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Palladium-catalyzed carbonylation of benzylic ammonium salts to amides and esters via C–N bond activation

https://doi.org/10.1039/c8ob00488a
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What this work says

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

inferredcites →https://doi.org/10.1002/9781118662083openalex-snapshot
Comprehensive Organic Transformations
inferredcites →https://doi.org/10.1002/ange.201600697openalex-snapshot
Nickel‐Catalyzed Carboxylation of Benzylic C−N Bonds with CO2
inferredcites →https://doi.org/10.1002/anie.200900013openalex-snapshot
Palladium‐Catalyzed Carbonylation Reactions of Aryl Halides and Related Compounds
inferredcites →https://doi.org/10.1002/anie.201100683openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of Aryltrimethylammonium Iodides with Organozinc Reagents
inferredcites →https://doi.org/10.1002/anie.201100763openalex-snapshot
Oxidative Carbonylation Reactions: Organometallic Compounds (RM) or Hydrocarbons (RH) as Nucleophiles
inferredcites →https://doi.org/10.1002/anie.201605104openalex-snapshot
Selective Palladium‐Catalyzed Aminocarbonylation of Olefins to Branched Amides
inferredcites →https://doi.org/10.1002/anie.201702292openalex-snapshot
Carbonylations with CO2 as the CO Source and Reactivity Modifier
inferredcites →https://doi.org/10.1002/anie.201709807openalex-snapshot
Ligand‐ and Solvent‐Controlled Regio‐ and Chemodivergent Carbonylative Reactions
inferredcites →https://doi.org/10.1002/cctc.200900062openalex-snapshot
Palladium‐Catalyzed Carbonylation Reactions of Alkenes and Alkynes
inferredcites →https://doi.org/10.1002/cctc.201100268openalex-snapshot
Palladium‐Catalyzed Aminocarbonylation of Benzyl Chlorides using Ammonia
inferredcites →https://doi.org/10.1002/chem.201301774openalex-snapshot
A General Palladium‐Catalyzed Carbonylative Synthesis of Chromenones from Salicylic Aldehydes and Benzyl Chlorides
inferredcites →https://doi.org/10.1002/chem.201503596openalex-snapshot
Making Dimethylamino a Transformable Directing Group by Nickel‐Catalyzed CN Borylation
inferredcites →https://doi.org/10.1002/chem.201603436openalex-snapshot
Cross‐Coupling of Organolithium with Ethers or Aryl Ammonium Salts by C−O or C−N Bond Cleavage
inferredcites →https://doi.org/10.1007/3418_024openalex-snapshot
Oxidative Carbonylations
inferredcites →https://doi.org/10.1007/b114222openalex-snapshot
Advanced Organic Chemistry
inferredcites →https://doi.org/10.1016/j.molcata.2013.10.014openalex-snapshot
Carbonylation of quaternary ammonium salts to tertiary amides using NaCo(CO)4 catalyst
inferredcites →https://doi.org/10.1016/j.tet.2005.08.031openalex-snapshot
Amide bond formation and peptide coupling
inferredcites →https://doi.org/10.1016/j.tet.2010.03.090openalex-snapshot
Pd-catalysed carbonylations: versatile technology for discovery and process chemists
inferredcites →https://doi.org/10.1016/j.tet.2013.09.039openalex-snapshot
Iron-catalyzed cross-coupling of aryltrimethylammonium triflates and alkyl Grignard reagents
inferredcites →https://doi.org/10.1016/j.tetlet.2009.11.023openalex-snapshot
One-pot amide synthesis from allyl or benzyl halides and amines by Pd-catalysed carbonylation
inferredcites →https://doi.org/10.1021/acs.joc.5b02557openalex-snapshot
Nickel-Catalyzed Borylation of Aryl- and Benzyltrimethylammonium Salts via C–N Bond Cleavage
inferredcites →https://doi.org/10.1021/acs.joc.7b00009openalex-snapshot
Natural Product Synthesis via Palladium-Catalyzed Carbonylation
inferredcites →https://doi.org/10.1021/acs.joc.7b00499openalex-snapshot
Palladium-Catalyzed Oxidative Carbonylation of Aryl Hydrazines with CO and O 2 at Atmospheric Pressure
inferredcites →https://doi.org/10.1021/acs.orglett.5b02458openalex-snapshot
Palladium-Catalyzed C–H Arylation of (Benzo)oxazoles or (Benzo)thiazoles with Aryltrimethylammonium Triflates
inferredcites →https://doi.org/10.1021/acs.orglett.5b03455openalex-snapshot
Nickel-Catalyzed Borylation of Benzylic Ammonium Salts: Stereospecific Synthesis of Enantioenriched Benzylic Boronates
inferredcites →https://doi.org/10.1021/acs.orglett.7b01488openalex-snapshot
Charge-Transfer Complex Promoted C–N Bond Activation for Ni-Catalyzed Carbonylation
inferredcites →https://doi.org/10.1021/acscatal.6b01939openalex-snapshot
Palladium-Catalyzed Intramolecular Hydroaminocarbonylation to Lactams: Additive-Free Protocol Initiated by Palladium Hydride
inferredcites →https://doi.org/10.1021/acscatal.7b04116openalex-snapshot
Palladium-Catalyzed Carbonylative Direct Transformation of Benzyl Amines under Additive-Free Conditions
inferredcites →https://doi.org/10.1021/cr010328qopenalex-snapshot
Palladium-Catalyzed Reppe Carbonylation
inferredcites →https://doi.org/10.1021/cr300100sopenalex-snapshot
Synthesis of Heterocycles via Palladium-Catalyzed Carbonylations
inferredcites →https://doi.org/10.1021/cr9000836openalex-snapshot
Transition Metal-Catalyzed Direct Arylation of Substrates with Activated sp 3 -Hybridized C−H Bonds and Some of Their Synthetic Equivalents with Aryl Halides and Pseudohalides
inferredcites →https://doi.org/10.1021/cs200434sopenalex-snapshot
Carbonylation of Metal Carbene with Carbon Monoxide: Generation of Ketene
inferredcites →https://doi.org/10.1021/cs500922xopenalex-snapshot
Palladium-Catalyzed Carbonylative Transformation of C(sp 3 )–X Bonds
inferredcites →https://doi.org/10.1021/ja00832a024openalex-snapshot
Palladium-catalyzed formylation of aryl, heterocyclic, and vinylic halides
inferredcites →https://doi.org/10.1021/ja034908bopenalex-snapshot
The First Suzuki Cross-Couplings of Aryltrimethylammonium Salts
inferredcites →https://doi.org/10.1021/ja3036459openalex-snapshot
Palladium-Catalyzed Oxidative Carbonylation of Benzylic C–H Bonds via Nondirected C(sp3)–H Activation
inferredcites →https://doi.org/10.1021/ja3089422openalex-snapshot
Nickel-Catalyzed Cross Couplings of Benzylic Ammonium Salts and Boronic Acids: Stereospecific Formation of Diarylethanes via C–N Bond Activation
inferredcites →https://doi.org/10.1021/jacs.6b03161openalex-snapshot
Highly Ligand-Controlled Regioselective Pd-Catalyzed Aminocarbonylation of Styrenes with Aminophenols
inferredcites →https://doi.org/10.1021/jacs.6b08164openalex-snapshot
Ion Pair-Directed Regiocontrol in Transition-Metal Catalysis: A Meta-Selective C–H Borylation of Aromatic Quaternary Ammonium Salts
inferredcites →https://doi.org/10.1021/jacs.7b05273openalex-snapshot
Regio- and Stereospecific Copper-Catalyzed Substitution Reaction of Propargylic Ammonium Salts with Aryl Grignard Reagents
inferredcites →https://doi.org/10.1021/jo00937a003openalex-snapshot
Palladium-catalyzed carboalkoxylation of aryl, benzyl, and vinylic halides
inferredcites →https://doi.org/10.1021/jo00937a004openalex-snapshot
Palladium-catalyzed amidation of aryl, heterocyclic, and vinylic halides
inferredcites →https://doi.org/10.1021/ol063042mopenalex-snapshot
Benzylic Substitution of Gramines with Boronic Acids and Rhodium or Iridium Catalysts†
inferredcites →https://doi.org/10.1021/ol1018739openalex-snapshot
Room Temperature Palladium-Catalyzed Cross Coupling of Aryltrimethylammonium Triflates with Aryl Grignard Reagents
inferredcites →https://doi.org/10.1021/ol401419uopenalex-snapshot
Palladium-Catalyzed Oxidative Aminocarbonylation: A New Entry to Amides via C–H Activation
inferredcites →https://doi.org/10.1021/om800549qopenalex-snapshot
Palladium-Catalyzed Carbonylation—A Reaction Come of Age
inferredcites →https://doi.org/10.1038/ncomms12937openalex-snapshot
Stille coupling via C–N bond cleavage
inferredcites →https://doi.org/10.1039/b701677hopenalex-snapshot
Amide bond formation: beyond the myth of coupling reagents
inferredcites →https://doi.org/10.1039/c1cs15109fopenalex-snapshot
Palladium-catalyzed carbonylative coupling reactions between Ar–X and carbon nucleophiles
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/10.1039/c3cc47015fopenalex-snapshot
Amide bond formation via C(sp 3 )–H bond functionalization and CO insertion
inferredcites →https://doi.org/10.1039/c3ob41989dopenalex-snapshot
Nickel-catalyzed cross-coupling of aryltrimethylammonium triflates and amines
inferredcites →https://doi.org/10.1039/c4cc02167copenalex-snapshot
Acid-free regioselective aminocarbonylation of alkenes
inferredcites →https://doi.org/10.1039/c4qo00321gopenalex-snapshot
Highly efficient pincer nickel catalyzed cross-coupling of aryltrimethylammonium triflates with arylzinc reagents
inferredcites →https://doi.org/10.1039/c5cs00534eopenalex-snapshot
Transition-metal catalysed C–N bond activation
inferredcites →https://doi.org/10.1039/c7gc03619aopenalex-snapshot
A sustainable procedure toward alkyl arylacetates: palladium-catalysed direct carbonylation of benzyl alcohols in organic carbonates
inferredcites →https://doi.org/10.1039/c7ra02549aopenalex-snapshot
Palladium catalyzed Suzuki cross-coupling of benzyltrimethylammonium salts via C–N bond cleavage
inferredcites →https://doi.org/10.1039/c7sc04054gopenalex-snapshot
Palladium-catalyzed regiodivergent hydroaminocarbonylation of alkenes to primary amides with ammonium chloride
inferredcites →https://doi.org/10.1080/00397910600773759openalex-snapshot
Regiospecific Phenyl Esterification to Some Organic Acids Catalyzed by Combined Lewis Acids
inferredcites →https://doi.org/10.1080/00397919308013807openalex-snapshot
A Simple Preparation of Amides from Acids and Amines by Heating of Their Mixture
inferredcites →https://doi.org/10.1213/00000539-198308000-00015openalex-snapshot
Basic and Clinical Pharmacology
inferredcites →https://doi.org/10.2174/1385272023373699openalex-snapshot
Synthetic Applications of Palladium Catalysed Carbonylation of Organic Halides

What points at this work

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

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3‐Bromo‐ N,N,N ‐trimethylanilinium Iodide (1:1)
inferred← citeshttps://doi.org/10.1002/9783527831883.ch10openalex-snapshot
Carbonylation of C (sp3) X Bonds Utilizing CO
inferred← citeshttps://doi.org/10.1002/adsc.202001561openalex-snapshot
Palladium Catalyzed Aminocarbonylation of Benzylic Ammonium Triflates with Nitroarenes: Synthesis of Phenylacetamides
inferred← citeshttps://doi.org/10.1002/asia.70212openalex-snapshot
Photoredox‐catalyzed Divergent Defluorofunctionalizations of gem‐difluoroarylalkenes with Nucleophiles to Access α‐arylated Carboxylic Acids and its Derivatives
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Photoinduced C(sp3)−N Bond Cleavage Leading to the Stereoselective Syntheses of Alkenes
inferred← citeshttps://doi.org/10.1002/ejoc.201901592openalex-snapshot
Palladium‐Catalyzed Alkoxycarbonylation of sec‐Benzylic Ethers
inferred← citeshttps://doi.org/10.1002/ejoc.202400032openalex-snapshot
Pd‐Catalyzed Synthesis of Aryl Esters Involving Difluorocarbene Transfer Carbonylation
inferred← citeshttps://doi.org/10.1002/hlca.201900097openalex-snapshot
A Concise Synthesis ofrac‐Ambrox®viathe Palladium(0)‐Catalyzed Carboalkoxylation of an Allylic Ammonium Salt, as Compared to a Formaldehyde HeteroDiels–AlderApproach
inferred← citeshttps://doi.org/10.1002/slct.202300871openalex-snapshot
A Facile synthesis of Biaryl ketones in recyclable system: Triazenes as new coupling partners in the carbonylative Suzuki and Hiyama cross‐coupling reactions using NFSac as CO source
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
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Quaternary ammonium salts on textile coatings and surfaces: structure, preparation, and antibacterial functionalization—a review
inferred← citeshttps://doi.org/10.1007/s41061-019-0239-2openalex-snapshot
Quaternary Ammonium Compounds: Simple in Structure, Complex in Application
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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
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The lower the better: Efficient carbonylative reactions under atmospheric pressure of carbon monoxide
inferred← citeshttps://doi.org/10.1016/j.gresc.2021.04.005openalex-snapshot
Transition-metal-catalyzed transformations of C–N single bonds: Advances in the last five years, challenges and prospects
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2024.110328openalex-snapshot
Potassium hexafluorotitanate as a catalytic activator for direct amidation of carboxylic acids
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131262openalex-snapshot
Synthesis of α-ketoamides using potassium superoxide (KO2) as an oxidizing agent
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132431openalex-snapshot
C(sp2)-C(sp2) Suzuki cross-coupling of arylammonium salts catalyzed by a stable Pd–NHC complex
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00685openalex-snapshot
Manganese(I) Catalyzed α-Alkenylation of Amides Using Alcohols with Liberation of Hydrogen and Water
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01339openalex-snapshot
Palladium-Catalyzed Stereoselective Difunctionalization of Bicyclic Alkenes with Organoammonium Salts and Organoboronic Compounds
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01288openalex-snapshot
Amine Activation: “Inverse” Dipeptide Synthesis and Amide Function Formation through Activated Amino Compounds
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02093openalex-snapshot
Bifunctional 1,8-Diazabicyclo[5.4.0]undec-7-ene for Visible Light-Induced Heck-Type Perfluoroalkylation of Alkenes
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00947openalex-snapshot
Phototriggered Generation of Ynol Ethers and Their Rearrangement to Ketenes
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01877openalex-snapshot
Palladium-Catalyzed Coupling of Terminal Alkynes with Benzyl Ammonium Salts
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01284openalex-snapshot
Nickel-Catalyzed Formal Aminocarbonylation of Secondary Benzyl Chlorides with Isocyanides
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02631openalex-snapshot
Palladium-Catalyzed Decarboxylative Carbonylative Transformation of Benzyl Aryl Carbonates: Direct Synthesis of Aryl 2-Arylacetates
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02820openalex-snapshot
Palladium-Catalyzed Highly Regioselective Aromatic Substitution of Benzylic Ammonium Salts with Amines
inferred← citeshttps://doi.org/10.1021/acscatal.0c01479openalex-snapshot
No Making Without Breaking: Nitrogen-Centered Carbonylation Reactions
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/10.1039/c9ob02667copenalex-snapshot
Chemical transformations of quaternary ammonium salts via C–N bond cleavage
inferred← citeshttps://doi.org/10.1039/d0ob01807dopenalex-snapshot
Reframing primary alkyl amines as aliphatic building blocks
inferred← citeshttps://doi.org/10.1039/d0qo00854kopenalex-snapshot
Palladium-catalyzed carbonylative synthesis of arylacetamides from benzyl formates and tertiary amines
inferred← citeshttps://doi.org/10.1098/rsos.181389openalex-snapshot
ROTf-induced annulation of heteroatom reagents and unsaturated substrates leading to cyclic compounds
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Koruyucu Yardımcı Maddeler Olarak Kullanılan Parabenin Yeni Türevlerinin Sentezi Ve Antimikrobiyal Etkilerinin İncelenmesi
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Borane-Pyridine: An Efficient Catalyst for Direct Amidation
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Advances in Formation of C—X Bonds via Cleavage of C—N Bond of Quaternary Ammonium Salts
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Research Progress on Carbonylation Involving Name Reactions
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Autotransfert d’hydrogène catalysé par du nickel hétérogène pour la formation de liaisons C-C et C-N
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