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Palladium-Catalyzed C–C Bond Formation of Arylhydrazines with Olefins via Carbon–Nitrogen Bond Cleavage

https://doi.org/10.1021/ol202862t

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What this work says

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

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Palladium Oxidase Catalysis: Selective Oxidation of Organic Chemicals by Direct Dioxygen‐Coupled Turnover

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Catalytic Activation of NN Multiple Bonds: A Homogeneous Palladium Catalyst for Mechanistically Unprecedented Reduction of Azo Compounds

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Palladium/Copper‐Catalyzed Decarboxylative Cross‐Coupling of Aryl Chlorides with Potassium Carboxylates

inferredcites →https://doi.org/10.1002/anie.200805122openalex-snapshot

The Copper‐Catalyzed Decarboxylative Coupling of the sp3‐Hybridized Carbon Atoms of α‐Amino Acids

inferredcites →https://doi.org/10.1002/anie.200806273openalex-snapshot

Palladium(II)‐Catalyzed CH Activation/CC Cross‐Coupling Reactions: Versatility and Practicality

inferredcites →https://doi.org/10.1002/anie.200901884openalex-snapshot

Palladium‐Catalyzed Direct Arylation of Cyclic Enamides with Aryl Silanes by sp2 CH Activation

inferredcites →https://doi.org/10.1002/ejoc.201001620openalex-snapshot

Evolution and Synthetic Applications of the Heck–Matsuda Reaction: The Return of Arenediazonium Salts to Prominence

inferredcites →https://doi.org/10.1016/j.tet.2011.02.051openalex-snapshot

Recent advances in the Heck–Matsuda reaction in heterocyclic chemistry

inferredcites →https://doi.org/10.1021/ar960318popenalex-snapshot

Catalytic C−H/Olefin Coupling

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Ru-, Rh-, and Pd-Catalyzed C−C Bond Formation Involving C−H Activation and Addition on Unsaturated Substrates: Reactions and Mechanistic Aspects

inferredcites →https://doi.org/10.1021/cr0509861openalex-snapshot

Diazonium Salts as Substrates in Palladium-Catalyzed Cross-Coupling Reactions

inferredcites →https://doi.org/10.1021/cr068006fopenalex-snapshot

C−C, C−O, C−N Bond Formation on sp2 Carbon by Pd(II)-Catalyzed Reactions Involving Oxidant Agents

inferredcites →https://doi.org/10.1021/cr100209dopenalex-snapshot

Intermolecular Dehydrogenative Heck Reactions

inferredcites →https://doi.org/10.1021/cr900184eopenalex-snapshot

Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions

inferredcites →https://doi.org/10.1021/ja015683copenalex-snapshot

Oxygenation of Nitrogen-Coordinated Palladium(0): Synthetic, Structural, and Mechanistic Studies and Implications for Aerobic Oxidation Catalysis

inferredcites →https://doi.org/10.1021/ja027523mopenalex-snapshot

Development of a Decarboxylative Palladation Reaction and Its Use in a Heck-type Olefination of Arene Carboxylates

inferredcites →https://doi.org/10.1021/ja034908bopenalex-snapshot

The First Suzuki Cross-Couplings of Aryltrimethylammonium Salts

inferredcites →https://doi.org/10.1021/ja052099lopenalex-snapshot

On the Mechanism of the Palladium(II)-Catalyzed Decarboxylative Olefination of Arene Carboxylic Acids. Crystallographic Characterization of Non-Phosphine Palladium(II) Intermediates and Observation of Their Stepwise Transformation in Heck-like Processes

inferredcites →https://doi.org/10.1021/ja068993+openalex-snapshot

Biaryl Synthesis via Pd-Catalyzed Decarboxylative Coupling of Aromatic Carboxylates with Aryl Halides

inferredcites →https://doi.org/10.1021/ja0713431openalex-snapshot

Ruthenium-Catalyzed Carbon−Carbon Bond Formation via the Cleavage of an Unreactive Aryl Carbon−Nitrogen Bond in Aniline Derivatives with Organoboronates

inferredcites →https://doi.org/10.1021/ja100716xopenalex-snapshot

Palladium-Catalyzed Oxime Assisted Intramolecular Dioxygenation of Alkenes with 1 atm of Air as the Sole Oxidant

inferredcites →https://doi.org/10.1021/ja108998dopenalex-snapshot

Palladium-Catalyzed Bisolefination of C−C Triple Bonds: A Facile Method for the Synthesis of Naphthalene Derivatives

inferredcites →https://doi.org/10.1021/ja8050926openalex-snapshot

Decarboxylative Biaryl Synthesis from Aromatic Carboxylates and Aryl Triflates

inferredcites →https://doi.org/10.1021/ja8084548openalex-snapshot

Direct Cross-Coupling Reaction of Simple Alkenes with Acrylates Catalyzed by Palladium Catalyst

inferredcites →https://doi.org/10.1021/ja902829popenalex-snapshot

Cleavage of C−N Bonds in Aniline Derivatives on a Ruthenium Center and Its Relevance to Catalytic C−C Bond Formation

inferredcites →https://doi.org/10.1021/ja960092lopenalex-snapshot

Arylamine C−N Bond Oxidative Addition to (silox)3Ta (silox = tBu3SiO)

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/ol036436bopenalex-snapshot

Boron Trifluoride Induced Palladium-Catalyzed Cross-Coupling Reaction of 1-Aryltriazenes with Areneboronic Acids

inferredcites →https://doi.org/10.1021/ol048490dopenalex-snapshot

Azoles as Suzuki Cross-Coupling Leaving Groups: Syntheses of 6-Arylpurine 2‘-Deoxynucleosides and Nucleosides from 6-(Imidazol-1-yl)- and 6-(1,2,4-Triazol-4-yl)purine Derivatives1

inferredcites →https://doi.org/10.1039/c39880000975openalex-snapshot

Nickel-induced conversion of carbon–nitrogen into carbon–carbon bonds. One-step transformations of aryl, quaternary ammonium salts into alkylarenes and biaryls

inferredcites →https://doi.org/10.1126/science.1128684openalex-snapshot

Synthesis of Biaryls via Catalytic Decarboxylative Coupling

What points at this work

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

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inferred← citeshttps://doi.org/10.1002/9780471264194.fos07552.pub6openalex-snapshot

Palladium( II ) acetate

inferred← citeshttps://doi.org/10.1002/9780471264194.fos07552.pub7openalex-snapshot

Palladium( II ) acetate

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Homogeneous Transition‐Metal Catalyzed C–N Activation

inferred← citeshttps://doi.org/10.1002/9781118788981.ch5openalex-snapshot

Homogeneous Transition‐Metal‐Catalyzed C–O Bond Activation

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Palladium‐Catalyzed Direct Denitrogenative C‐3‐Arylation of 1H‐Indoles with Arylhydrazines using Air as the Oxidant

inferred← citeshttps://doi.org/10.1002/adsc.201300865openalex-snapshot

Transition Metal‐Mediated Direct CH Arylation of Heteroarenes Involving Aryl Radicals

inferred← citeshttps://doi.org/10.1002/adsc.201400155openalex-snapshot

Palladium‐Catalyzed CP Cross‐Coupling of Arylhydrazines with H‐Phosphonates via CN Bond Cleavage

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Copper‐Catalyzed Oxidative Carbamoylation of N‐Arylacrylamides with Hydrazinecarboxamides Leading to 2‐(Oxindol‐3‐yl)acetamides

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Aerobic Oxidative Functionalization of Indoles

inferred← citeshttps://doi.org/10.1002/ajoc.201300172openalex-snapshot

Palladium‐Catalyzed CH and CN Arylation of Aminothiazoles with Arylboronic Acids

inferred← citeshttps://doi.org/10.1002/ajoc.202200618openalex-snapshot

Synthesis of 2‐(Oxindol‐3‐yl)acetamides via Visible‐light‐mediated Oxidative Carbamoylation of N‐arylacrylamides

inferred← citeshttps://doi.org/10.1002/ajoc.202300413openalex-snapshot

Pd‐catalyzed Three‐component Cross‐coupling of Arylhydrazides with Arylboronic Acids and TFBen: Facile Access to Diaryl Ketones via Denitrogenative Carbonylation

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Catalyst‐Controlled Highly Selective Coupling and Oxygenation of Olefins: A Direct Approach to Alcohols, Ketones, and Diketones

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Transfer of Aryl Halide to Alkyl Halide: Reductive Elimination of Alkylhalide from Alkylpalladium Halides Containing syn‐β‐Hydrogen Atoms

inferred← citeshttps://doi.org/10.1002/ange.202310380openalex-snapshot

Orthogonal Olefination with Organogermanes

inferred← citeshttps://doi.org/10.1002/anie.201303917openalex-snapshot

Catalyst‐Controlled Highly Selective Coupling and Oxygenation of Olefins: A Direct Approach to Alcohols, Ketones, and Diketones

inferred← citeshttps://doi.org/10.1002/anie.201408341openalex-snapshot

Transfer of Aryl Halide to Alkyl Halide: Reductive Elimination of Alkylhalide from Alkylpalladium Halides Containing syn ‐β‐Hydrogen Atoms

inferred← citeshttps://doi.org/10.1002/anie.202310380openalex-snapshot

Orthogonal Olefination with Organogermanes

inferred← citeshttps://doi.org/10.1002/aoc.3108openalex-snapshot

Pd‐catalyzed homocoupling of arylhydrazines via C―N cleavage under O2

inferred← citeshttps://doi.org/10.1002/aoc.3227openalex-snapshot

Suzuki–Miyaura reactions promoted by a PdCl 2 /sulfonate‐tagged phenanthroline precatalyst in water

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.201700313openalex-snapshot

Mechanism of Nickel‐Catalyzed Suzuki–Miyaura Coupling of Amides

inferred← citeshttps://doi.org/10.1002/asia.202400126openalex-snapshot

Controllable Chemoselectivity Cascade Reactions for the Synthesis of Phenanthrenols via Palladium‐Catalyzed‐Suzuki/Heck Reaction and Michael Addition

inferred← citeshttps://doi.org/10.1002/chem.201103671openalex-snapshot

Oxidative Mizoroki–Heck‐Type Reaction of Arylsulfonyl Hydrazides for a Highly Regio‐ and Stereoselective Synthesis of Polysubstituted Alkenes

inferred← citeshttps://doi.org/10.1002/chem.201203832openalex-snapshot

Radical‐Mediated Diamination of Alkenes with Phenylhydrazine and Azodicarboxylates: Highly Diastereoselective Synthesis of trans‐Diamines from Cycloalkenes

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Aerobic Oxidative Coupling between Carbon Nucleophiles and Allylic Alcohols: A Strategy to Construct β‐(Hetero)Aryl Ketones and Aldehydes through Hydrogen Migration

inferred← citeshttps://doi.org/10.1002/chem.201304215openalex-snapshot

Palladium‐Catalyzed One‐Pot Three‐ or Four‐Component Coupling of Aryl Iodides, Alkynes, and Amines through CN Bond Cleavage: Efficient Synthesis of Indole Derivatives

inferred← citeshttps://doi.org/10.1002/chem.201604061openalex-snapshot

Unlocking Mizoroki–Heck‐Type Reactions of Aryl Cyanides Using Transfer Hydrocyanation as a Turnover‐Enabling Step

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.201214077openalex-snapshot

ChemInform Abstract: Palladium‐Catalyzed C—C Bond Formation of Arylhydrazines with Olefins via Carbon—Nitrogen Bond Cleavage.

inferred← citeshttps://doi.org/10.1002/ejoc.201400126openalex-snapshot

Palladium‐Catalyzed Suzuki Cross‐Coupling of Phenylhydrazine or (Phenylsulfonyl)hydrazine

inferred← citeshttps://doi.org/10.1002/ejoc.201800374openalex-snapshot

Palladium‐Catalyzed Regioselective C‐2 Arylation of Benzofurans with N′‐Acyl Arylhydrazines

inferred← citeshttps://doi.org/10.1002/slct.201902137openalex-snapshot

Synthesis, Characterization and Theoretical Investigation on Thiazoline‐Derived Palladium‐Complexes‐Catalyzed Denitrogenative Cross‐Coupling of Aryl Halides with Arylhydrazines

inferred← citeshttps://doi.org/10.1002/tcr.202100089openalex-snapshot

Recent Advances in the Pd‐Catalyzed Coupling of Arylhydrazines and Ammonium Salts via C−N Bond Cleavage

inferred← citeshttps://doi.org/10.1007/s11243-020-00443-3openalex-snapshot

Palladium-catalyzed denitrogenative cross-coupling of aryl halides with arylhydrazines under mild reaction conditions

inferred← citeshttps://doi.org/10.1016/j.catcom.2024.106862openalex-snapshot

Magnetically retractable tea extract stabilized palladium nanoparticles for denitrogenative cross-coupling of aryl bromides with arylhydrazines under green conditions: An alternate route for the biaryls synthesis

inferred← citeshttps://doi.org/10.1016/j.cogsc.2017.07.005openalex-snapshot

Recent advancements in palladium-catalyzed reactions involving molecular oxygen

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2013.06.001openalex-snapshot

Ruthenium-catalyzed reductive deamination and tandem alkylation of aniline derivatives

inferred← citeshttps://doi.org/10.1016/j.tet.2013.01.049openalex-snapshot

Heck–Matsuda reaction of arenediazonium salts in water

inferred← citeshttps://doi.org/10.1016/j.tet.2013.01.071openalex-snapshot

Palladium-catalyzed alkenyl C–H bond sulfonylation reaction using organosulfonyl chlorides

inferred← citeshttps://doi.org/10.1016/j.tet.2015.12.040openalex-snapshot

Iron-catalyzed C–C bond formation via cross dehydrative coupling reaction of N-heterocyclic aminols with electron rich arenes: facile access to C4-aryl-dihydroquinazolines

inferred← citeshttps://doi.org/10.1016/j.tet.2019.05.039openalex-snapshot

Copper-catalyzed denitrogenative N-arylation of sulfoximines and sulfonamides with arylhydrazines

inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.03.092openalex-snapshot

Palladium-catalyzed Suzuki cross-coupling of arylhydrazines via CNHNH2 bond activation in water

inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.06.095openalex-snapshot

Palladium-catalyzed denitrogenative Hiyama cross-coupling with arylhydrazines under air

inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.03.003openalex-snapshot

Iron-catalyzed C sp3 C sp3 bond formation via dehydrative cross coupling reaction: Facile access to new hybrid dihydroquinazolines having quinoline, isoquinoline, quinoxaline and azoles

inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.06.045openalex-snapshot

Pd/Cu-catalyzed facile approach to stilbenes: A novel diversity of TosMIC as an aryl source

inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00386openalex-snapshot

Transition-Metal-Catalyzed Cleavage of C–N Single Bonds

inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00380openalex-snapshot

Total Synthesis of Aryl C -Glycoside Natural Products: Strategies and Tactics

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.4c00915openalex-snapshot

Selective N -functionalization of Arylhydrazines with Primary Alcohols and Acids under PPh 3 /DDQ System

inferred← citeshttps://doi.org/10.1021/acs.joc.5b01633openalex-snapshot

Lewis Acid Mediated Tandem Reaction of Propargylic Alcohols with Hydroxylamine Hydrochloride To Give α,β-Unsaturated Amides and Alkenyl Nitriles

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.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.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.3c01684openalex-snapshot

N1-Allylation of Arylhydrazines via a Palladium-Catalyzed Allylic Substitution

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00449openalex-snapshot

Hydrogen Peroxide Promoted Mizoroki–Heck Reactions of Phenyldiazenes with Acrylates, Acrylamides, and Styrenes

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01412openalex-snapshot

I2/TBHP Mediated C–N and C–H Bond Cleavage of Tertiary Amines toward Selective Synthesis of Sulfonamides and β-Arylsulfonyl Enamines: The Solvent Effect on Reaction

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.8b00545openalex-snapshot

Direct Borylation of Tertiary Anilines via C–N Bond Activation

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.0c03341openalex-snapshot

Recent Methodologies That Exploit Oxidative Addition of C–N Bonds to Transition Metals

inferred← citeshttps://doi.org/10.1021/ja308950dopenalex-snapshot

Cyclopentadiene–Phosphine/Palladium-Catalyzed Cleavage of C–N Bonds in Secondary Amines: Synthesis of Pyrrole and Indole Derivatives from Secondary Amines and Alkenyl or Aryl Dibromides

inferred← citeshttps://doi.org/10.1021/ja310848xopenalex-snapshot

Palladium-Catalyzed Vinylation of Aminals with Simple Alkenes: A New Strategy To Construct Allylamines

inferred← citeshttps://doi.org/10.1021/ja501649aopenalex-snapshot

Nickel-Catalyzed Reductive and Borylative Cleavage of Aromatic Carbon–Nitrogen Bonds in N-Aryl Amides and Carbamates

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/10.1021/jm5014264openalex-snapshot

Synthesis and Bioactivity of β-Substituted Fosmidomycin Analogues Targeting 1-Deoxy- d -xylulose-5-phosphate Reductoisomerase

inferred← citeshttps://doi.org/10.1021/jo400261vopenalex-snapshot

Copper-Catalyzed Formal C–N Bond Cleavage of Aromatic Methylamines: Assembly of Pyridine Derivatives

inferred← citeshttps://doi.org/10.1021/jo401032ropenalex-snapshot

Oxidative Heck Reaction of Glycals and Aryl Hydrazines: A Palladium-Catalyzed C -Glycosylation

inferred← citeshttps://doi.org/10.1021/jo500026gopenalex-snapshot

Palladium-Catalyzed Suzuki Cross-Coupling of Arylhydrazines via C–N Bond Cleavage

inferred← citeshttps://doi.org/10.1021/jo501840uopenalex-snapshot

Controlling Olefin Isomerization in the Heck Reaction with Neopentyl Phosphine Ligands

inferred← citeshttps://doi.org/10.1021/jo502002wopenalex-snapshot

Oxidative Cleavage of Olefins by In Situ-Generated Catalytic 3,4,5,6-Tetramethyl-2-iodoxybenzoic Acid/Oxone

inferred← citeshttps://doi.org/10.1021/ol402921wopenalex-snapshot

Palladium(II)-Catalyzed ortho-Olefination of Arenes Applying Sulfoxides as Remote Directing Groups

inferred← citeshttps://doi.org/10.1021/ol501180qopenalex-snapshot

Beyond Directed Ortho Metalation: Ruthenium-Catalyzed Amide-Directed CAr–N Activation/C–C Coupling Reaction of Anthranilamides with Organoboronates

inferred← citeshttps://doi.org/10.1021/ol501766mopenalex-snapshot

Transition-Metal-Free Tandem Oxidative Removal of Benzylic Methylene Group by C–C and C–N Bond Cleavage Followed by Intramolecular New Aryl C–N Bond Formation under Radical Conditions

inferred← citeshttps://doi.org/10.1021/om3011855openalex-snapshot

Substituent Effects on Stoichiometric and Catalytic Cleavage of Carbon–Nitrogen Bonds in Aniline Derivatives by Ruthenium–Phosphine Complexes

inferred← citeshttps://doi.org/10.1038/ncomms12937openalex-snapshot

Stille coupling via C–N bond cleavage

inferred← citeshttps://doi.org/10.1039/c2ob26270copenalex-snapshot

Palladium-catalyzed desulfitative arylation of azoles with arylsulfonyl hydrazides

inferred← citeshttps://doi.org/10.1039/c3ob42444hopenalex-snapshot

Direct transformation of arylpropynes to acrylamides via a three-step tandem reaction

inferred← citeshttps://doi.org/10.1039/c4cc02876gopenalex-snapshot

Palladium-catalyzed thiolation of alkanes and ethers with arylsulfonyl hydrazides

inferred← citeshttps://doi.org/10.1039/c4cc05338aopenalex-snapshot

Preparation of highly substituted (β-acylamino)acrylates via iron-catalyzed alkoxycarbonylation of N-vinylacetamides with carbazates

inferred← citeshttps://doi.org/10.1039/c4gc02512aopenalex-snapshot

Cleavage of C–N bonds in carbon fiber/epoxy resin composites

inferred← citeshttps://doi.org/10.1039/c4ob02343aopenalex-snapshot

Copper( ii )-catalyzed coupling reaction: an efficient and regioselective approach to N′,N′-diaryl acylhydrazines

inferred← citeshttps://doi.org/10.1039/c4ra03421jopenalex-snapshot

Palladium-catalyzed Suzuki cross-couplings of N′-mesyl arylhydrazines via C–N bond cleavage

inferred← citeshttps://doi.org/10.1039/c4ra04621hopenalex-snapshot

Palladium and copper-catalyzed ligand-free coupling of phenylhydrazines in water

inferred← citeshttps://doi.org/10.1039/c5cc04111bopenalex-snapshot

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

inferred← citeshttps://doi.org/10.1039/c5cs00534eopenalex-snapshot

Transition-metal catalysed C–N bond activation

inferred← citeshttps://doi.org/10.1039/c5ob00133aopenalex-snapshot

Manganese catalysed sulfenylation of N-methyl amides with arenesulfonyl hydrazides

inferred← citeshttps://doi.org/10.1039/c5ob00432bopenalex-snapshot

Palladium( ii )-catalyzed direct alkenylation of dihydropyranones

inferred← citeshttps://doi.org/10.1039/c5ra05131bopenalex-snapshot

Palladium-catalyzed Heck coupling of arylhydrazines via C–NHNH 2 bond activation

inferred← citeshttps://doi.org/10.1039/c6cc04531fopenalex-snapshot

Nickel-catalyzed C–N bond reduction of aromatic and benzylic quaternary ammonium triflates

inferred← citeshttps://doi.org/10.1039/c6nj03718fopenalex-snapshot

Palladium/copper-catalyzed arylation of alkenes with N′-acyl arylhydrazines

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/c6ra03188aopenalex-snapshot

Open-air oxidative Mizoroki–Heck reaction of arylsulfonyl hydrazides with alkenes

inferred← citeshttps://doi.org/10.1039/c7gc02775copenalex-snapshot

Highly selective sp 3 C–N bond activation of tertiary anilines modulated by steric and thermodynamic factors

inferred← citeshttps://doi.org/10.1039/c7ra02549aopenalex-snapshot

Palladium catalyzed Suzuki cross-coupling of benzyltrimethylammonium salts via C–N bond cleavage

inferred← citeshttps://doi.org/10.1039/c7ra09947aopenalex-snapshot

Poly(o-aminothiophenol)-stabilized Pd nanoparticles as efficient heterogenous catalysts for Suzuki cross-coupling reactions

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/d0qi01052aopenalex-snapshot

Synthesis of a palladium based MOF via an effective post-synthetic modification approach and its catalytic activity towards Heck type coupling reactions

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/10.1039/d6qo00990eopenalex-snapshot

Switchable regioselective and stereoselective synthesis of but-3-enoates and ( E )-but-2-enoates with calcium carbide as an inorganic C2 source

inferred← citeshttps://doi.org/10.1080/00397911.2020.1725577openalex-snapshot

Ligand-free copper-catalyzed denitrogenative arylation of phosphorylamides with arylhydrazines

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/10.11606/d.46.2021.tde-09112021-093303openalex-snapshot

Acoplamento cruzado de aril-hidrazinas e arenotióis catalisado por paládio: uma investigação computacional

inferred← citeshttps://doi.org/10.1371/journal.pone.0176189openalex-snapshot

Bioactivity and structure-activity relationship of cinnamic acid esters and their derivatives as potential antifungal agents for plant protection

inferred← citeshttps://doi.org/10.1515/chem-2018-0058openalex-snapshot

Metal-mediated reactions towards the synthesis of a novel deaminolysed bisurea, dicarbamolyamine

inferred← citeshttps://doi.org/10.3390/catal14060338openalex-snapshot

Na2SO3-Promoted Heck Coupling and Homo-Coupling of Arylhydrazines at Room Temperature

inferred← citeshttps://doi.org/10.3390/reactions5010006openalex-snapshot

Oxidative Cleavage of 9,10-Dihydroxystearic Acid on Supported Au, Pd and PdAu Nanoparticle-Based Catalysts

inferred← citeshttps://doi.org/10.70675/716dc364z97eez4055zb765z0d6b3e226d07openalex-snapshot

Vers la première synthèse totale de la kidamycine : développement d’une stratégie de synthèse convergente et innovante, et mise au point d’une réaction d’aryl-C-glycosylation stéréospécifique

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