environmentally Friendly Synthesis of Spiro Compounds Catalyzed by L ‐Proline
inferred← citeshttps://doi.org/10.1002/hlca.201100019openalex-snapshot
Isocyanide‐Based Three‐Component Synthesis of Pyrano‐pyrido‐quinoxalines
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One‐Pot Synthesis of 5,7,8,9,9a,10‐Hexahydro‐8‐thioxotetrahydropyrido[2,3‐d : 6,5‐d′]dipyrimidine‐2,4,6(1H,3H,5aH)‐triones via a Four‐Component Coupling Reaction of Aldehydes, Amines, Barbituric Acids, and Thiouracil
inferred← citeshttps://doi.org/10.1002/jhet.1010openalex-snapshot
A New Reaction of Isatin, Cyclic 1,3‐Diketone, and 2‐Cyanoacetamide: A Four‐Component Synthesis of Spirooxindoles
inferred← citeshttps://doi.org/10.1002/jhet.1041openalex-snapshot
Synthesis of New Tetrahydro‐1,5‐benzodiazepin‐3‐yl‐2‐phenylacetamides via Isocyanide‐Based Multicomponent Reactions
inferred← citeshttps://doi.org/10.1002/jhet.1537openalex-snapshot
Microwave-assisted Aqueous Multicomponent Reaction: Facile Synthesis of Polyfunctionalized Indoline-spiro Fused Pyran Derivatives
inferred← citeshttps://doi.org/10.1002/jhet.1681openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jhet.2138openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jhet.2596openalex-snapshot
Iodine/Water Mediated Parallel Synthesis of Bioactive Diversely Substituted Pyrazolo‐Pyrido‐Pyrimidines and Its Spiro Analogues: An Enviro‐Economic Approach
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Three‐Component Synthesis of Spiro[indoline‐3,4′‐pyrazolo[3,4‐b]pyridines] under Microwave Irradiation
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An Efficient Synthesis of 1′,7′,8′,9′‐Tetrahydrospiro[indoline‐3,4′‐pyrazolo[3,4‐b]quinoline]‐2,5′(6′H)‐dione Derivatives in Aqueous Medium
inferred← citeshttps://doi.org/10.1002/jhet.399openalex-snapshot
One‐pot and three‐component synthesis of spiro[chromeno[2,3‐d] pyrimidine‐5,3′‐indoline]‐diones and spiro[chromeno[2,3‐c] pyrazole‐4,3′‐indoline]‐diones
inferred← citeshttps://doi.org/10.1002/jhet.4702openalex-snapshot
An efficient one‐pot synthesis of Spiro[indoline‐3,11′‐pyrazolo[3,4‐f]pyrimido[4,5‐b]quinoline] derivatives
inferred← citeshttps://doi.org/10.1002/jhet.654openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jhet.655openalex-snapshot
Three‐component synthesis of spiro[indoline‐3,5′‐pyrimido[4,5‐b]quinoline]‐triones in water
inferred← citeshttps://doi.org/10.1002/jhet.833openalex-snapshot
Expeditious Synthesis and Single Crystal Structure of New Pyrazole‐Fused 1,4‐Oxazine
inferred← citeshttps://doi.org/10.1002/jhet.898openalex-snapshot
A Novel Method for the Synthesis of Spiro[indoline‐Pyrazolo[4′,3′:5,6]pyrido[2,3‐d]pyrimidine]triones by Alum as a Reusable Catalyst
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Recent Advances in Green Synthesis of 3,3′‐Spirooxindoles via Isatin–based One–pot Multicomponent Cascade Reactions in Aqueous Medium
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A Quick, Simple and Clean Synthesis of Spiro(indoline‐3,4′‐pyrazolo[4′, 3′:5,6]pyrido[2, 3‐d]pyrimidines) in Water through a Novel One‐Pot Multicomponent Reaction
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A Molecular Hybridization Approach for Simple and Expeditious Synthesis of Novel Spiro[oxindoline‐3, 4′‐isoxazolo[5, 4‐ b ]pyrazolo[4, 3‐ e ]pyridines] in Water
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Aminoazoles as Key Reagents in Multicomponent Heterocyclizations
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inferred← citeshttps://doi.org/10.1007/s11030-015-9629-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12039-013-0552-1openalex-snapshot
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Selective synthesis of novel pyridopyrimido annulated analogues of azepinones from Beckmann rearrangement of corresponding oximes by the 2,4,6-trichloro-1,3,5-triazine and dimethyl formamide reagent
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inferred← citeshttps://doi.org/10.1007/s13738-012-0187-zopenalex-snapshot
A mild and green chemistry approach for the synthesis of symmetrical spirooxindole derivatives
inferred← citeshttps://doi.org/10.1016/b978-0-08-096805-6.00013-9openalex-snapshot
Six-Membered Ring Systems
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Synthesis of novel spirooxindoles in water by using MnFe2O4 nanoparticles as an efficient magnetically recoverable and reusable catalyst
inferred← citeshttps://doi.org/10.1016/j.bmc.2016.02.019openalex-snapshot
Application of PEG-400 as a green biodegradable polymeric medium for the catalyst-free synthesis of spiro-dihydropyridines and their use as acetyl and butyrylcholinesterase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmcl.2013.04.068openalex-snapshot
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Combinatorial Chemistry Online
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A simple and catalyst-free three-component method for the synthesis of spiro[indenopyrazolopyridine indoline]diones and spiro[indenopyridopyrimidine indoline]triones
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Synthesis of fluorescent hydroxyl naphthalene-1,4-dione derivatives by a three-component reaction in water
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.04.040openalex-snapshot
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Choline chloride and lactic acid: A natural deep eutectic solvent for one-pot rapid construction of spiro[indoline-3,4′-pyrazolo[3,4-b]pyridines]
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inferred← citeshttps://doi.org/10.1016/j.tet.2011.03.020openalex-snapshot
New four-component reactions in water: a convergent approach to the metal-free synthesis of spiro[indoline/acenaphthylene-3,4′-pyrazolo[3,4-b]pyridine derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2012.07.073openalex-snapshot
A one-pot, three-component synthesis of spiro[indoline-isoxazolo[4′,3′:5,6]pyrido[2,3-d]pyrimidine]triones in water
inferred← citeshttps://doi.org/10.1016/j.tet.2012.08.030openalex-snapshot
Synthesis of the functionalized spiro[indoline-3,5′-pyrroline]-2,2′-diones via three-component reactions of arylamines, acetylenedicarboxylates, and isatins
inferred← citeshttps://doi.org/10.1016/j.tet.2014.09.048openalex-snapshot
Efficient synthesis of novel tricyclic fused pyranothiazolopyrimidine derivatives via isocyanide-based three-component reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2018.05.020openalex-snapshot
An expeditious access of 2,5′-dioxo-5′,6′,7′,8′-tetrahydro-1′H-spiro[indoline-3,4′-quinoline]-3′-carboxylate by reaction of isatin, ethyl cyanoacetate and enaminone in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.11.041openalex-snapshot
Grindstone chemistry: one-pot synthesis of spiro[diindenopyridine-indoline]triones and spiro[acenaphthylene-diindenopyridine]triones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.06.014openalex-snapshot
Pseudo four-component synthesis of benzopyranopyrimidines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.09.090openalex-snapshot
New HA 14-1 analogues: synthesis of 2-amino-4-cyano-4H-chromenes
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An efficient one-pot three-component synthesis of functionalized pyrimido[4,5-b]quinolines and indeno fused pyrido[2,3-d]pyrimidines in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.04.001openalex-snapshot
Aqua mediated indium(III) chloride catalyzed synthesis of fused pyrimidines and pyrazoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.05.019openalex-snapshot
A novel organocatalytic multi-component reaction: an efficient synthesis of polysubstituted pyrano-fused spirooxindoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.05.023openalex-snapshot
Synthesis of 1′-aryl-2′-(2-oxoindolin-3-yl)spiro[indoline-3,5′-pyrroline]-2,3′-dione via one-pot reaction of arylamines, acetone, and isatins
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.07.117openalex-snapshot
One pot four-component reaction for the efficient synthesis of spiro[indoline-3,4′-pyrano[2,3-c]pyrazole]-3′-carboxylate derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.01.028openalex-snapshot
One-pot three-component reaction for the synthesis of biologically important spiro[benzo[f]quinoline-3,3′-indoline] derivatives
inferred← citeshttps://doi.org/10.1016/j.ultsonch.2009.09.009openalex-snapshot
Ultrasound-assisted one-pot, three-component synthesis of spiro[indoline-3,4′-pyrazolo[3,4-b]pyridine]-2,6′(1′H)-diones in water
inferred← citeshttps://doi.org/10.1016/j.ultsonch.2009.11.017openalex-snapshot
Ultrasound-assisted three-component synthesis of 3-(5-amino-1H-pyrazol-4-yl)-3-(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-enyl)indolin-2-ones in water
inferred← citeshttps://doi.org/10.1016/j.ultsonch.2010.07.010openalex-snapshot
Ultrasound-assisted synthesis of 2,2′-(2-oxoindoline-3,3-diyl)bis(1H-indene-1,3(2H)-dione) derivatives
inferred← citeshttps://doi.org/10.1016/j.ultsonch.2014.05.013openalex-snapshot
Rapid and efficient one-pot synthesis of spiro[indoline-3,4′-pyrano[2, 3-c]pyrazole] derivatives catalyzed by l-proline under ultrasound irradiation
inferred← citeshttps://doi.org/10.1016/s0959-6380(11)22013-0openalex-snapshot
Six-Membered Ring Systems:
inferred← citeshttps://doi.org/10.1021/cc100017fopenalex-snapshot
One-Pot Combinatorial Synthesis of 4-Aryl-1H-thiopyrano[3,4-b]pyridine-5-one Derivatives
inferred← citeshttps://doi.org/10.1021/cc100056popenalex-snapshot
Efficient One-Pot Synthesis of Novel Spirooxindole Derivatives via Three-Component Reaction in Aqueous Medium
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Novel, One-Pot, Three-Component Route to Indol-3-yl Substituted Spirooxindole Derivatives
inferred← citeshttps://doi.org/10.1021/cc100128wopenalex-snapshot
Comprehensive Survey of Chemical Libraries for Drug Discovery and Chemical Biology: 2009
inferred← citeshttps://doi.org/10.1021/cc900130aopenalex-snapshot
One-Pot, Pseudo Four-Component Synthesis of a Spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-indoline]-trione Library
inferred← citeshttps://doi.org/10.1021/cc900169popenalex-snapshot
Simple and Catalyst-Free Synthesis of Oxoindolin-3-yl Phosphonates
inferred← citeshttps://doi.org/10.1021/co1000053openalex-snapshot
Simple Three-Component Method for the Synthesis of Spiroindeno[1,2-b]pyrido[2,3-d]pyrimidine-5,3′-indolines
inferred← citeshttps://doi.org/10.1021/co200128kopenalex-snapshot
Rapid and Efficient Ultrasound-Assisted Method for the Combinatorial Synthesis of Spiro[indoline-3,4′-pyrano[2,3-c]pyrazole] Derivatives
inferred← citeshttps://doi.org/10.1021/co300042vopenalex-snapshot
One-Pot, Three-Component Synthesis of 7-Azaindole Derivatives from N-Substituted 2-Amino-4-cyanopyrroles, Various Aldehydes, and Active Methylene Compounds
inferred← citeshttps://doi.org/10.1021/co300047jopenalex-snapshot
Synthesis of 2,6′-Dioxo-1′,5′,6′,7′-tetrahydrospiro[indoline-3,4′-pyrazolo[3,4- b ]pyridine]-5′-carbonitriles via a One-Pot, Three-Component Reaction in Water
inferred← citeshttps://doi.org/10.1021/co3001204openalex-snapshot
One-Pot Three-Component Synthesis of Pyrano [3,2-b]pyrazolo[4,3-e]pyridin-8(1H)-ones
inferred← citeshttps://doi.org/10.1021/co400057hopenalex-snapshot
Copper Ferrite Nanoparticles: An Efficient and Reusable Nanocatalyst for a Green One-Pot, Three-component Synthesis of Spirooxindoles in Water
inferred← citeshttps://doi.org/10.1021/co400096copenalex-snapshot
Efficient and Regioselective Synthesis of Novel Functionalized Dispiropyrrolidines and Their Cytotoxic Activities
inferred← citeshttps://doi.org/10.1039/c2gc35635jopenalex-snapshot
Multicomponent reactions in unconventional solvents: state of the art
inferred← citeshttps://doi.org/10.1039/c2ob26849copenalex-snapshot
Facile synthesis of spiro[indoline-3,3′-pyrrolo[1,2-a]quinolines] and spiro[indoline-3,1′-pyrrolo[2,1-a]isoquinolines] via 1,3-dipolar cycloaddition reactions of heteroaromatic ammonium salts with 3-phenacylideneoxindoles
inferred← citeshttps://doi.org/10.1039/c4dt02038copenalex-snapshot
Inorganic–organic hybrid silica based tin complex as a novel, highly efficient and recyclable heterogeneous catalyst for the one-pot preparation of spirooxindoles in water
inferred← citeshttps://doi.org/10.1039/c4ra07860hopenalex-snapshot
Organocatalytic domino Michael/cyclization reaction: efficient synthesis of multi-functionalized tetracyclic spirooxindoles with multiple stereocenters
inferred← citeshttps://doi.org/10.1039/c5ob01484kopenalex-snapshot
A facile approach to the synthesis of structurally diverse 6,8a-dihydropyrido[2,3-d]pyrimidine derivatives via a three-component domino reaction
inferred← citeshttps://doi.org/10.1039/c5ra16769hopenalex-snapshot
Facile, novel and efficient synthesis of new pyrazolo[3,4-b]pyridine products from condensation of pyrazole-5-amine derivatives and activated carbonyl groups
inferred← citeshttps://doi.org/10.1039/c6ra05322jopenalex-snapshot
A catalyst-free, one-pot multicomponent synthesis of spiro-benzimidazoquinazolinones via a Knoevenagel–Michael-imine pathway: a microwave assisted approach
inferred← citeshttps://doi.org/10.1039/c8nj04921aopenalex-snapshot
Nano-2-(dimethylamino)- N -(silica- n -propyl)- N , N -dimethylethanaminium chloride as a novel basic catalyst for the efficient synthesis of pyrido[2,3- d :6,5- d ′]dipyrimidines
inferred← citeshttps://doi.org/10.1039/d2ra07521kopenalex-snapshot
A new and straightforward route to synthesize novel pyrazolo[3,4- b ]pyridine-5-carboxylate scaffolds from 1,4-dihydropyrano[2,3- c ]pyrazole-5-carbonitriles
inferred← citeshttps://doi.org/10.1039/d5ob01786fopenalex-snapshot
Green and sustainable nanocatalyzed syntheses of hybrid heterocyclic scaffolds with privileged substructures
inferred← citeshttps://doi.org/10.1080/00397911.2018.1447672openalex-snapshot
Diversity-oriented regioselective domino Michael/Aldol reaction of 3-ylideneoxindoles: A direct access to indanol-fused 3-oxindoles
inferred← citeshttps://doi.org/10.1080/10406638.2019.1705360openalex-snapshot
Synthesis and Application of Imidazolium-Based Ionic Liquid Supported on Hydroxyapatite Encapsulated γ-Fe 2 O 3 Nanocatalyst in Preparation of Pyrido[2,3- d ]Pyrimidines
inferred← citeshttps://doi.org/10.1080/10426507.2013.788004openalex-snapshot
Cufe2O4Nanoparticles: A Magnetically Retrievable Catalyst for Green Synthesis of Novel 2-(3-(Dicyanomethyl)-2-Oxoindolin-3-Ylthio)Acetic Acids
inferred← citeshttps://doi.org/10.1155/2020/8021920openalex-snapshot
Synthesis of New Oxindoles and Determination of Their Antibacterial Properties
inferred← citeshttps://doi.org/10.1248/cpb.58.516openalex-snapshot
Chromeno[2,3-d]pyrimidine-triones Synthesis by a Three-Component Coupling Reaction
inferred← citeshttps://doi.org/10.1248/cpb.58.896openalex-snapshot
Three-Component Synthesis of 2-Oxoindolin-3-ylphosphonates
inferred← citeshttps://doi.org/10.1371/journal.pone.0181241openalex-snapshot
New hydrazonoindolin-2-ones: Synthesis, exploration of the possible anti-proliferative mechanism of action and encapsulation into PLGA microspheres
inferred← citeshttps://doi.org/10.21203/rs.3.rs-5190730/v1openalex-snapshot
Microwave-assisted multicomponent synthesis of spiro[indoline-3,4'-pyrazolo[3,4-b]quinoline]-2,5'(6'H)-diones catalyzed by Ionic liquid-coated magnetic carbon nanotubes
inferred← citeshttps://doi.org/10.2174/1385272823666190717101741openalex-snapshot
Ionic Liquids for the Synthesis of Five-Membered N,N-, N,N,N- and N,N,N,NHeterocycles
inferred← citeshttps://doi.org/10.2174/2213337210666230224114001openalex-snapshot
Review on the Synthesis of Bio-Active Spiro-Fused Heterocyclic Molecules
inferred← citeshttps://doi.org/10.24959/ophcj.18.950openalex-snapshot
Domino-reactions of isatins with 5-aminopyrazoles and 2,2-dimethyl-1,3-dioxane-4,6-dione
inferred← citeshttps://doi.org/10.3184/174751911x13157531279974openalex-snapshot
An Efficient, One-Pot Synthesis of Spiro[Dihydropyridine-Oxindole] Compounds under Catalyst-Free Conditions
inferred← citeshttps://doi.org/10.3184/174751915x14316237301775openalex-snapshot
Synthesis of Polysubstituted Pyrroles Derivatives by PPh 3 -Promoted Condensation Reaction between Ninhydrin, 2-Amino Pyridine Derivatives and Acetylenes
inferred← citeshttps://doi.org/10.3390/chemistry7010018openalex-snapshot
Pyrrolizine- and Indolizine-Derived Spirooxindoles: Synthesis, Antibacterial Activity and Inverse Docking Analysis
inferred← citeshttps://doi.org/10.3390/molecules25245862openalex-snapshot
Grindstone Chemistry: Design, One-Pot Synthesis, and Promising Anticancer Activity of Spiro[acridine-9,2′-indoline]-1,3,8-trione Derivatives against the MCF-7 Cancer Cell Line
inferred← citeshttps://doi.org/10.3390/org5030017openalex-snapshot
A Review on Barbituric Acid and Its Derivatives: Synthesis, Reactions, and Bio-Applications
inferred← citeshttps://doi.org/10.3762/bjoc.9.2openalex-snapshot
Synthesis of spiro[dihydropyridine-oxindoles] via three-component reaction of arylamine, isatin and cyclopentane-1,3-dione
inferred← citeshttps://doi.org/10.5772/51937openalex-snapshot
Multicomponent Reactions in Ionic Liquids
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