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Silver-catalyzed decarboxylative acylation of quinoxalin-2(1H)-ones with α-oxo-carboxylic acids
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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/adsc.201400662openalex-snapshot
Assisted Tandem Palladium(II)/Palladium(0)‐Catalyzed C‐ and N‐Arylations of Quinoxalin‐2(1 H )‐ones in Water
inferredcites →https://doi.org/10.1002/adsc.201700070openalex-snapshot
Transition Metal‐Free Iodosobenzene‐Promoted Direct Oxidative 3‐Arylation of Quinoxalin‐2( H )‐ones with Arylhydrazines
inferredcites →https://doi.org/10.1002/chem.201604496openalex-snapshot
Decarboxylation as the Key Step in C−C Bond‐Forming Reactions
inferredcites →https://doi.org/10.1002/ejoc.201600754openalex-snapshot
Silver‐Promoted Cascade Reaction of 4‐Hydroxycoumarins with α‐Keto Acids under Microwave Irradiation: One‐Step Construction of Quaternary Stereocenters
inferredcites →https://doi.org/10.1002/jhet.5570430304openalex-snapshot
Novel 3‐benzoyl‐2‐piperazinylquinoxaline derivatives as potential antitumor agents
inferredcites →https://doi.org/10.1007/s11178-005-0210-2openalex-snapshot
Synthesis and Functionalization of 3-Ethylquinoxalin-2(1H)-one
inferredcites →https://doi.org/10.1016/b978-0-08-099406-2.00001-7openalex-snapshot
Progress in Quinoxaline Synthesis (Part 2)
inferredcites →https://doi.org/10.1016/j.tet.2014.12.029openalex-snapshot
Diacylation of coumarins by silver-catalyzed decarboxylative cross-coupling
inferredcites →https://doi.org/10.1016/j.tet.2014.12.095openalex-snapshot
Palladium-catalyzed decarboxylative C3-acylation of benzofurans and benzothiophenes with α-oxocarboxylic acids via direct sp2 C–H bond activation
inferredcites →https://doi.org/10.1016/s0040-4020(01)97768-3openalex-snapshot
Nucleophilic character of alkyl radicals—VI
inferredcites →https://doi.org/10.1021/acs.chemrev.6b00516openalex-snapshot
Metal-Catalyzed Decarboxylative C–H Functionalization
inferredcites →https://doi.org/10.1021/acs.joc.5b01450openalex-snapshot
Cobalt-Catalyzed Decarboxylative 2-Benzoylation of Oxazoles and Thiazoles with α-Oxocarboxylic Acids
inferredcites →https://doi.org/10.1021/acs.orglett.7b00310openalex-snapshot
Transition-Metal-Free Direct C–H Arylation of Quinoxalin-2(1 H )-ones with Diaryliodonium Salts at Room Temperature
inferredcites →https://doi.org/10.1021/jo501526aopenalex-snapshot
Reaction for the Synthesis of Benzimidazol-2-ones, Imidazo[5,4-b]-, and Imidazo[4,5-c]pyridin-2-ones via the Rearrangement of Quinoxalin-2-ones and Their Aza Analogues When Exposed to Enamines
inferredcites →https://doi.org/10.1021/jo502135dopenalex-snapshot
Rearrangement of Quinoxalin-2-ones When Exposed to Enamines Generated in Situ from Ketones and Ammonium Acetate: Method for the Synthesis of 1-(Pyrrolyl)benzimidazolones
inferredcites →https://doi.org/10.1021/ol301801ropenalex-snapshot
Decarboxylative Acylation of Cyclic Enamides with α-Oxocarboxylic Acids by Palladium-Catalyzed C–H Activation at Room Temperature
inferredcites →https://doi.org/10.1021/ol4028946openalex-snapshot
Palladium(II)-Catalyzed Oxidative Arylation of Quinoxalin-2(1 H )-ones with Arylboronic Acids
inferredcites →https://doi.org/10.1023/a:1022601829731openalex-snapshot
The Kornblum Reaction of α-Substituted 3-Benzyl-1,2-dihydro-2-oxoquinoxalines. Synthesis and Structure of 3-Benzoyl-2-oxo-1,2-dihydroquinoxaline
inferredcites →https://doi.org/10.1023/b:rucb.0000024846.27508.76openalex-snapshot
Ring contraction in reactions of 3-benzoylquinoxalin-2-ones with 1,2-phenylenediamines. Quinoxaline-benzoimidazole rearrangement
inferredcites →https://doi.org/10.1039/c1cs15093fopenalex-snapshot
Decarboxylative coupling reactions: a modern strategy for C–C-bond formation
inferredcites →https://doi.org/10.1039/c3cc40389kopenalex-snapshot
Copper-promoted decarboxylative direct C3-acylation of N-substituted indoles with α-oxocarboxylic acids
inferredcites →https://doi.org/10.1039/c3cc40709hopenalex-snapshot
Palladium-catalyzed decarboxylative C2-acylation of indoles with α-oxocarboxylic acids
inferredcites →https://doi.org/10.1039/c3ob42171fopenalex-snapshot
Copper-catalyzed decarboxylative C3-acylation of free (N–H) indoles with α-oxocarboxylic acids
inferredcites →https://doi.org/10.1039/c5cc08049eopenalex-snapshot
Direct phosphonation of quinoxalin-2(1H)-ones under transition-metal-free conditions
inferredcites →https://doi.org/10.1039/c6ob01283copenalex-snapshot
Copper-catalysed oxidative amination of quinoxalin-2(1H)-ones with aliphatic amines
inferredcites →https://doi.org/10.1039/c6ra03907copenalex-snapshot
Recent advances in the synthesis of benzimidazol(on)es via rearrangements of quinoxalin(on)es
inferredcites →https://doi.org/10.1039/c7ob00205jopenalex-snapshot
Metal-free oxidative ring contraction of benzodiazepinones: an entry to quinoxalinones
inferredcites →https://doi.org/10.1073/pnas.0704384105openalex-snapshot
Discovery of potent pteridine reductase inhibitors to guide antiparasite drug development
inferredcites →https://doi.org/10.1080/00397910802369554openalex-snapshot
Synthesis of Arylglyoxylic Acids and Their Collision-Induced Dissociation
inferredcites →https://doi.org/10.1134/s107042800610023xopenalex-snapshot
Oxidative dehydrobromination of 3-(α-bromobenzyl)quinoxalin-2(1H)-ones according to Kornblum as a simple and efficient synthetic route to quinoxalyl aryl ketones
inferredcites →https://doi.org/10.1155/2014/563406openalex-snapshot
Pharmacological Profile of Quinoxalinone
inferredcites →https://doi.org/10.1358/dof.2006.031.11.1037128openalex-snapshot
Recent advances in the research of quinoxalinone derivatives
inferredcites →https://doi.org/10.2174/138955706778742713openalex-snapshot
Chemistry, Biological Properties and SAR Analysis of Quinoxalinones
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/adsc.201800863openalex-snapshot
Direct C−H Trifluoromethylation of Quinoxalin‐2(1H)‐ones under Transition‐Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1002/adsc.201801076openalex-snapshot
[3+2] Cyclization of Azidotrimethylsilane with Quinoxalin‐2(1H)‐Ones to Synthesize Tetrazolo[1,5‐a]quinoxalin‐4(5H)‐Ones
inferred← citeshttps://doi.org/10.1002/adsc.201801661openalex-snapshot
Direct C(sp2)−H Amination to Synthesize Primary 3‐aminoquinoxalin‐2(1H)‐ones under Simple and Mild Conditions
inferred← citeshttps://doi.org/10.1002/adsc.201900066openalex-snapshot
Copper‐Catalyzed C3−H Difluoroacetylation of Quinoxalinones with Ethyl Bromodifluoroacetate
inferred← citeshttps://doi.org/10.1002/adsc.201900572openalex-snapshot
Visible Light‐Induced Regioselective Decarboxylative Alkylation of the C(sp2)−H Bonds of Non‐Aromatic Heterocycles
inferred← citeshttps://doi.org/10.1002/adsc.201900732openalex-snapshot
Visible‐Light‐Induced Alkoxylation of Quinoxalin‐2(1H)‐ones with Alcohols for the Synthesis of Heteroaryl Ethers
inferred← citeshttps://doi.org/10.1002/adsc.201900885openalex-snapshot
Visible Light‐Induced Photocatalytic C−H Perfluoroalkylation of Quinoxalinones under Aerobic Oxidation Condition
inferred← citeshttps://doi.org/10.1002/adsc.201901008openalex-snapshot
(Thio)etherification of Quinoxalinones under Visible‐Light Photoredox Catalysis
inferred← citeshttps://doi.org/10.1002/adsc.201901163openalex-snapshot
Metal‐Free C3 Hydroxylation of Quinoxalin‐2(1H)‐ones in Water
inferred← citeshttps://doi.org/10.1002/adsc.201901212openalex-snapshot
Metal Free Benzylation and Alkylation of Quinoxalin‐2(1H)‐ones with Alkenes Triggered by Sulfonyl Radical Generated from Sulfinic Acids
inferred← citeshttps://doi.org/10.1002/adsc.201901314openalex-snapshot
Hypervalent Iodine(III)‐Promoted Rapid Cascade Reaction of Quinoxalinones with Unactivated Alkenes and TMSN3
inferred← citeshttps://doi.org/10.1002/adsc.202000116openalex-snapshot
Photoredox Catalyst Free, Visible Light‐Promoted C3−H Acylation of Quinoxalin‐2(1H)‐ones in Water
inferred← citeshttps://doi.org/10.1002/adsc.202001182openalex-snapshot
Copper‐Catalyzed Regio‐ and Stereoselective Oxidative Vinylsulfonylation of Quinoxalinones with Alkynes and Sulfonyl Hydrazides
inferred← citeshttps://doi.org/10.1002/adsc.202001396openalex-snapshot
Visible‐Light‐Promoted Switchable Synthesis of C‐3‐Functionalized Quinoxalin‐2(1H)‐ones
inferred← citeshttps://doi.org/10.1002/adsc.202201241openalex-snapshot
Electrochemical Hydroalkylation of Quinoxalin‐2(1H)‐ones with Alkyl Halides
inferred← citeshttps://doi.org/10.1002/adsc.202301521openalex-snapshot
Visible Light‐Enabled Decarboxylative Alkylation of Quinoxalin‐2(1H)‐ones using Alkyl Carboxylic Acids via Energy Transfer Process
inferred← citeshttps://doi.org/10.1002/ajoc.201900118openalex-snapshot
Phenyliodonium Diacetate Mediated Carbotrifluoromethylation of Quinoxalin‐2(1H)‐ones
inferred← citeshttps://doi.org/10.1002/ajoc.201900369openalex-snapshot
Merging Visible‐Light Photoredox and Organoamine Catalysis for the C‐3 Difluoroalkylation of Quinoxalin‐2(1 H )‐Ones
inferred← citeshttps://doi.org/10.1002/ajoc.201900414openalex-snapshot
Visible‐Light‐Induced Trifluoromethylation of Quinoxalin‐2(1H)‐Ones under Photocatalyst‐Free Conditions
inferred← citeshttps://doi.org/10.1002/ajoc.201900484openalex-snapshot
Electrochemically Facilitated Oxidative Coupling of Quinoxalin‐2(1H)‐Ones with Diarylphosphine Oxides and Pyrroles: A Green Protocol for C−P, C−C(sp2) Bond Formation
inferred← citeshttps://doi.org/10.1002/ajoc.201900758openalex-snapshot
Transition‐Metal‐Free Radical C−H Methylation of Quinoxalinones with TBHP
inferred← citeshttps://doi.org/10.1002/ajoc.202000073openalex-snapshot
Photo‐Mediated Decarboxylative Cross Coupling of Quinoxalin‐2(1H)‐ones with Aliphatic Carboxylic Acids in Aqueous Solution: Synthesis of Alkylated Quinoxalin‐2(1H)‐ones and Preliminary Antifungal Evaluation Against Magnaporthe Grisea
inferred← citeshttps://doi.org/10.1002/ajoc.202000523openalex-snapshot
Copper‐Catalyzed Direct Oxidative Aroylations of Quinoxalinones with Methylarenes
inferred← citeshttps://doi.org/10.1002/ajoc.202000583openalex-snapshot
Copper‐Catalyzed Decarboxylative Reductive Sulfonylation of α‐Oxocarboxylic Acids with Aryl Sulfonyl Hydrazines
inferred← citeshttps://doi.org/10.1002/ajoc.202200453openalex-snapshot
Divergent Auto‐oxidative Alkylation and Alkanoacylation of Quinoxalin‐2(1H)‐ones with Aliphatic Aldehydes
inferred← citeshttps://doi.org/10.1002/ajoc.70463openalex-snapshot
NIS‐Mediated Olefination of Quinoxalin‐2(1 H )‐Ones Using Ketone Derivatives: A Facile Synthetic Access to ( Z )‐Enaminone Frameworks
inferred← citeshttps://doi.org/10.1002/aoc.7821openalex-snapshot
Fe 2 O 3 Nano‐Catalyst Mediated Oxidative Decarboxylation CH Acylation/Benzoylation of 3‐Alkylidene‐2‐Oxindoles With α‐Keto Acids
inferred← citeshttps://doi.org/10.1002/asia.202000916openalex-snapshot
Direct Introduction of Sulfonamide Groups into Quinoxalin‐2(1H)‐ones by Cu‐Catalyzed C3‐H Functionalization
inferred← citeshttps://doi.org/10.1002/asia.202201117openalex-snapshot
Transition‐metal‐free Synthesis of tetra‐substituted Vinyl Iodides by Cascade Sequential Reaction of α‐Keto Acids, 1‐Iodoalkynes, and Alkyl Halides
inferred← citeshttps://doi.org/10.1002/cctc.202000459openalex-snapshot
Visible‐Light Photoredox Catalyzed C−N Coupling of Quinoxaline‐2(1H)‐ones with Azoles without External Photosensitizer
inferred← citeshttps://doi.org/10.1002/cctc.202001691openalex-snapshot
Silver in C(sp2)‐H Functionalization
inferred← citeshttps://doi.org/10.1002/cctc.202400675openalex-snapshot
Visible‐Light‐Driven Heterocyclic Fluoroalkylation Via Electron Donor−Acceptor Complexes
inferred← citeshttps://doi.org/10.1002/chem.202400237openalex-snapshot
Electron Donor‐Acceptor Complex Driven Photocatalyst‐Free Trifluoromethylation of Heterocycles
inferred← citeshttps://doi.org/10.1002/ejoc.201800697openalex-snapshot
Copper‐Catalyzed Direct C‐3 Benzylation of Quinoxalin‐2(1H)‐ones with Methylarenes under Microwave Irradiation
inferred← citeshttps://doi.org/10.1002/ejoc.201901266openalex-snapshot
A Catalyst‐Free Minisci‐Type Reaction: the C–H Alkylation of Quinoxalinones with Sodium Alkylsulfinates and Phenyliodine(III) Dicarboxylates
inferred← citeshttps://doi.org/10.1002/ejoc.201901858openalex-snapshot
Copper‐Catalyzed Direct Carbamoylation of Quinoxalin‐2(1H)‐ones with Hydrazinecarboxamides Under Mild Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.202100269openalex-snapshot
Metal‐Free Direct Oxidative C−N Bond Coupling of Quinoxalin‐2(1H)‐ones with Azoles under Mild Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.202100348openalex-snapshot
Electrochemical Oxidative C−H Cyanation of Quinoxalin‐2(1H)‐ones with TMSCN
inferred← citeshttps://doi.org/10.1002/ejoc.202100896openalex-snapshot
Direct Difluoromethylation of Heterocycles through Photosensitized Electron Transfer
inferred← citeshttps://doi.org/10.1002/ejoc.202300752openalex-snapshot
Three‐Component Reactions of Quinoxalin‐2(1H)‐ones: Recent Advances
inferred← citeshttps://doi.org/10.1002/ejoc.202400162openalex-snapshot
Photo‐Induced Cross‐Dehydrogenative Coupling of Quinoxalin‐2(1H)‐ones with Aldehydes under Metal Free Conditions without an External Photocatalyst
inferred← citeshttps://doi.org/10.1002/ejoc.202401206openalex-snapshot
Photochemical‐, Electrochemical‐, and Photoelectrochemical‐ Catalyzed Hydrogen Atom Transfer from Aldehydes to Acyl Radicals and Their Transformations
inferred← citeshttps://doi.org/10.1002/jhet.70160openalex-snapshot
Ag‐Catalyzed Selective C1 ‐Acylation of Pyrrolo[1,2‐ a ]Quinoxalines With 2‐Oxo‐2‐Arylacetic Acids
inferred← citeshttps://doi.org/10.1002/slct.202103693openalex-snapshot
A CF 3 SO 2 Na‐Mediated Photocatalytic Strategy for Aerobic C3‐H Fluoroalkoxylation of Quinoxalinones with Fluoroalkyl Alcohols
inferred← citeshttps://doi.org/10.1002/slct.202201541openalex-snapshot
K 2 S 2 O 8 Mediated Three‐component Radical Cascade C3 Alkylation of Quinoxalin‐2(1 H )‐ones with Vinylarenes and 4‐Hydroxycoumarins/4‐Hydroxy‐6‐methyl‐2‐pyrone
inferred← citeshttps://doi.org/10.1002/slct.202203597openalex-snapshot
Metal‐ And Light‐Free Direct C‐3 Ketoalkylation of Quinoxalin‐2(1 H )‐Ones with Cyclopropanols in Aqueous Medium
inferred← citeshttps://doi.org/10.1002/slct.202203959openalex-snapshot
Hypervalent iodine mediated Pd(II)‐catalyzed ortho ‐C( sp 2 −H) functionalization of azoles deciphering Hantzsch ester and malononitrile as the functional group surrogates
inferred← citeshttps://doi.org/10.1002/slct.202303845openalex-snapshot
Iodine and DMSO as Surrogate of Hazardous Metal and Non‐Metal Reagents in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/slct.202502794openalex-snapshot
Silver‐Catalyzed Synthesis of N ‐Benzyl Sulfonamides via Sulfonamidation of Benzylic C(sp 3 )─H Bonds
inferred← citeshttps://doi.org/10.1007/s11426-018-9446-1openalex-snapshot
Metal-free C3-alkoxycarbonylation of quinoxalin-2(1H)-ones with carbazates as ecofriendly ester sources
inferred← citeshttps://doi.org/10.1016/b978-0-12-824285-8.00001-7openalex-snapshot
Applications of 2-Oxoacids
inferred← citeshttps://doi.org/10.1016/j.cclet.2020.11.034openalex-snapshot
Visible-light-induced three-component reaction of quinoxalin-2(1H)-ones, alkenes and CF3SO2Na leading to 3-trifluoroalkylated quinoxalin-2(1H)-ones
inferred← citeshttps://doi.org/10.1016/j.cclet.2021.04.016openalex-snapshot
Rapid alkenylation of quinoxalin-2(1H)-ones enabled by the sequential Mannich-type reaction and solar photocatalysis
inferred← citeshttps://doi.org/10.1016/j.cclet.2021.06.005openalex-snapshot
Visible-light-induced chemoselective reactions of quinoxalin-2(1H)-ones with alkylboronic acids under air/N2 atmosphere
inferred← citeshttps://doi.org/10.1016/j.comptc.2019.112639openalex-snapshot
Mechanisms of visible-light-induced Csp2-H functionalization of 1-methylquinoxalin-2(1H)-one and tetrahydrofuran: A DFT investigation
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132217openalex-snapshot
Visible-light induced direct C-H difluoromethylation of quinoxalin-2(1H)-ones by [bis(difluoroacetoxy)iodo]benzene under catalysis-free conditions
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132466openalex-snapshot
Direct Csp2−H difluoromethylation of heterocycle by K2S2O8
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134674openalex-snapshot
Visible-light-promoted oxidative decarboxylative acylation of acenaphthenone-2-ylidene ketones with α-keto carboxylic acids under metal, additonal oxidant and base-free condition
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.10.015openalex-snapshot
A simple and efficient method for the synthesis of 5,6-dihydropyrazin-2(1H)-one O-(tert-butyl)oximes, quinoxalin-2(1H)-one O-(tert-butyl)oximes and its derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.06.059openalex-snapshot
Visible-light-driven cyanoalkylation of quinoxalinones using cyclobutanone oxime esters as the radical precursors
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152691openalex-snapshot
Ag-catalyzed decarboxylative acylation of pyridazines using α-keto acids in aqueous media
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.152915openalex-snapshot
Eosin Y as a direct hydrogen-atom transfer photocatalyst for the C3-H acylation of quinoxalin-2(1H)-ones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153268openalex-snapshot
Intramolecular oxidative rearrangement: I2/TBHP/DMSO-mediated metal free facile access to quinoxalinone derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153439openalex-snapshot
Metal-free C3 α-aminoalkylation of quinoxalin-2(1H)-ones with amines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153550openalex-snapshot
The silver-mediated annulation of arylcarbamic acids and nitrosoarenes toward phenazines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153595openalex-snapshot
Photocatalyst-free visible light induced decarboxylative alkylation of quinoxalin-2(1H)-ones with carboxylic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.154913openalex-snapshot
Selective C–H acylation of quinolin-2(1H)-one with α-oxocarboxylic acids at the C3 position by sliver catalysis and its application in the synthesis of palbociclib
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.155363openalex-snapshot
Photochemical direct C3 cyanoalkylation of quinoxalin-2(1H)-ones with cyclobutanone oxime esters under catalyst-free conditions
inferred← citeshttps://doi.org/10.1016/s1872-2067(19)63526-6openalex-snapshot
C(sp2)–H/O–H cross-dehydrogenative coupling of quinoxalin-2(1H)-ones with alcohols under visible-light photoredox catalysis
inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00782openalex-snapshot
α-Keto Acids: Acylating Agents in Organic Synthesis
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01818openalex-snapshot
Photocatalytic Hydroacylation of Alkenes by Directly Using Acyl Oximes
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00043openalex-snapshot
Electrochemical Oxidative C–H Arylation of Quinoxalin(on)es with Arylhydrazine Hydrochlorides under Mild Conditions
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01626openalex-snapshot
Divergent Synthesis of 3-(Indol-2-yl)quinoxalin-2-ones and 4-(Benzimidazol-2-yl)-3-methyl(aryl)cinnolines via Polyphosphoric Acid (PPA)-Mediated Intramolecular Rearrangements of 3-(Methyl/aryl(2-phenylhydrazono)methyl)quinoxalin-2-ones
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02781openalex-snapshot
Photoinduced Dehydrogenative Amination of Quinoxalin-2(1H)-ones with Air as an Oxidant
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00631openalex-snapshot
Self-Catalyzed, Visible-Light-Induced Selective C3–H Aroylation of Quinoxalin-2(1 H )-ones with Arylaldehydes by Air as an Oxidant
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01957openalex-snapshot
Pd-Catalyzed Photochemical Reductive Alkylation of Quinoxalinones and Dibenzoxazepines
inferred← citeshttps://doi.org/10.1021/acs.joc.6c01075openalex-snapshot
K2S2O8–Promoted C3-Bromination of Heteroarenes with Sodium Bromide
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02947openalex-snapshot
Gold(III)-Catalyzed Decarboxylative C3-Benzylation of Indole-3-carboxylic Acids with Benzylic Alcohols in Water
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00657openalex-snapshot
Metal-Free Direct C–H Cyanoalkylation of Quinoxalin-2(1H)-Ones by Organic Photoredox Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01181openalex-snapshot
Direct C3 Alkoxylation of Quinoxalin-2(1H)-ones with Alcohols via Cross-Dehydrogenative Coupling under Catalyst-Free Conditions
inferred← citeshttps://doi.org/10.1021/acs.joc.9b03505openalex-snapshot
Metal-Free Trifluoroalkylation of Quinoxalin-2(1H)-ones with Unactivated Alkenes and Langlois’ Reagent
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01588openalex-snapshot
Ag-Catalyzed Oxidative ipso-Cyclization via Decarboxylative Acylation/Alkylation: Access to 3-Acyl/Alkyl-spiro[4.5]trienones
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02518openalex-snapshot
Arylaminomethyl Radical-Initiated Cascade Annulation Reaction of Quinoxalin-2(1H)-ones Catalyzed by Recyclable Photocatalyst Perovskite
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01977openalex-snapshot
Discovery of the Quinoxalinone–B(C 6 F 5 ) 3 ·H 2 O Combo as a Photocatalyst by Acidochromism Strategy: Aerobic Oxidation of Alcohol, Alkene, and Thiols
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02296openalex-snapshot
Visible Light-Induced Electron–Donor–Acceptor-Mediated C-3 Coupling of Quinoxalin-2(1 H )-ones with Unactivated Aryl Iodides
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02316openalex-snapshot
Visible-Light-Induced Photocatalytic Deoxygenative Benzylation of Quinoxalin-2-(1H)-ones with Carboxylic Acid Anhydrides
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c00440openalex-snapshot
Decarboxylative and Deoxygenative/Decarbonylative Alkylation of Heterocycles with α-Keto Acids
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03984openalex-snapshot
Direct C–H Cyanoalkylation of Quinoxalin-2(1H)-ones via Radical C–C Bond Cleavage
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03079openalex-snapshot
Metal-Free C(sp2)–H/N–H Cross-Dehydrogenative Coupling of Quinoxalinones with Aliphatic Amines under Visible-Light Photoredox Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03865openalex-snapshot
Iminyl Radical-Triggered Intermolecular Distal C(sp3)–H Heteroarylation via 1,5-Hydrogen-Atom Transfer (HAT) Cascade
inferred← citeshttps://doi.org/10.1021/acssuschemeng.0c02289openalex-snapshot
Divergent g-C3N4-catalyzed Reactions of Quinoxalin-2(1H)-ones with N-Aryl Glycines under Visible Light: Solvent-Controlled Hydroaminomethylation and Annulation
inferred← citeshttps://doi.org/10.1021/acssuschemeng.2c04720openalex-snapshot
Piezocatalyzed Decarboxylative Acylation of Quinoxalin-2(1 H )-ones Using Ball Milling
inferred← citeshttps://doi.org/10.1021/acssuschemeng.8b04652openalex-snapshot
Metal-Free Visible-Light-Induced C–H/C–H Cross-Dehydrogenative-Coupling of Quinoxalin-2(H)-ones with Simple Ethers
inferred← citeshttps://doi.org/10.1021/acssuschemeng.9b05715openalex-snapshot
Visible-Light-Initiated Cross-Dehydrogenative Coupling of Quinoxalin-2(1H)-ones and Simple Amides with Air as an Oxidant
inferred← citeshttps://doi.org/10.1039/c8ob00206aopenalex-snapshot
Metal-free oxidative coupling of quinoxalin-2(1 H )-ones with arylaldehydes leading to 3-acylated quinoxalin-2(1 H )-ones
inferred← citeshttps://doi.org/10.1039/c8ob00375kopenalex-snapshot
Persulfate-promoted oxidative C–N bond coupling of quinoxalinones and NH -sulfoximines
inferred← citeshttps://doi.org/10.1039/c8qo00328aopenalex-snapshot
Metal-free direct oxidative C–C bond coupling of pyrazolones and quinoxalinones
inferred← citeshttps://doi.org/10.1039/c8qo00731dopenalex-snapshot
Transition-metal-free direct C-3 alkylation of quinoxalin-2(1 H )-ones with ethers
inferred← citeshttps://doi.org/10.1039/c8qo00979aopenalex-snapshot
Copper-catalyzed oxidative coupling of quinoxalin-2(1 H )-ones with alcohols: access to hydroxyalkylation of quinoxalin-2(1 H )-ones
inferred← citeshttps://doi.org/10.1039/c8qo01127copenalex-snapshot
Selective synthesis of aryl thioamides and aryl-α-ketoamides from α-oxocarboxylic acids and tetraalkylthiuram disulfides: an unexpected chemoselectivity from aryl sulfonyl chlorides
inferred← citeshttps://doi.org/10.1039/c8ra03259aopenalex-snapshot
Visible-light-induced C(sp 3 )–H activation for a C–C bond forming reaction of 3,4-dihydroquinoxalin-2(1 H )-one with nucleophiles using oxygen with a photoredox catalyst or under catalyst-free conditions
inferred← citeshttps://doi.org/10.1039/c9gc02662bopenalex-snapshot
A niobium-catalyzed coupling reaction of α-keto acids with ortho -phenylenediamines: synthesis of 3-arylquinoxalin-2(1 H )-ones
inferred← citeshttps://doi.org/10.1039/c9gc03045jopenalex-snapshot
Direct C–H sulfenylation of quinoxalinones with thiols under visible-light-induced photocatalyst-free conditions
inferred← citeshttps://doi.org/10.1039/c9gc03899jopenalex-snapshot
Visible-light-induced decarboxylative acylation of quinoxalin-2(1 H )-ones with α-oxo carboxylic acids under metal-, strong oxidant- and external photocatalyst-free conditions
inferred← citeshttps://doi.org/10.1039/c9ob00294dopenalex-snapshot
Copper-catalyzed C–H/N–H cross-coupling reactions for the synthesis of 3-heteroaryl quinoxalin-2(1 H )-ones
inferred← citeshttps://doi.org/10.1039/c9ob00782bopenalex-snapshot
Recent advances in the direct functionalization of quinoxalin-2(1 H )-ones
inferred← citeshttps://doi.org/10.1039/c9ob01169bopenalex-snapshot
Visible-light induced decarboxylative alkylation of quinoxalin-2(1 H )-ones at the C3-position
inferred← citeshttps://doi.org/10.1039/c9qo00063aopenalex-snapshot
Highly efficient copper-catalyzed direct C–H amidation of quinoxalin-2(1 H )-ones with amidates under microwave irradiation
inferred← citeshttps://doi.org/10.1039/c9qo00105kopenalex-snapshot
Transition-metal-free decarboxylative C3-difluoroarylmethylation of quinoxalin-2(1 H )-ones with α,α-difluoroarylacetic acids
inferred← citeshttps://doi.org/10.1039/c9qo00625gopenalex-snapshot
Ring-opening C(sp 3 )–C coupling of cyclobutanone oxime esters for the preparation of cyanoalkyl containing heterocycles enabled by photocatalysis
inferred← citeshttps://doi.org/10.1039/c9qo01055fopenalex-snapshot
Transition-metal-free direct C-3 cyanation of quinoxalin-2(1 H )-ones with ammonium thiocyanate as the “CN” source
inferred← citeshttps://doi.org/10.1039/c9qo01240kopenalex-snapshot
Visible-light-promoted direct C–H/S–H cross-coupling of quinoxalin-2(1 H )-ones with thiols leading to 3-sulfenylated quinoxalin-2(1 H )-ones in air
inferred← citeshttps://doi.org/10.1039/c9qo01322aopenalex-snapshot
Transition-metal free direct C–H functionalization of quinoxalin-2(1 H )-ones with oxamic acids leading to 3-carbamoyl quinoxalin-2(1 H )-ones
inferred← citeshttps://doi.org/10.1039/c9qo01334bopenalex-snapshot
Visible-light-promoted acridine red catalyzed aerobic oxidative decarboxylative acylation of α-oxo-carboxylic acids with quinoxalin-2(1 H )-ones
inferred← citeshttps://doi.org/10.1039/c9ra10194bopenalex-snapshot
Visible-light-induced aerobic C3–H fluoroalkoxylation of quinoxalin-2(1 H )-ones with fluoroalkyl alcohols
inferred← citeshttps://doi.org/10.1039/d0gc02844dopenalex-snapshot
Aryl acyl peroxides for visible-light induced decarboxylative arylation of quinoxalin-2(1 H )-ones under additive-, metal catalyst-, and external photosensitizer-free and ambient conditions
inferred← citeshttps://doi.org/10.1039/d0ob00055hopenalex-snapshot
A silver-catalyzed radical ring-opening reaction of cyclopropanols with sulfonyl oxime ethers
inferred← citeshttps://doi.org/10.1039/d0ob01304hopenalex-snapshot
tert -Butylhydroperoxide (TBHP) mediated oxidative cross-dehydrogenative coupling of quinoxalin-2(1 H )-ones with 4-hydroxycoumarins, 4-hydroxy-6-methyl-2-pyrone and 2-hydroxy-1,4-naphthoquinone under metal-free conditions
inferred← citeshttps://doi.org/10.1039/d0ob01423kopenalex-snapshot
Metal-free C3–H acylation of quinoxalin-2(1 H )-ones with α-oxo-carboxylic acids
inferred← citeshttps://doi.org/10.1039/d0ob01570aopenalex-snapshot
Silver-promoted oxidative sulfonylation and ring-expansion of vinylcyclopropanes with sodium sulfinates leading to dihydronaphthalene derivatives
inferred← citeshttps://doi.org/10.1039/d0ra02059aopenalex-snapshot
Photoinitiated decarboxylative C3-difluoroarylmethylation of quinoxalin-2(1 H )-ones with potassium 2,2-difluoro-2-arylacetates in water
inferred← citeshttps://doi.org/10.1039/d1nj04805hopenalex-snapshot
Visible-light-promoted/PIFA-mediated direct C–H acylation of quinoxalin-2(1 H )-ones with aldehydes
inferred← citeshttps://doi.org/10.1039/d1ob00156fopenalex-snapshot
K 2 S 2 O 8 -mediated regio- and stereo-selective thiocyanation of enamides with NH 4 SCN
inferred← citeshttps://doi.org/10.1039/d1ob00610jopenalex-snapshot
Ni-Catalyzed radical cyclization of vinyl azides with cyclobutanone oxime esters to access cyanoalkyl containing quinoxalin-2(1 H )-ones
inferred← citeshttps://doi.org/10.1039/d1ob00769fopenalex-snapshot
Unusual C 3 -acetylation of quinoxalin-2(1 H )-one via oxidative C–C and C–O bond cleavages of PEG-400
inferred← citeshttps://doi.org/10.1039/d1ob02015copenalex-snapshot
Metal-free regioselective nitration of quinoxalin-2(1 H )-ones with tert -butyl nitrite
inferred← citeshttps://doi.org/10.1039/d2cc06887gopenalex-snapshot
Radical-mediated remote migration of quinoxalinones
inferred← citeshttps://doi.org/10.1039/d2ob00744dopenalex-snapshot
Copper-catalyzed C-3 benzylation of quinoxalin-2(1 H )-ones with benzylsulfonyl hydrazides
inferred← citeshttps://doi.org/10.1039/d2ra00753copenalex-snapshot
Regioselective C-3-alkylation of quinoxalin-2(1 H )-ones via C–N bond cleavage of amine derived Katritzky salts enabled by continuous-flow photoredox catalysis
inferred← citeshttps://doi.org/10.1039/d2ra04546jopenalex-snapshot
BF 3 ·Et 2 O-Mediated annulation of α-keto acids with aliphatic ketones for the synthesis of γ-hydroxy-butenolides and γ-alkylidene-butenolides
inferred← citeshttps://doi.org/10.1039/d3ob00280bopenalex-snapshot
Oxidative cross-coupling of quinoxalinones with indoles enabled by acidochromism
inferred← citeshttps://doi.org/10.1039/d3ob00682dopenalex-snapshot
Recent advances in catalytic decarboxylative transformations of carboxylic acid groups attached to a non-aromatic sp 2 or sp carbon
inferred← citeshttps://doi.org/10.1039/d5ob00018aopenalex-snapshot
Visible light-induced g-C 3 N 4 catalyzed C–H acylation and trifluoromethylation of quinoxalinones: an efficient and recyclable approach
inferred← citeshttps://doi.org/10.1039/d5ob00308copenalex-snapshot
Recent advances in photo-promoted generalized C3–H alkylation of quinoxalin-2(1 H )-ones
inferred← citeshttps://doi.org/10.1039/d5ob01618eopenalex-snapshot
Metal- and photocatalyst-free C3–H functionalization of quinoxalin-2(1 H )-ones enabled by electron donor–acceptor complex photoactivation
inferred← citeshttps://doi.org/10.1039/d6ob00743kopenalex-snapshot
HBr as a dual functional catalyst enabling aerobic CDC coupling of quinoxalin-2(1 H )-ones with electron-rich heteroarenes
inferred← citeshttps://doi.org/10.1039/d6ob01048bopenalex-snapshot
Copper( ii )-catalyzed C3-acylation of quinoxalin-2(1 H )-ones with methyl ketones via the formal decarbonylation of 1,2-diketones
inferred← citeshttps://doi.org/10.1055/a-1780-1691openalex-snapshot
Reactions of α-Phenylglyoxylic Acids with ortho-Functionalized Anilines in Deep Eutectic Solvents: Selective Syntheses of 3-Aryl-2H-benzo[b][1,4]oxazin-2-ones, 2-Arylbenzothiazoles, and 3-Arylquinoxalin-2(1H)-ones
inferred← citeshttps://doi.org/10.1055/a-1815-3539openalex-snapshot
Copper-Catalyzed Alkylation of Quinoxalin-2(1H)-ones with Styrenes and tert-Butyl Peroxybenzoate
inferred← citeshttps://doi.org/10.1055/a-1899-5409openalex-snapshot
Visible-Light-Induced Recyclable g-C3N4 Catalyzed C–H Hydroxylation of Quinoxalin-2(1H)-ones
inferred← citeshttps://doi.org/10.1055/s-0037-1611910openalex-snapshot
Recent Developments in Direct C–H Functionalization of Quinoxalin-2(1H)-ones via Radical Addition Processes
inferred← citeshttps://doi.org/10.1080/00397911.2020.1765257openalex-snapshot
Recent advances and perspectives on the synthesis and C–H bond functionalization of quinoxalin-2(1H)-one
inferred← citeshttps://doi.org/10.1360/tb-2023-0360openalex-snapshot
Visible light promoted benzoylation of quinoxalinone-2(1H)-ones
inferred← citeshttps://doi.org/10.2174/1385272824999201230211157openalex-snapshot
Recent Advances in Minisci-type Reactions and Applications in Organic Synthesis
inferred← citeshttps://doi.org/10.3390/molecules27155044openalex-snapshot
Sunlight Induced and Recyclable g-C3N4 Catalyzed C-H Sulfenylation of Quinoxalin-2(1H)-Ones
inferred← citeshttps://doi.org/10.3390/molecules28135030openalex-snapshot
Recent Developments in Direct C–H Functionalization of Quinoxalin-2(1H)-Ones via Heterogeneous Catalysis Reactions
inferred← citeshttps://doi.org/10.3390/molecules28145342openalex-snapshot
Silver-Catalyzed Decarboxylative Acylation of Isocyanides Accesses to α-Ketoamides with Air as a Sole Oxidant
inferred← citeshttps://doi.org/10.3390/molecules31060959openalex-snapshot
Efficient Approaches to Six-Membered Polyazacyclic Compounds—Part 3: C—H Functionalization of Heterocycles
inferred← citeshttps://doi.org/10.6023/cjoc202108023openalex-snapshot
Electrochemical Oxidative C—H Trifluoromethylation of Quinoxalin-2(1H)-ones and the Performance Evaluation via Electro-descriptors
inferred← citeshttps://doi.org/10.6023/cjoc202401015openalex-snapshot
Recent Advances of Minisci Reactions in Aqueous Solution
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