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Highly Selective Domino Multicyclizations for Forming Polycyclic Fused Acridines and Azaheterocyclic Skeletons

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/9783527609925openalex-snapshot
Domino Reactions in Organic Synthesis
inferredcites →https://doi.org/10.1002/jlac.198919890225openalex-snapshot
Photoaddition of 2‐Pyridones and 2‐Quinolones to Conjugated Dienes
inferredcites →https://doi.org/10.1016/j.tetlet.2012.06.070openalex-snapshot
An unexpected multicomponent reaction leading to 2-arylpyrrolo[2,3,4-kl]acridin-1(2H)-ones
inferredcites →https://doi.org/10.1016/s0026-895x(24)12507-2openalex-snapshot
Potent Inhibition of Telomerase by Small-Molecule Pentacyclic Acridines Capable of Interacting with G-Quadruplexes
inferredcites →https://doi.org/10.1016/s0040-4020(01)81215-1openalex-snapshot
The biomimetic synthesis of marine alkaloid related pyrido- and pyrrolo[2,3,4-kl]acridines
inferredcites →https://doi.org/10.1016/s0040-4039(00)79220-3openalex-snapshot
Scandium trifluoromethanesulfonate (Sc(OTf)3). A novel reusable catalyst in the Diels-Alder reaction
inferredcites →https://doi.org/10.1016/s0040-4039(00)89041-3openalex-snapshot
Plakinidines: Cytotoxic alkaloid pigments from the fijian sponge plakortis sp.
inferredcites →https://doi.org/10.1016/s0065-2725(08)60930-7openalex-snapshot
Heterocycle-Fused Acridines
inferredcites →https://doi.org/10.1021/ar0402356openalex-snapshot
Arylation Reactions: The Photo-SN1 Path via Phenyl Cation as an Alternative to Metal Catalysis
inferredcites →https://doi.org/10.1021/ar8000298openalex-snapshot
Copper/Amino Acid Catalyzed Cross-Couplings of Aryl and Vinyl Halides with Nucleophiles
inferredcites →https://doi.org/10.1021/ar800170yopenalex-snapshot
The Domino Multicomponent Allylation Reaction for the Stereoselective Synthesis of Homoallylic Alcohols
inferredcites →https://doi.org/10.1021/ar800214sopenalex-snapshot
Strategies for Innovation in Multicomponent Reaction Design
inferredcites →https://doi.org/10.1021/cr040623lopenalex-snapshot
A Case Study in Biomimetic Total Synthesis: Polyolefin Carbocyclizations to Terpenes and Steroids
inferredcites →https://doi.org/10.1021/cr950027eopenalex-snapshot
Domino Reactions in Organic Synthesis
inferredcites →https://doi.org/10.1021/ja00079a033openalex-snapshot
Diastereoselective cycloisomerizations of enediynes via palladium catalysis
inferredcites →https://doi.org/10.1021/ja00157a001openalex-snapshot
Novel marine sponge alkaloids. 1. Plakinidine A and B, anthelmintic active alkaloids from a Plakortis sponge
inferredcites →https://doi.org/10.1021/ja055735oopenalex-snapshot
Catalytic Asymmetric Reductive Michael Cyclization
inferredcites →https://doi.org/10.1021/ja1034123openalex-snapshot
Gold-Catalyzed Three-Component Coupling: Oxidative Oxyarylation of Alkenes
inferredcites →https://doi.org/10.1021/ja3111626openalex-snapshot
Access to the Akuammiline Family of Alkaloids: Total Synthesis of (+)-Scholarisine A
inferredcites →https://doi.org/10.1021/ja806183ropenalex-snapshot
Total Synthesis of Diverse Carbogenic Complexity within the Resveratrol Class from a Common Building Block
inferredcites →https://doi.org/10.1021/ja904011sopenalex-snapshot
Four-Component Domino Reaction Leading to Multifunctionalized Quinazolines
inferredcites →https://doi.org/10.1021/ja906468vopenalex-snapshot
A Tandem Cascade Cyclization−Electrophilic Aromatic Substitution: Application in the Total Synthesis of (+)-Angelichalcone
inferredcites →https://doi.org/10.1021/ja980715qopenalex-snapshot
Lewis Acid Catalysts Stable in Water. Correlation between Catalytic Activity in Water and Hydrolysis Constants and Exchange Rate Constants for Substitution of Inner-Sphere Water Ligands
inferredcites →https://doi.org/10.1021/ja992411popenalex-snapshot
An Exceptionally Short and Simple Enantioselective Total Synthesis of Pentacyclic Triterpenes of the β-Amyrin Family
inferredcites →https://doi.org/10.1021/jm049706kopenalex-snapshot
Rational Design, Synthesis, and Biological Evaluation of Bis(pyrimido[5,6,1-de]acridines) and Bis(pyrazolo[3,4,5-kl]acridine-5-carboxamides) as New Anticancer Agents
inferredcites →https://doi.org/10.1021/jm058031yopenalex-snapshot
Antitumor Polycyclic Acridines. 17. Synthesis and Pharmaceutical Profiles of Pentacyclic Acridinium Salts Designed To Destabilize Telomeric Integrity
inferredcites →https://doi.org/10.1021/jm9909490openalex-snapshot
Antitumor Polycyclic Acridines. 7. Synthesis and Biological Properties of DNA Affinic Tetra- and Pentacyclic Acridines
inferredcites →https://doi.org/10.1021/jo00031a035openalex-snapshot
Pyridoacridine alkaloids from deep-water marine sponges of the family Pachastrellidae: structure revision of dercitin and related compounds and correlation with the kuanoniamines
inferredcites →https://doi.org/10.1021/jo00950a023openalex-snapshot
Unsaturated heterocyclic systems. LXXXIX. Reactivity of bicyclo [4.2.2] deca-2,4,7,9-tetraene derivatives under conditions of uniparticulate electrophilic addition. Intramolecular capture of zwitterionic bridged 1,4-bishomotropylium (bicyclo [4.3.1] deca-2,4,7-trienyl) intermediates
inferredcites →https://doi.org/10.1021/jo01034a531openalex-snapshot
Some Diels—Alder Studies of the 1,3-Dihydro-2H-azepin-2-ones1
inferredcites →https://doi.org/10.1021/jo049808iopenalex-snapshot
A New Strategy toward Indole Alkaloids Involving an Intramolecular Cycloaddition/Rearrangement Cascade
inferredcites →https://doi.org/10.1021/jo1002278openalex-snapshot
Four-Component Domino Reaction Providing an Easy Access to Multifunctionalized Tricyclo[6.2.2.01,6]dodecane Derivatives
inferredcites →https://doi.org/10.1021/jo8016956openalex-snapshot
Cycloaddition Across the Benzofuran Ring as an Approach to the Morphine Alkaloids
inferredcites →https://doi.org/10.1021/jo9003579openalex-snapshot
Conjugate Addition−Dipolar Cycloaddition Cascade for the Synthesis of Benzo[a]quinolizine and Indolo[a]quinolizine Scaffolds: Application to the Total Synthesis of (±)-Yohimbenone
inferredcites →https://doi.org/10.1021/jo902204sopenalex-snapshot
Microwave Enabled Umpulong Mechanism Based Rapid and Efficient Four- and Six-Component Domino Formations of 2-(2′-Azaaryl)imidazoles and anti-1,2-Diarylethylbenzamides
inferredcites →https://doi.org/10.1021/ol201479popenalex-snapshot
Facile Sc(OTf)3-Catalyzed Generation and Successive Aromatization of Isobenzofuran from o-Dicarbonylbenzenes
inferredcites →https://doi.org/10.1021/ol203166copenalex-snapshot
Efficient Domino Approaches to Multifunctionalized Fused Pyrroles and Dibenzo[b,e][1,4]diazepin-1-ones
inferredcites →https://doi.org/10.1021/ol300582yopenalex-snapshot
Synthesis of Water-Soluble Phosphine Oxides by Pd/C-Catalyzed P–C Coupling in Water
inferredcites →https://doi.org/10.1021/ol302058gopenalex-snapshot
An Efficient Synthesis of Pyrrolo[2,3,4-kl]acridin-1-one Derivatives Catalyzed by l -Proline
inferredcites →https://doi.org/10.1021/ol702453qopenalex-snapshot
C−C Bond Formation Catalyzed Heterogeneously by Nickel-on-Graphite (Ni/Cg)
inferredcites →https://doi.org/10.1039/b303362gopenalex-snapshot
The domino intramolecular Diels–Alder approach to 16-oxasteroids
inferredcites →https://doi.org/10.1039/b816701jopenalex-snapshot
Domino reactions of rhodium(ii) carbenoids for alkaloid synthesis
inferredcites →https://doi.org/10.1039/c2ob26315gopenalex-snapshot
A domino synthetic strategy leading to two-carbon-tethered fused acridine/indole pairs and fused acridine derivatives
inferredcites →https://doi.org/10.1071/ch09126openalex-snapshot
Naturally Occurring Nitrogen–Sulfur Compounds. The Benzothiazole Alkaloids
inferredcites →https://doi.org/10.1080/14786410601132212openalex-snapshot
Nordehydrocyclodercitin, a hexacyclic pyridoacridine alkaloid from the marine ascidian,Aplidiumsp.
inferredcites →https://doi.org/10.1126/science.1067074openalex-snapshot
Remarkably Selective Iridium Catalysts for the Elaboration of Aromatic C-H Bonds

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4761082openalex-extracted
I2-Catalyzed Cascade Annulation of 2-(Pyridin-2-Yl)Acetate Derivatives with N,N-Dimethylenamine Ketones: Site-Selective Synthesis of Functionalized Indolizines
inferred← citeshttps://doi.org/10.2139/ssrn.4798967openalex-extracted
Radical Cascade Reaction of Heterocyclic Ketene Aminals with Thiocyanates Promoted by Visible Light: Environmentally Fridendly Synthesis of Functionalized Fused 2-Iminothiazolines
inferred← citeshttps://doi.org/10.1002/9783527809080.cataz11194openalex-snapshot
multicyclization
inferred← citeshttps://doi.org/10.1002/adsc.201701610openalex-snapshot
I2‐Triggered Reductive Generation of N‐Centered Iminyl Radicals: An Isatin‐to‐Quinoline Strategy for the Introduction of Primary Amides
inferred← citeshttps://doi.org/10.1002/adsc.202100633openalex-snapshot
Copper(II)‐Mediated Intermolecular Radical [3+2]‐Annulation of N,N‐Dimethyl Enaminones: Direct Access to 5‐Acyl‐3‐Furancarboxaldehydes
inferred← citeshttps://doi.org/10.1002/ajoc.201500159openalex-snapshot
Selective Synthesis of Acenaphtho[1,2‐b]indole Derivatives via Tandem Regioselective Aza‐Ene Addition/N‐Cyclization/SN1 Type Reaction
inferred← citeshttps://doi.org/10.1002/ajoc.201600148openalex-snapshot
Site‐Selective Convergent Synthesis of Spiroacridines through a Cascade Reaction of Enaminones with Acenaphthoquinone: An Efficient Construction of Multiple C−C and C–Heteroatom Bonds
inferred← citeshttps://doi.org/10.1002/chin.201334159openalex-snapshot
ChemInform Abstract: Highly Selective Domino Multicyclizations for Forming Polycyclic Fused Acridines and Azaheterocyclic Skeletons.
inferred← citeshttps://doi.org/10.1002/ejoc.201402164openalex-snapshot
Efficient Domino Synthesis of Pyrrole‐Fused Isocoumarins with Microwave Heating
inferred← citeshttps://doi.org/10.1002/ejoc.201600163openalex-snapshot
Three‐Component Bicyclization Leading to Densely Functionalized Pyrazolo[3,4‐d]thiazolo[3,2‐a]pyrimidines
inferred← citeshttps://doi.org/10.1002/ejoc.201800734openalex-snapshot
Convenient Synthesis of Quinoline‐4‐carboxylate Derivatives through the Bi(OTf)3‐Catalyzed Domino Cyclization/Esterification Reaction of Isatins with Enaminones in Alcohols
inferred← citeshttps://doi.org/10.1002/ejoc.201901413openalex-snapshot
Coupling‐Isomerization‐Cycloisomerization Reaction (CICIR) – An Unexpected and Efficient Domino Approach to Luminescent 2‐(Hydroxymethylene)indenones
inferred← citeshttps://doi.org/10.1002/ejoc.202300183openalex-snapshot
β‐N‐Heterocyclic Cyclobutane Carboximides: Synthesis through a Tandem Base‐Catalyzed Amidation/aza‐Michael Addition Protocol and Facile Transformations
inferred← citeshttps://doi.org/10.1002/ejoc.202301000openalex-snapshot
Single Step Upgradation of Isatin to Bioactive Fused Heterocycles via Ring Expansion Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.70699openalex-snapshot
Synthetic Strategies for the Construction of Cyclobutane‐Fused Heterocycles
inferred← citeshttps://doi.org/10.1002/jhet.2345openalex-snapshot
Convenient Synthesis of Functionalized 3,4,10,11‐tetrahydroindolo[1,2‐a]Quinoxalines Via Three‐component Reaction of Dimedone, 3‐nitrochromenes and Ammonium Acetate
inferred← citeshttps://doi.org/10.1002/jhet.2437openalex-snapshot
Regioselectively Synthesis of Thiazolo[4,5‐a]acridines and Oxazolo[5,4‐a]thiazolo[5,4‐j]acridines via Multicomponent Domino Reactions
inferred← citeshttps://doi.org/10.1002/jhet.3592openalex-snapshot
An Efficient Five‐Component Reaction for the Synthesis of 4,4′‐((2‐Oxoindoline‐3,3‐diyl)bis(methylene))bis(2‐aryl‐1H‐pyrrolo[3,4‐c]quinoline‐1,3(2H)‐dione) Derivatives
inferred← citeshttps://doi.org/10.1002/slct.201702810openalex-snapshot
A Facile and Green Approach for One‐Pot Synthesis of Functionalized Chromeno[3, 4‐b]quinolines and Spiro Chromeno[3, 4‐b]quinolines by Using Molecular Iodine as a Catalyst
inferred← citeshttps://doi.org/10.1002/slct.201801176openalex-snapshot
Unactivated sp3 C‐H Functionalization by I2/DMSO: An Efficient Method to Synthesize Isatins†
inferred← citeshttps://doi.org/10.1002/slct.202304938openalex-snapshot
Synthesis of Polycyclic Pyrrolopyridine Derivatives via Multicomponent Synthesis of 1,5‐Diketones
inferred← citeshttps://doi.org/10.1002/tcr.201600018openalex-snapshot
Access to Spiro and Fused Indole Derivatives from α,β-Unsaturated Aldehydes Enabled by N-Heterocyclic Carbene Catalysis
inferred← citeshttps://doi.org/10.1002/tcr.70239openalex-snapshot
Serendipitous Emergence of Pyrrolo[2,3,4‐ kl ]acridin‐1(2 H )‐one Derivatives: From Unexpected Discovery to Synthetic Development
inferred← citeshttps://doi.org/10.1007/s11164-013-1396-5openalex-snapshot
Three-component domino [3+2] heterocyclization leading to pyran-3-yl-substituted fused pyrroles
inferred← citeshttps://doi.org/10.1016/b978-0-08-100017-5.00006-6openalex-snapshot
Five-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14899-1openalex-snapshot
Three Heterocyclic Rings Fused (5-6-5)
inferred← citeshttps://doi.org/10.1016/b978-0-443-18939-5.00006-8openalex-snapshot
Five-membered ring systems: pyrroles and benzo analogs
inferred← citeshttps://doi.org/10.1016/j.cclet.2014.03.022openalex-snapshot
Synthesis of hexacyclic fused isocoumarin framework through selective domino multicyclizations under catalyst and solvent free conditions
inferred← citeshttps://doi.org/10.1016/j.gresc.2021.10.008openalex-snapshot
An environmentally benign multi-component reaction: Highly regioselective synthesis of functionalized 2-(diarylphosphoryl)-1,2-dihydro-pyridine derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2014.11.005openalex-snapshot
Domino bicyclization of 2,2-dihydroxyindene-1,3-dione with cyclic enaminones leading to isochromeno[4,3-b]indoles
inferred← citeshttps://doi.org/10.1016/j.tet.2014.12.100openalex-snapshot
Three-component synthesis of functionalized pyrrolo[3,4-c]quinolin-1-ones by an unusual reductive cascade reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2016.03.026openalex-snapshot
Base-controlled 1,6-enyne-bicyclization: divergent synthesis of benzo[b]fluorenones and benzo[b]fluorenols
inferred← citeshttps://doi.org/10.1016/j.tet.2017.12.003openalex-snapshot
Catalyst-free concise synthesis of multi-functional 3-cyano-4-quinolinone derivatives from cyanoacetylenaminones and DMF-DMA
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.tet.2024.134015openalex-snapshot
I2−catalyzed cascade annulation of 2-(pyridin−2−yl)acetate derivatives with ,−dimethylenamine ketones: Site-selective synthesis of functionalized indolizines
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134289openalex-snapshot
Regioselective synthesis of functionalized cyclopent-2-enone-derived carbonylureas and enaminohydroxybarbiturates from alloxans in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.09.046openalex-snapshot
Efficient [4+1]/[3+2+1] bis-cyclizations stereoselectively yielding unprecedented polyacyclic indeno-fused xanthenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.10.151openalex-snapshot
Efficient three-component reactions of α-thiocyanato ketones stereoselectively forming E-3-aroylidene-2-oxindole derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.01.154openalex-snapshot
(±)-CSA catalyzed one-pot synthesis of 6,7-dihydrospiro[indole-3,1′-isoindoline]-2,3′,4(1H,5H)-trione derivatives: easy access of spirooxindoles and ibophyllidine-like alkaloids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.06.062openalex-snapshot
I2–DMSO promoted intramolecular oxidative cyclization of 2-(aryl or alkyl amino)-acetophenones for the synthesis of isatins
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.09.076openalex-snapshot
Direct copper(II)-mediated regioselective α-halogenation of N-aryl enaminones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.12.090openalex-snapshot
Cascade synthesis of selective dihydro pyridazino fused acridinone derivatives via MCM-41 catalyzed ring-opening/ring-closure reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.03.009openalex-snapshot
Regiospecific synthesis of 1,5,6,7-tetrahydro-4H-indol-4-ones via dehydroxylated [3+2] cyclization of β-hydroxy ketones with cyclic enaminones
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02645openalex-snapshot
Construction of Polyfunctionalized 2,4-Dioxa-8-azaspiro[5.5]undec-9-enes and 2,4,8-Triazaspiro[5.5]undec-9-enes via a Domino [2+2+2] Cycloaddition Reaction
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01899openalex-snapshot
Radical Cascade Reaction of Heterocyclic Ketene Aminals with Thiocyanates Promoted by Visible Light: Synthesis of Functionalized Fused 2-Iminothiazolines
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00581openalex-snapshot
Iodine-Mediated C–H Functionalization of sp, sp2, and sp3 Carbon: A Unified Multisubstrate Domino Approach for Isatin Synthesis
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00727openalex-snapshot
Synthesis of 3-Iminoindol-2-amines and Cyclic Enaminones via Palladium-Catalyzed Isocyanide Insertion-Cyclization
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00397openalex-snapshot
Fe(III)-Mediated Oxidative [5 + 1] Cyclization for the Highly Site-Selective Synthesis of Functionalized Quinoline Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02457openalex-snapshot
Construction of Unique Eight- or Nine-Membered Polyheterocyclic Systems via Multicomponent Reaction of l -Proline, Alkyl Propiolate, and Isatin
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02689openalex-snapshot
Cu(II)/Iodine(III) Oxide Dimerization of Heterocyclic Ketene Aminals: Tandem TEMPO Oxidation for the Highly Selective Synthesis of Functionalized 2 H -Pyrrolo[1,2- a ]imidazol-7(3 H )-ones
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00710openalex-snapshot
Highly Regioselective and Chemoselective [3 + 3] Annulation of Enaminones with ortho-Fluoronitrobenzenenes: Divergent Synthesis of Aposafranones and Their N-Oxides
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00751openalex-snapshot
Preparation of Thiazole-2-thiones through TBPB-Promoted Oxidative Cascade Cyclization of Enaminones with Elemental Sulfur
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c02431openalex-snapshot
Multicomponent Cascade Reaction of 3-Formylchromones: Highly Selective Synthesis of Functionalized 9-Azabicyclo[3.3.1]nonane Derivatives
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00095openalex-snapshot
Hydroxyl-Directed Rh(III)-Catalyzed C–H Functionalization: Access to Benzo[ de ]chromenes
inferred← citeshttps://doi.org/10.1021/acsomega.9b01002openalex-snapshot
Synthesis of Substituted Isatins from the MBH Adduct of 1,5,6-Trisubstituted Isatins Using (2,4-Dinitrophenyl)hydrazine and K-10 Clay Explored as Protection–Deprotection Chemistry
inferred← citeshttps://doi.org/10.1021/acsomega.9b01159openalex-snapshot
Three-Component One-Pot Synthesis of Highly Functionalized Bis-Indole Derivatives
inferred← citeshttps://doi.org/10.1021/co5000097openalex-snapshot
Efficient Domino Strategy for the Synthesis of Polyfunctionalized Benzofuran-4(5H)-ones and Cinnoline-4-carboxamides
inferred← citeshttps://doi.org/10.1021/jo500550dopenalex-snapshot
Direct Amidation of 2′-Aminoacetophenones Using I2-TBHP: A Unimolecular Domino Approach toward Isatin and Iodoisatin
inferred← citeshttps://doi.org/10.1021/jo501292qopenalex-snapshot
Diastereoselective Construction of Tetrahydropyridine Fused Bicyclic Structures via Three-Component Domino Reaction
inferred← citeshttps://doi.org/10.1021/jo502096topenalex-snapshot
Four-Component Bicyclization Approaches to Skeletally Diverse Pyrazolo[3,4- b ]pyridine Derivatives
inferred← citeshttps://doi.org/10.1021/ol402750ropenalex-snapshot
Copper-Mediated Selective C–H Activation and Cross-Dehydrogenative C–N Coupling of 2′-Aminoacetophenones
inferred← citeshttps://doi.org/10.1039/c3cc49191aopenalex-snapshot
ZnCl 2 -catalyzed chemoselective cascade reactions of enaminones with 2-furylcarbinols: a versatile process for the synthesis of cyclopenta[b]pyrrole derivatives
inferred← citeshttps://doi.org/10.1039/c3ob40791hopenalex-snapshot
Efficient one-step synthesis of pyrrolo[3,4-c]quinoline-1,3-dione derivatives by organocatalytic cascade reactions of isatins and β-ketoamides
inferred← citeshttps://doi.org/10.1039/c4cc00740aopenalex-snapshot
Four-component strategy for selective synthesis of azepino[5,4,3-cd]indoles and pyrazolo[3,4-b]pyridines
inferred← citeshttps://doi.org/10.1039/c4cc08257eopenalex-snapshot
Synthesis of enaminones and their difluoroboron complexes through domino aryl migration
inferred← citeshttps://doi.org/10.1039/c4cc08900fopenalex-snapshot
Highly selective synthesis of functionalized polyhydroisoquinoline derivatives via a three-component domino reaction
inferred← citeshttps://doi.org/10.1039/c4gc01832jopenalex-snapshot
Highly efficient construction of a bridged pentacyclic skeleton via a six-component domino reaction under microwave irradiation
inferred← citeshttps://doi.org/10.1039/c4ra06239fopenalex-snapshot
“On-water” synthesis of novel trisubstituted 1,3-thiazoles via microwave-assisted catalyst-free domino reactions
inferred← citeshttps://doi.org/10.1039/c4ra10096dopenalex-snapshot
Highly diastereoselective synthesis of quinoline-2,5-diones and pyrazolo[3,4-b]pyridin-6(7H)-ones under microwave irradiation
inferred← citeshttps://doi.org/10.1039/c4ra12560fopenalex-snapshot
Selective synthesis of polyfunctionalized hydroisoquinoline derivatives via a three-component domino reaction
inferred← citeshttps://doi.org/10.1039/c4ra16298fopenalex-snapshot
Microwave-assisted synthesis of novel 2,3-disubstituted imidazo[1,2-a]pyridines via one-pot three component reactions
inferred← citeshttps://doi.org/10.1039/c5cc04306aopenalex-snapshot
Cascade bicyclizations of o-alkynyl aldehydes with thiazolium salts: a new access toward poly-functionalized indeno[2,1-b]pyrroles
inferred← citeshttps://doi.org/10.1039/c5gc00156kopenalex-snapshot
Single step incorporation of carboxylic acid groups in the lower rim of calix[4]arenes: a recyclable catalyst towards assembly of diverse five ring fused acridines
inferred← citeshttps://doi.org/10.1039/c6cc02659aopenalex-snapshot
Insights into the unexpected chemoselectivity in Brønsted acid catalyzed cyclization of isatins with enaminones: convenient synthesis of pyrrolo[3,4-c]quinolin-1-ones and spirooxindoles
inferred← citeshttps://doi.org/10.1039/c6ra00476hopenalex-snapshot
Molecular diversity of the cyclization reaction of 3-methyleneoxindoles with 2-(3,4-dihydronaphthalen-1(2H)-ylidene)malononitriles
inferred← citeshttps://doi.org/10.1039/c6ra15492aopenalex-snapshot
Convenient one-step synthesis of pyrrolo[3,4-c]quinolin-1-ones via TMSCl-catalyzed cascade reactions of isatins and β-enamino ketones
inferred← citeshttps://doi.org/10.1039/c6ra18048eopenalex-snapshot
Single step incorporation of isatin to enaminone: a recyclable catalyst towards assembly of diverse four ring fused pyrrolo[2,3,4-kl]acridin-1-ones
inferred← citeshttps://doi.org/10.1039/c7nj02441jopenalex-snapshot
Copper-catalyzed aerobic oxidative intramolecular amidation of 2-aminophenylacetylenes: a domino process for the synthesis of isatin
inferred← citeshttps://doi.org/10.1039/c7ob00306dopenalex-snapshot
Efficient construction of C–N and C–S bonds in 2-iminothiazoles via cascade reaction of enaminones with potassium thiocyanate
inferred← citeshttps://doi.org/10.1039/c8cc04471fopenalex-snapshot
NaI-mediated divergent synthesis of isatins and isoindigoes: a new protocol enabled by an oxidation relay strategy
inferred← citeshttps://doi.org/10.1039/c8ra01236aopenalex-snapshot
Divergent synthesis of dual 1,4-dihydropyridines with different substituted patterns from enaminones and aldehydes through domino reactions
inferred← citeshttps://doi.org/10.1039/c9gc01120jopenalex-snapshot
A multicomponent two-step strategy for the synthesis of polysubstituted pyrrolo[3,2- c ]pyridin-4-ones using a solid acid as a recyclable catalyst
inferred← citeshttps://doi.org/10.1039/d0cc00923gopenalex-snapshot
Cascade reaction of isatins with nitro-substituted enamines: highly selective synthesis of functionalized ( Z )-3-(1-(arylamino)-2-oxoarylidene)indolin-2-ones
inferred← citeshttps://doi.org/10.1039/d2qo00473aopenalex-snapshot
Facile approach to multifunctionalized 5-alkylidene-3-pyrrolin-2-ones via regioselective oxidative cyclization of 2,4-pentanediones with primary amines and sodium sulfinates
inferred← citeshttps://doi.org/10.1039/d3ob00014aopenalex-snapshot
Access to thiionized-, selenolized-, and alkylated 5-alkylidene 3-pyrrolin-2-one derivatives via a regioselective oxidative annulation reaction
inferred← citeshttps://doi.org/10.1055/s-0040-1719874openalex-snapshot
Cascade Reaction of 3-Phenacylideneoxindoles with Trimethylsilyl Cyanide: Synthesis of Furan-Fused 1,3-Benzodiazepin-2-one Derivatives
inferred← citeshttps://doi.org/10.1080/00304948.2014.922378openalex-snapshot
Recent Developments in the Synthesis and Applications of Isatins
inferred← citeshttps://doi.org/10.1080/00397911.2014.891239openalex-snapshot
Novel 4-Aryl-2-amino-6-(naphthalene-1-yl)-3-cyanopyridine Derivates as Potential Organic Fluorescent Materials Prepared Under Microwave Irradiation via Three-Component Domino Reactions
inferred← citeshttps://doi.org/10.1080/00397911.2018.1525740openalex-snapshot
Catalyst-free synthesis of 3-substituted-3-hydroxy-2-oxindoles by reaction of isatin and cyclic enaminone in water
inferred← citeshttps://doi.org/10.2139/ssrn.4900393openalex-snapshot
Regioselective Synthesis of Functionalized Cyclopent-2-Enone-Derived Carbonylureas and Enaminohydroxybarbiturates from Alloxans in Water
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