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Palladium-catalyzed aerobic oxidative cross-coupling of arylhydrazines with terminal alkynes

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

inferredcites →https://doi.org/10.1002/1521-3773(20000804)39:15<2632::aid-anie2632>3.0.co;2-fopenalex-snapshot
Acetylenic Coupling: A Powerful Tool in Molecular Construction
inferredcites →https://doi.org/10.1002/adsc.201200997openalex-snapshot
Palladium‐Catalyzed Direct Denitrogenative C‐3‐Arylation of 1H‐Indoles with Arylhydrazines using Air as the Oxidant
inferredcites →https://doi.org/10.1002/adsc.201400155openalex-snapshot
Palladium‐Catalyzed CP Cross‐Coupling of Arylhydrazines with H‐Phosphonates via CN Bond Cleavage
inferredcites →https://doi.org/10.1002/anie.200502071openalex-snapshot
Synthesis of Naturally Occurring Polyynes
inferredcites →https://doi.org/10.1002/anie.200503875openalex-snapshot
Catalytic Activation of NN Multiple Bonds: A Homogeneous Palladium Catalyst for Mechanistically Unprecedented Reduction of Azo Compounds
inferredcites →https://doi.org/10.1002/anie.200602761openalex-snapshot
Palladium‐Based Catalytic Systems for the Synthesis of Conjugated Enynes by Sonogashira Reactions and Related Alkynylations
inferredcites →https://doi.org/10.1002/anie.201303917openalex-snapshot
Catalyst‐Controlled Highly Selective Coupling and Oxygenation of Olefins: A Direct Approach to Alcohols, Ketones, and Diketones
inferredcites →https://doi.org/10.1002/aoc.3108openalex-snapshot
Pd‐catalyzed homocoupling of arylhydrazines via C―N cleavage under O2
inferredcites →https://doi.org/10.1002/chem.201003060openalex-snapshot
A Mild Oxidative Aryl Radical Addition into Alkenes by Aerobic Oxidation of Arylhydrazines
inferredcites →https://doi.org/10.1002/ejoc.200500095openalex-snapshot
Enantioselective Synthesis of (+)‐(S)‐Laudanosine and (–)‐(S)‐Xylopinine
inferredcites →https://doi.org/10.1002/ejoc.201300917openalex-snapshot
o‐Iodoxybenzoic Acid Mediated N‐Arylation of Aromatic Amines by Using Arylhydrazines as the Arylating Counterpart
inferredcites →https://doi.org/10.1016/j.jorganchem.2004.05.032openalex-snapshot
Mechanism of the carbopalladation of alkynes by aryl-palladium complexes
inferredcites →https://doi.org/10.1016/j.tetlet.2005.10.001openalex-snapshot
Synthetic approach to enyne and enediyne analogues of anticancer agents
inferredcites →https://doi.org/10.1016/j.tetlet.2009.08.113openalex-snapshot
Copper- and base-free Sonogashira-type cross-coupling reaction of triarylantimony dicarboxylates with terminal alkynes under an aerobic condition
inferredcites →https://doi.org/10.1016/j.tetlet.2010.11.099openalex-snapshot
A base-free, one-pot diazotization/cross-coupling of anilines with arylboronic acids
inferredcites →https://doi.org/10.1016/j.tetlet.2014.03.092openalex-snapshot
Palladium-catalyzed Suzuki cross-coupling of arylhydrazines via CNHNH2 bond activation in water
inferredcites →https://doi.org/10.1016/j.tetlet.2014.06.099openalex-snapshot
Air-promoted direct radical arylation of anilines with arylhydrazines
inferredcites →https://doi.org/10.1016/s0022-328x(00)94048-8openalex-snapshot
Synthesis of aryl- and vinyl-substituted acetylene derivatives by the use of nickel and palladium complexes
inferredcites →https://doi.org/10.1016/s0022-328x(00)94049-xopenalex-snapshot
Palladium catalyzed synthesis of aryl, heterocyclic and vinylic acetylene derivatives
inferredcites →https://doi.org/10.1016/s0040-4020(02)01001-3openalex-snapshot
Manganese(III) acetate-mediated oxidative coupling of phenylhydrazines with furan and thiophene: a novel method for hetero biaryl coupling
inferredcites →https://doi.org/10.1016/s0040-4039(00)91094-3openalex-snapshot
A convenient synthesis of acetylenes: catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines
inferredcites →https://doi.org/10.1016/s0040-4039(01)80781-4openalex-snapshot
Aryl radicals by copper(II) oxidation of hydrazines: A new method for the oxidative and reductive arylation of alkenes
inferredcites →https://doi.org/10.1021/acs.joc.5b00739openalex-snapshot
Transition-Metal-Free C-3 Arylation of Quinoline-4-ones with Arylhydrazines
inferredcites →https://doi.org/10.1021/ar0000612openalex-snapshot
Molecular Electronics. Synthesis and Testing of Components
inferredcites →https://doi.org/10.1021/cr020377iopenalex-snapshot
Palladium-Catalyzed Alkynylation
inferredcites →https://doi.org/10.1021/cr050992xopenalex-snapshot
The Sonogashira Reaction: A Booming Methodology in Synthetic Organic Chemistry
inferredcites →https://doi.org/10.1021/cr9500287openalex-snapshot
Conjugated Macromolecules of Precise Length and Constitution. Organic Synthesis for the Construction of Nanoarchitectures
inferredcites →https://doi.org/10.1021/ja063710zopenalex-snapshot
Oxidative Palladium(II) Catalysis: A Highly Efficient and Chemoselective Cross-Coupling Method for Carbon−Carbon Bond Formation under Base-Free and Nitrogenous-Ligand Conditions
inferredcites →https://doi.org/10.1021/jo01047a008openalex-snapshot
The Substitution of Aryl Iodides with Cuprous Acetylides. A Synthesis of Tolanes and Heterocyclics 1
inferredcites →https://doi.org/10.1021/jo01300a018openalex-snapshot
Arylation and alkylation of olefins by arylamines or hydrazines via the carbon-nitrogen bond cleavage in the presence of palladium(II) salts
inferredcites →https://doi.org/10.1021/jo047894gopenalex-snapshot
One-Pot Sequential Synthesis of Acetoxylated [60]Fullerene Derivatives
inferredcites →https://doi.org/10.1021/jo049259gopenalex-snapshot
Highly Diastereoselective Approach toward (±)-Tetraponerine T6 and Analogues via the Double Cycloisomerization−Reduction of Bis-alkynylpyrimidines
inferredcites →https://doi.org/10.1021/jo301980jopenalex-snapshot
Regioselective Radical Arylation of Anilines with Arylhydrazines
inferredcites →https://doi.org/10.1021/jo4022474openalex-snapshot
Copper-Catalyzed Coupling Reaction of Arylhydrazines and Trialkylphosphites
inferredcites →https://doi.org/10.1021/jo500026gopenalex-snapshot
Palladium-Catalyzed Suzuki Cross-Coupling of Arylhydrazines via C–N Bond Cleavage
inferredcites →https://doi.org/10.1021/jo500063ropenalex-snapshot
Oxidative Radical Arylation of Anilines with Arylhydrazines and Dioxygen from Air
inferredcites →https://doi.org/10.1021/ol202862topenalex-snapshot
Palladium-Catalyzed C–C Bond Formation of Arylhydrazines with Olefins via Carbon–Nitrogen Bond Cleavage
inferredcites →https://doi.org/10.1021/ol900110gopenalex-snapshot
1,4-Fullerenols C 60 ArOH: Synthesis and Functionalization
inferredcites →https://doi.org/10.1039/b105119aopenalex-snapshot
Manganese(iii) acetate-mediated oxidative coupling of phenylhydrazines with benzene: a novel method for biaryl coupling
inferredcites →https://doi.org/10.1039/b509316copenalex-snapshot
Synthesis, processing and properties of conjugated polymer networks
inferredcites →https://doi.org/10.1039/c1cs15071eopenalex-snapshot
Recent advances in Sonogashira reactions
inferredcites →https://doi.org/10.1039/c2cc31737kopenalex-snapshot
Palladium-catalyzed monoselective C–H borylation of acetanilides under acidic conditions
inferredcites →https://doi.org/10.1039/c4ob00798kopenalex-snapshot
CoPc-catalyzed selective radical arylation of anilines with arylhydrazines for synthesis of 2-aminobiaryls
inferredcites →https://doi.org/10.1039/j39690001663openalex-snapshot
Oxidation of hydrazine derivatives. Part I. Oxidation of phenyl-hydrazine with lead tetra-acetate
inferredcites →https://doi.org/10.1246/bcsj.56.1113openalex-snapshot
The Reductive Coupling of Organic Halide Using Hydrazine and a Palladium Amalgam Catalyst. II. Homocoupling of Haloarene with Arylhydrazine
inferredcites →https://doi.org/10.1246/bcsj.61.2185openalex-snapshot
Barium Ferrate Monohydrate BaFeO4·H2O, a Useful Oxidant for the Oxidation of Organic Compounds under Aprotic Conditions

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.4685044openalex-extracted
Preparation of Heterogeneous Magnetic Nanocatalysts Based on Reduced Graphene Oxide with Nickel and Cobalt Particles and Investigation of its Activity in Heck and Sonogashira Cross-Coupling Reactions and 4-Nitrophenol Reduction
inferred← citeshttps://doi.org/10.1002/0471264180.or116.01openalex-snapshot
A Half Century of the Sonogashira Reaction
inferred← citeshttps://doi.org/10.1002/adsc.201901607openalex-snapshot
Electrochemical Sulfonylation of Alkynes with Sulfonyl Hydrazides: A Metal‐ and Oxidant‐Free Protocol for the Synthesis of Alkynyl Sulfones
inferred← citeshttps://doi.org/10.1002/aoc.4203openalex-snapshot
Denitrogenative Pd/Cu‐catalyzed Suzuki‐type Cross‐coupling of Aryltrifluoroborates with Arylhydrazine Hydrochlorides in Water under Room Temperature
inferred← citeshttps://doi.org/10.1002/asia.202000117openalex-snapshot
Nickel or Palladium‐Catalyzed Decarbonylative Transformations of Carboxylic Acid Derivatives
inferred← citeshttps://doi.org/10.1002/chem.202202449openalex-snapshot
Temperature‐Controlled Selective Mono‐ vs. Di‐ortho‐Arylation for the Synthesis of Arylhydrazine Derivatives
inferred← citeshttps://doi.org/10.1002/chin.201552064openalex-snapshot
ChemInform Abstract: Palladium‐Catalyzed Aerobic Oxidative Cross‐Coupling of Arylhydrazines with Terminal Alkynes.
inferred← citeshttps://doi.org/10.1002/cjoc.202300310openalex-snapshot
Palladium‐Catalyzed Denitrogenative Self‐carbonylation of Arylhydrazine Using CO and O2 as an Ideal Oxidant†
inferred← citeshttps://doi.org/10.1002/ejoc.202400635openalex-snapshot
Palladium‐Catalyzed Denitrogenative Coupling of Aryldiazonium Salts with Terminal Alkynes for the Assembly of Internal Alkynes
inferred← citeshttps://doi.org/10.1002/slct.202404669openalex-snapshot
Overview of Phenylhydrazine‐Based Organic Transformations
inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00027-8openalex-snapshot
Alkynes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2021.121749openalex-snapshot
Pd-NHCs Enabled Suzuki-Miyaura Cross-Coupling of Arylhydrazines via C–N Bond Cleavage
inferred← citeshttps://doi.org/10.1016/j.matpr.2022.11.083openalex-snapshot
Sonogashira reaction cum cyclization under microwave irradiation supported by sodium aluminate (NaAlO2) and catalyzed by zinc: A green alternative approach in production of furo[3,2-h]quinolones
inferred← citeshttps://doi.org/10.1016/j.saa.2021.119574openalex-snapshot
Vibrational spectroscopy and DFT analysis of 4-cyanophenylhydrazine: A potential SERS probe
inferred← citeshttps://doi.org/10.1016/j.snb.2017.10.119openalex-snapshot
Construction of a coumarin based fluorescent sensing platform for palladium and hydrazine detection
inferred← citeshttps://doi.org/10.1016/j.tet.2019.05.034openalex-snapshot
Iodine-mediated aryl transfer reaction from arylhydrazine hydrochlorides to nitriles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.151647openalex-snapshot
Palladium-catalyzed alkynylation of aromatic amines via in situ formed trimethylammonium salts
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01323openalex-snapshot
Approach to the Synthesis of Unsymmetrical/Symmetrical Maleimides via Desulfitative Arylation at Different Temperatures
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01115openalex-snapshot
Palladium-Catalyzed Oxidative Nonclassical Heck Reaction of Arylhydrazines with Allylic Alcohols via C–N Bond Cleavage: Access to β-Arylated Carbonyl Compounds
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02034openalex-snapshot
Palladium-Catalyzed Oxidative Heck-Type Reaction of Allylic Acetates with Arylhydrazines as Arylation Reagents via β-OAc Elimination
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01594openalex-snapshot
Fe-Catalyzed Aerobic Oxidative C–CN Bond Cleavage of Arylacetonitriles Leading to Various Esters
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02697openalex-snapshot
Palladium-Catalyzed Denitrogenative Synthesis of Aryl Ketones from Arylhydrazines and Nitriles Using O2 as Sole Oxidant
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00499openalex-snapshot
Palladium-Catalyzed Oxidative Carbonylation of Aryl Hydrazines with CO and O 2 at Atmospheric Pressure
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00899openalex-snapshot
Palladium-Catalyzed Desulfitative Cross-Coupling of Arylsulfonyl Hydrazides with Terminal Alkynes: A General Approach toward Functionalized Internal Alkynes
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01215openalex-snapshot
Hypervalent Iodine(III)-Promoted Phenyl Transfer Reaction from Phenyl Hydrazides to Nitriles
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02926openalex-snapshot
Palladium-Catalyzed Oxidative Cross-Coupling of Arylhydrazines and Arenethiols with Molecular Oxygen as the Sole Oxidant
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00451openalex-snapshot
Surfactant-Type Catalyst for Aerobic Oxidative Coupling of Hydrazine with Thiol in Water
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02364openalex-snapshot
Photoinduced Copper-Catalyzed Site-Selective C(sp2)–C(sp) Cross-Coupling via Aryl Sulfonium Salts
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01447openalex-snapshot
A Regioselective Approach to Trisubstituted Pyrazoles via Palladium-Catalyzed Oxidative Sonogashira-Carbonylation of Arylhydrazines
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02312openalex-snapshot
Highly Regioselective Carbamoylation of Electron-Deficient Nitrogen Heteroarenes with Hydrazinecarboxamides
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00949openalex-snapshot
Palladium-Catalyzed Decarbonylative Alkynylation of Amides
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03549openalex-snapshot
Visible-Light-Mediated Synthesis of Unsymmetrical Diaryl Sulfides via Oxidative Coupling of Arylhydrazine with Thiol
inferred← citeshttps://doi.org/10.1021/acscatal.9b00218openalex-snapshot
Sonogashira Cross-Coupling of Aryltrimethylammonium Salts
inferred← citeshttps://doi.org/10.1021/jacs.1c06036openalex-snapshot
Electrochemical Palladium-Catalyzed Oxidative Sonogashira Carbonylation of Arylhydrazines and Alkynes to Ynones
inferred← citeshttps://doi.org/10.1021/jacs.7b08579openalex-snapshot
Low-Valent, High-Spin Chromium-Catalyzed Cleavage of Aromatic Carbon–Nitrogen Bonds at Room Temperature: A Combined Experimental and Theoretical Study
inferred← citeshttps://doi.org/10.1039/c6qo00634eopenalex-snapshot
Acid-promoted denitrogenative Pd-catalyzed addition of arylhydrazines with nitriles at room temperature
inferred← citeshttps://doi.org/10.1039/c8gc01180jopenalex-snapshot
Visible-light induced copper( i )-catalysed denitrogenative oxidative coupling of hydrazinylpyridines with terminal alkynes
inferred← citeshttps://doi.org/10.1039/c8ob00305jopenalex-snapshot
Denitrogenative palladium-catalyzed coupling of aryl halides with arylhydrazines under mild conditions
inferred← citeshttps://doi.org/10.1039/c8ra06423gopenalex-snapshot
Arylhydrazines: novel and versatile electrophilic partners in cross-coupling reactions
inferred← citeshttps://doi.org/10.1039/c9cc08663copenalex-snapshot
Palladium-catalyzed denitrative Sonogashira-type cross-coupling of nitrobenzenes with terminal alkynes
inferred← citeshttps://doi.org/10.1039/d0cc03309jopenalex-snapshot
Palladium/copper-cocatalyzed decarbonylative alkynylation of acyl fluorides with alkynylsilanes: synthesis of unsymmetrical diarylethynes
inferred← citeshttps://doi.org/10.1039/d0ra01043jopenalex-snapshot
The synthesis of quinolines via denitrogenative palladium-catalyzed cascade reaction of o -aminocinnamonitriles with arylhydrazines
inferred← citeshttps://doi.org/10.1039/d6qo00986gopenalex-snapshot
Regioselective palladium-catalyzed asymmetric N 1 -allylic substitution of allyl acetates with arylhydrazines via kinetic resolution
inferred← citeshttps://doi.org/10.1055/s-0040-1705954openalex-snapshot
Nickel-Catalyzed Decarbonylative Alkynylation of Acyl Fluorides with Terminal Alkynes under Copper-Free Conditions
inferred← citeshttps://doi.org/10.1080/01614940.2019.1702191openalex-snapshot
Catalytic advances in direct functionalizations using arylated hydrazines as the building blocks
inferred← citeshttps://doi.org/10.1080/17568919.2024.2389772openalex-snapshot
New 6-nitro-4-substituted quinazoline derivatives targeting epidermal growth factor receptor: design, synthesis and in vitro anticancer studies
inferred← citeshttps://doi.org/10.24820/ark.5550190.p012.011openalex-snapshot
Catalytic alkynylations through the activation of C-N bonds
inferred← citeshttps://doi.org/10.3389/fmats.2019.00273openalex-snapshot
Hydrothermally Synthesized CuCo2S4 Nanosheets as an Easily Accessible and Convenient Heterogeneous Catalyst for the Sonogashira Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.70675/e80d1290z2934z43a7zaf74z651037cd5d09openalex-snapshot
Taming highly reactive metal cations and intermediates in homogeneous catalysis using a weakly coordinating anion
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