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Employing Arynes in Transition-Metal-Free Monoarylation of Aromatic Tertiary Amines
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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/ajoc.201200142openalex-snapshot
A Closer Look at Aryne Chemistry: Details that Remain Mysterious
inferredcites →https://doi.org/10.1002/anie.200300594openalex-snapshot
Modern Synthetic Methods for Copper‐Mediated C(aryl)O, C(aryl)N, and C(aryl)S Bond Formation
inferredcites →https://doi.org/10.1002/anie.200490023openalex-snapshot
Modern Synthetic Methods for Copper‐Mediated C(aryl)O, C(aryl)N, and C(aryl)S Bond Formation
inferredcites →https://doi.org/10.1002/anie.200600291openalex-snapshot
Insertion of Arynes into σ Bonds
inferredcites →https://doi.org/10.1002/anie.200804497openalex-snapshot
Catalytic CC, CN, and CO Ullmann‐Type Coupling Reactions
inferredcites →https://doi.org/10.1002/anie.200901410openalex-snapshot
The Benzyne Aza‐Claisen Reaction
inferredcites →https://doi.org/10.1002/anie.201106150openalex-snapshot
Transition‐Metal‐Free Direct Arylation of Anilines
inferredcites →https://doi.org/10.1002/anie.201106984openalex-snapshot
Arynes in Transition‐Metal‐Free Multicomponent Coupling Reactions
inferredcites →https://doi.org/10.1002/anie.201107485openalex-snapshot
Arynes and Cyclohexyne in Natural Product Synthesis
inferredcites →https://doi.org/10.1002/anie.201203269openalex-snapshot
Beyond Directing Groups: Transition‐Metal‐Catalyzed CH Activation of Simple Arenes
inferredcites →https://doi.org/10.1002/anie.201300382openalex-snapshot
Transition‐Metal‐Free Amination of Aryl boronic Acids and Their Derivatives
inferredcites →https://doi.org/10.1002/anie.201302783openalex-snapshot
Synchronous ArF and ArSn Bond Formation through Fluorostannylation of Arynes
inferredcites →https://doi.org/10.1002/anie.201304278openalex-snapshot
Transition‐Metal‐Free Multicomponent Reactions Involving Arynes, N‐Heterocycles, and Isatins
inferredcites →https://doi.org/10.1016/j.tetlet.2010.11.103openalex-snapshot
Metal-free carbon–nitrogen bond-forming coupling reaction between arylboronic acids and organic azides
inferredcites →https://doi.org/10.1016/j.tetlet.2012.07.026openalex-snapshot
A C–N insertion of β-lactam to benzyne: unusual formation of acridone
inferredcites →https://doi.org/10.1021/ar800098popenalex-snapshot
Evolution of a Fourth Generation Catalyst for the Amination and Thioetherification of Aryl Halides
inferredcites →https://doi.org/10.1021/ar9600650openalex-snapshot
Rational Development of Practical Catalysts for Aromatic Carbon−Nitrogen Bond Formation
inferredcites →https://doi.org/10.1021/cr200478hopenalex-snapshot
A Comprehensive History of Arynes in Natural Product Total Synthesis
inferredcites →https://doi.org/10.1021/ja305448wopenalex-snapshot
Direct Stereospecific Amination of Alkyl and Aryl Pinacol Boronates
inferredcites →https://doi.org/10.1021/ja309637ropenalex-snapshot
Elusive Metal-Free Primary Amination of Arylboronic Acids: Synthetic Studies and Mechanism by Density Functional Theory
inferredcites →https://doi.org/10.1021/jo0602221openalex-snapshot
Facile N-Arylation of Amines and Sulfonamides and O-Arylation of Phenols and Arenecarboxylic Acids
inferredcites →https://doi.org/10.1021/jo3011073openalex-snapshot
Formation of Acridones by Ethylene Extrusion in the Reaction of Arynes with β-Lactams and Dihydroquinolinones
inferredcites →https://doi.org/10.1021/jo302378wopenalex-snapshot
Synthesis ofo-(Dimethylamino)aryl Ketones, Acridones, Acridinium Salts, and 1H-Indazoles by the Reaction of Hydrazones and Arynes
inferredcites →https://doi.org/10.1021/ol0358612openalex-snapshot
Facile N-Arylation of Amines and Sulfonamides
inferredcites →https://doi.org/10.1021/ol048298bopenalex-snapshot
A 2:1 Coupling Reaction of Arynes with Aldehydes via o-Quinone Methides: Straightforward Synthesis of 9-Arylxanthenes
inferredcites →https://doi.org/10.1021/ol301742kopenalex-snapshot
A Practical and General Diels–Alder Reaction of Pentafulvenes with Arynes
inferredcites →https://doi.org/10.1021/ol301912aopenalex-snapshot
Transition-Metal-Free Electrophilic Amination of Arylboroxines
inferredcites →https://doi.org/10.1021/ol302180vopenalex-snapshot
Transition-Metal-Free α-Arylation of β-Keto Amides via an Interrupted Insertion Reaction of Arynes
inferredcites →https://doi.org/10.1021/ol302997qopenalex-snapshot
Efficient Diels–Alder Reaction of 1,2-Benzoquinones with Arynes and Its Utility in One-Pot Reactions
inferredcites →https://doi.org/10.1021/ol400780fopenalex-snapshot
P-Arylation: Arynes to Aryl-Phosphonates, -Phosphinates, and -Phosphine Oxides
inferredcites →https://doi.org/10.1021/ol401518copenalex-snapshot
Insertion of Arynes into N-Halo Bonds: A Direct Approach to o-Haloaminoarenes
inferredcites →https://doi.org/10.1021/ol4023134openalex-snapshot
Multicomponent Reactions Involving Arynes, Quinolines, and Aldehydes
inferredcites →https://doi.org/10.1039/c1cs15082kopenalex-snapshot
Recent advances in the transition metal-catalyzed twofold oxidative C–H bond activation strategy for C–C and C–N bond formation
inferredcites →https://doi.org/10.1039/c2cc36128kopenalex-snapshot
Tandem carbon–carbon bond insertion and intramolecular aldol reaction of benzyne with aroylacetones: novel formation of 4,4′-disubstituted 1,1′-binaphthols
inferredcites →https://doi.org/10.1039/c2cs15310fopenalex-snapshot
Recent advances in transition-metal-free carbon–carbon and carbon–heteroatom bond-forming reactions using arynes
inferredcites →https://doi.org/10.1039/c2ob26673copenalex-snapshot
Use of benzynes for the synthesis of heterocycles
inferredcites →https://doi.org/10.1039/c3cc42854kopenalex-snapshot
Three-component reaction of small-ring cyclic amines with arynes and acetonitrile
inferredcites →https://doi.org/10.1055/s-0030-1258379openalex-snapshot
Copper-Promoted Carbon-Heteroatom Bond Cross-Coupling with Boronic Acids and Derivatives
inferredcites →https://doi.org/10.1055/s-0031-1289614openalex-snapshot
Non-Cyclizing Direct Transformation of Arene Carbon-Hydrogen Bonds into Carbon-Nitrogen Bonds
inferredcites →https://doi.org/10.1055/s-0031-1290401openalex-snapshot
Aryne Insertion Reactions into Carbon-Carbon σ-Bonds
inferredcites →https://doi.org/10.1055/s-2003-42473openalex-snapshot
Renaissance of Ullmann and Goldberg Reactions - Progress in Copper Catalyzed C-N-, C-O- and C-S-Coupling
inferredcites →https://doi.org/10.1080/00304940809458089openalex-snapshot
RECENT APPLICATIONS OF ARYNE CHEMISTRY TO ORGANIC SYNTHESIS. A REVIEW
inferredcites →https://doi.org/10.1246/bcsj.20090245openalex-snapshot
Aryne, ortho-Quinone Methide, and ortho-Quinodimethane: Synthesis of Multisubstituted Arenes Using the Aromatic Reactive Intermediates
inferredcites →https://doi.org/10.1246/bcsj.20100266openalex-snapshot
Reaction of Benzyne with Formamides and Acetylimidazole
inferredcites →https://doi.org/10.1246/cl.1983.1211openalex-snapshot
FLUORIDE-INDUCED 1,2-ELIMINATION OF O -TRIMETHYLSILYLPHENYL TRIFLATE TO BENZYNE UNDER MILD CONDITIONS
inferredcites →https://doi.org/10.3987/rev-11-724openalex-snapshot
Reaction of Arynes with Carbon-Heteroatom Double Bonds
inferredcites →https://doi.org/10.5860/choice.42-4660openalex-snapshot
Amines: synthesis, properties, and applications
inferredcites →https://doi.org/10.5860/choice.46-3849openalex-snapshot
Amino group chemistry: from synthesis to the life sciences
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.4766478openalex-extracted
An Experimental and Dft Study of the Reaction between Dichloroethylene Carbonate and Triethylamine in Dimethyl Carbonate
inferred← citeshttps://doi.org/10.1002/9783527823086.ch4openalex-snapshot
Recent Insertion Reactions of Aryne Intermediates
inferred← citeshttps://doi.org/10.1002/adsc.202000821openalex-snapshot
Iridium‐Catalysed Reductive Deoxygenation of Ketones with Formic Acid as Traceless Hydride Donor
inferred← citeshttps://doi.org/10.1002/ajoc.201700598openalex-snapshot
Benzyne‐Promoted Curtius‐Type Rearrangement of Acyl Hydrazides in the Presence of Nucleophiles
inferred← citeshttps://doi.org/10.1002/ange.201409141openalex-snapshot
Regioselective Insertion of o‐Carborynes into the α‐CH Bond of Tertiary Amines: Synthesis of α‐Carboranylated Amines
inferred← citeshttps://doi.org/10.1002/ange.201909213openalex-snapshot
Über bislang nicht beachtete Parallelen in der Reaktivität von Arinen und Donor‐Akzeptor‐Cyclopropanen
inferred← citeshttps://doi.org/10.1002/ange.202310583openalex-snapshot
Aryne‐Enabled C−N Arylation of Anilines
inferred← citeshttps://doi.org/10.1002/ange.202519628openalex-snapshot
Construction of Biaryl Skeletons Initiated with Benzyne Insertion into C═S Double Bond of Pyridine‐2(1 H )‐thiones
inferred← citeshttps://doi.org/10.1002/anie.201409141openalex-snapshot
Regioselective Insertion of o ‐Carborynes into the α‐CH Bond of Tertiary Amines: Synthesis of α‐Carboranylated Amines
inferred← citeshttps://doi.org/10.1002/anie.201909213openalex-snapshot
Uncovering the Neglected Similarities of Arynes and Donor–Acceptor Cyclopropanes
inferred← citeshttps://doi.org/10.1002/anie.202310583openalex-snapshot
Aryne‐Enabled C−N Arylation of Anilines
inferred← citeshttps://doi.org/10.1002/anie.202519628openalex-snapshot
Construction of Biaryl Skeletons Initiated with Benzyne Insertion into C═S Double Bond of Pyridine‐2(1 H )‐thiones
inferred← citeshttps://doi.org/10.1002/chem.202004356openalex-snapshot
Aromatic Aza‐Claisen Rearrangement of Arylpropargylammonium Salts Generated in situ from Arynes and Tertiary Propargylamines
inferred← citeshttps://doi.org/10.1002/chin.201413072openalex-snapshot
ChemInform Abstract: Employing Arynes in Transition‐Metal‐Free Monoarylation of Aromatic Tertiary Amines.
inferred← citeshttps://doi.org/10.1002/ejoc.201500456openalex-snapshot
2,2′‐Bis‐substituted Biphenyls by the Addition of Nucleophiles to Benzyne Followed by In Situ Oxidative Homocoupling
inferred← citeshttps://doi.org/10.1002/ejoc.201501503openalex-snapshot
Access to Atropisomerically Enriched Biaryls by the Coupling of Aryllithiums with Arynes under Control by Homochiral Oxazolines
inferred← citeshttps://doi.org/10.1002/ejoc.201600244openalex-snapshot
Tandem Reaction of Arynes with Tertiary Amines and Aldehydes: Formation of 9‐ and 10‐Membered Dibenzo[1,5]oxaza Heterocycles
inferred← citeshttps://doi.org/10.1002/ejoc.201900130openalex-snapshot
Transition‐Metal‐Free Heterobiaryl Synthesis via Aryne Coupling
inferred← citeshttps://doi.org/10.1002/slct.202102042openalex-snapshot
Transition Metal‐Free Sulfenylation of C−H Bonds for C−S Bond Formation in Recent Years: Mechanistic Approach and Promising Future
inferred← citeshttps://doi.org/10.1007/s10593-021-03005-2openalex-snapshot
Dehydrobenzene in the Reaction of a Tandem [4+2]/[4+2] Cycloaddition with Linear bis-furyldienes
inferred← citeshttps://doi.org/10.1016/b978-0-323-85153-4.00001-0openalex-snapshot
Molecular rearrangements
inferred← citeshttps://doi.org/10.1016/j.ccr.2015.07.011openalex-snapshot
Recent advances in the chemistry of carborynes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2024.123124openalex-snapshot
Application of indole-based monophosphine in ppm level Pd-catalyzed C–N bond formation
inferred← citeshttps://doi.org/10.1016/j.tet.2016.08.058openalex-snapshot
CoPc/Cu(OAc)2-catalyzed N-arylation of amines with arylhydrazines leading to N-aryl amines
inferred← citeshttps://doi.org/10.1016/j.tet.2018.11.065openalex-snapshot
Facile construction of three-membered rings via benzyne-promoted Darzens-type reaction of tertiary amines
inferred← citeshttps://doi.org/10.1016/j.tet.2026.135364openalex-snapshot
Tertiary amines as nitrogen surrogates in C–N bond formation: Recent advances and perspectives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.01.022openalex-snapshot
Transition-metal-free synthesis of aromatic amines via the reaction of benzynes with isocyanates
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.03.067openalex-snapshot
Direct arylation of tertiary amines via aryne intermediates using diaryliodonium salts
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151018openalex-snapshot
Transition-Metal-Free Diarylation of Isocyanates with Arynes
inferred← citeshttps://doi.org/10.1021/acs.accounts.6b00188openalex-snapshot
Employing Arynes in Diels–Alder Reactions and Transition-Metal-Free Multicomponent Coupling and Arylation Reactions
inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c01011openalex-snapshot
o -Silylaryl Triflates: A Journey of Kobayashi Aryne Precursors
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01667openalex-snapshot
Synthesis of Tetracyclic Benzoxazolo-indol-3-ones from Isatogens and Arynes through a [3 + 2]-Cycloaddition and Skeletal Reorganization
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02827openalex-snapshot
Reactions of Tröger’s Base Derivatives with Aryne Intermediates
inferred← citeshttps://doi.org/10.1021/acs.joc.5c03027openalex-snapshot
1 H -Isoindolynes: Arynes Accessible by a One-Pot, Ambient Temperature, Three-Component Cascade
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02296openalex-snapshot
Metal-Free Blue Dye Synthesis: Oxidative Coupling of Benzylamines and N,N-Dimethylanilines to Yield 4,4′-Diaminotriarylmethanes in the Presence of Salicylic Acid as a Co-oxidant
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01058openalex-snapshot
Three-Component Reactions of Arynes, Amines, and Nucleophiles via a One-Pot Process
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00090openalex-snapshot
Three-Component Coupling Reactions of Aryne, DMSO, and Activated Alkyne: Stereoselective Synthesis of 2-[(o-Methylthio)aryloxy]-Substituted Dialkyl Maleates
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00703openalex-snapshot
Palladium-Catalyzed C(sp2)–N Bond Cross-Coupling with Triaryl Phosphates
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c02662openalex-snapshot
Three-Component, Diastereoselective [6 + 3] Annulation of Tropone, Imino Esters, and Arynes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01704openalex-snapshot
The Aryne aza-Diels–Alder Reaction: Flexible Syntheses of Isoquinolines
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02804openalex-snapshot
Metal-Free Approach for the Synthesis of N-Aryl Sulfoximines via Aryne Intermediate
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03319openalex-snapshot
Three-Component Coupling Involving Arynes, Aromatic Tertiary Amines, and Aldehydes via Aryl–Aryl Amino Group Migration
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00078openalex-snapshot
N-Arylation of Tertiary Amines under Mild Conditions
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02344openalex-snapshot
Aryne-Mediated [2,3]-Sigmatropic Rearrangement of Tertiary Allylic Amines
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02809openalex-snapshot
The Aryne [2,3] Stevens Rearrangement
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02845openalex-snapshot
Substrate-Controlled Selectivity Switch in the Three-Component Coupling Involving Arynes, Aromatic Tertiary Amines, and CO 2
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00365openalex-snapshot
Stereospecific Nucleophilic Substitution of Enantioenriched Tertiary Benzylic Amines via in Situ Activation with Benzyne
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02888openalex-snapshot
Mechanistic Duality in Tertiary Amine Additions to Thermally Generated Hexadehydro-Diels–Alder Benzynes
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03458openalex-snapshot
Multiheterocyclic Motifs via Three-Component Reactions of Benzynes, Cyclic Amines, and Protic Nucleophiles
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03789openalex-snapshot
Three-Component Aminoselenation of Arynes
inferred← citeshttps://doi.org/10.1021/ol4033094openalex-snapshot
Efficient Synthesis of 9-Aryldihydrophenanthrenes by a Cascade Reaction Involving Arynes and Styrenes
inferred← citeshttps://doi.org/10.1021/ol500403xopenalex-snapshot
Practical Synthesis of Phthalimides and Benzamides by a Multicomponent Reaction Involving Arynes, Isocyanides, and CO2/H2O
inferred← citeshttps://doi.org/10.1021/ol500959eopenalex-snapshot
Continuous-Flow Synthesis of Trimethylsilylphenyl Perfluorosulfonate Benzyne Precursors
inferred← citeshttps://doi.org/10.1039/9781837672615openalex-snapshot
Methods and Strategies for C–N Bond Formation Reactions
inferred← citeshttps://doi.org/10.1039/bk9781837672615-00222openalex-snapshot
Synthetic Methods for Diarylamines and Triarylamines
inferred← citeshttps://doi.org/10.1039/c5cc01757bopenalex-snapshot
Exploiting amphiphilicity: facile metal free access to thianthrenes and related sulphur heterocycles
inferred← citeshttps://doi.org/10.1039/c5ob01070eopenalex-snapshot
Metal and base free synthesis of primary amines via ipso amination of organoboronic acids mediated by [bis(trifluoroacetoxy)iodo]benzene (PIFA)
inferred← citeshttps://doi.org/10.1039/c5ob02418hopenalex-snapshot
Iron-catalyzed arylation of α-aryl-α-diazoesters
inferred← citeshttps://doi.org/10.1039/c6cc02235aopenalex-snapshot
Oxidative nucleophilic aromatic amination of nitrobenzenes
inferred← citeshttps://doi.org/10.1039/c7cc08553bopenalex-snapshot
Diverse ring opening of thietanes and other cyclic sulfides: an electrophilic aryne activation approach
inferred← citeshttps://doi.org/10.1039/c7cc09122bopenalex-snapshot
Recent advances in molecular rearrangements involving aryne intermediates
inferred← citeshttps://doi.org/10.1039/c7ob00914copenalex-snapshot
Aryne triggered [2,3]-sigmatropic rearrangement of allyl and propargyl thioethers
inferred← citeshttps://doi.org/10.1039/c7ob01596hopenalex-snapshot
Mild synthesis of triarylsulfonium salts with arynes
inferred← citeshttps://doi.org/10.1039/c8cc02176gopenalex-snapshot
Nucleophilic addition of tertiary propargylic amines to arynes followed by a [2,3]-sigmatropic rearrangement
inferred← citeshttps://doi.org/10.1039/c8cc03806fopenalex-snapshot
Tandem nucleophilic addition–cycloaddition of arynes with α-iminoesters: two concurrent pathways to imidazolidines
inferred← citeshttps://doi.org/10.1039/c8dt02346hopenalex-snapshot
Current advances in the catalytic conversion of carbon dioxide by molecular catalysts: an update
inferred← citeshttps://doi.org/10.1039/c8ob02507jopenalex-snapshot
A cascade process for the synthesis of ortho -formyl allyl aryl ethers and 2 H -chromen-2-ol derivatives from arynes via trapping of o -quinone methide with an activated alkene
inferred← citeshttps://doi.org/10.1039/c9cc05505copenalex-snapshot
1,2-Aminohalogenation of arynes with amines and organohalides
inferred← citeshttps://doi.org/10.1039/c9ob01157aopenalex-snapshot
Aryne insertion into the PO bond: one-pot synthesis of quaternary phosphonium triflates
inferred← citeshttps://doi.org/10.1039/d1nj04295eopenalex-snapshot
One-pot synthesis of 3-substituted-3-hydroxyindolin-2-ones: three component coupling of N -protected isatin, aryne precursor and 1,3-cyclodione under metal-free conditions
inferred← citeshttps://doi.org/10.1039/d1ob01690copenalex-snapshot
Iridium-catalyzed highly stereoselective deoxygenation of tertiary cycloalkanols: stereoelectronic insights and synthetic applications
inferred← citeshttps://doi.org/10.1039/d1qo01666kopenalex-snapshot
Transition-metal-free synthesis of 4-amino isoquinolin-1(2 H )-ones via a tandem reaction of arynes and oxazoles
inferred← citeshttps://doi.org/10.1039/d2cc04657aopenalex-snapshot
Substrate-controlled product divergence in the reaction of α-fluoro-β-ketoamides with arynes
inferred← citeshttps://doi.org/10.1039/d2cs00024eopenalex-snapshot
Functionalization of o -carboranes via carboryne intermediates
inferred← citeshttps://doi.org/10.1039/d2ob00447jopenalex-snapshot
Borane-catalyzed arylation of aryldiazoacetates with N , N -dialkylanilines
inferred← citeshttps://doi.org/10.1039/d5mr00109aopenalex-snapshot
Benzyne formations and reactions with amines under solvent-free conditions in a mixer mill
inferred← citeshttps://doi.org/10.1039/d6nj02660eopenalex-snapshot
Recyclable mesoporous SBA-15-anchored SPhos-palladium catalyst for the amination reaction of aryl chlorides
inferred← citeshttps://doi.org/10.1055/s-0036-1588868openalex-snapshot
Strategies for the Synthesis of N-Arylammonium Salts
inferred← citeshttps://doi.org/10.1055/s-0039-1690788openalex-snapshot
Facile Synthesis of π-Conjugated Heteroaromatic Compounds via Weak-Base-Promoted Transition-Metal-Free C–N Coupling
inferred← citeshttps://doi.org/10.1070/rcr4781openalex-snapshot
Arynes, diaryliodonium salts and azine N-oxides in transition metal-free electrophilic N-arylation
inferred← citeshttps://doi.org/10.1093/bulcsj/uoaf001openalex-snapshot
Synthesis of multisubstituted naphthalenes through consecutive aryne reactions
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.77.145openalex-snapshot
Synthetic Aryne Chemistry toward Multicomponent Coupling
inferred← citeshttps://doi.org/10.70675/b00b21ddz8fc2z408ez85a8zd04b8331c689openalex-snapshot
Hétéro-fonctionnalisation des composés aromatiques et hétéroaromatiques
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