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Metal-catalyzed activation of ethers via C–O bond cleavage: a new strategy for molecular diversity

https://doi.org/10.1039/c4cs00206g
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What this work says

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

inferredcites →https://doi.org/10.1002/3527601767openalex-snapshot
Modern Arene Chemistry
inferredcites →https://doi.org/10.1002/3527606548openalex-snapshot
Boronic Acids
inferredcites →https://doi.org/10.1002/adsc.200505158openalex-snapshot
Industrial‐Scale Palladium‐Catalyzed Coupling of Aryl Halides and Amines –A Personal Account
inferredcites →https://doi.org/10.1002/ange.200907287openalex-snapshot
Nickel‐Catalyzed Amination of Aryl Pivalates by the Cleavage of Aryl CO Bonds
inferredcites →https://doi.org/10.1002/anie.198709721openalex-snapshot
Ether Cleavage with Organo‐Alkali‐Metal Compounds and Alkali Metals
inferredcites →https://doi.org/10.1002/anie.199706251openalex-snapshot
Selective Activation of Alkyl– and Aryl–Oxygen Single Bonds in Solution with Transition Metal Complexes
inferredcites →https://doi.org/10.1002/anie.200300579openalex-snapshot
Highly Functionalized Organomagnesium Reagents Prepared through Halogen–Metal Exchange
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.200453765openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of Aryl Grignard Reagents with Aromatic Alkyl Ethers: An Efficient Synthesis of Unsymmetrical Biaryls
inferredcites →https://doi.org/10.1002/anie.200461189openalex-snapshot
Monoligated Palladium Species as Catalysts in Cross‐Coupling Reactions
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.200500368openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling Reactions in Total Synthesis
inferredcites →https://doi.org/10.1002/anie.200601663openalex-snapshot
Palladium Complexes of N‐Heterocyclic Carbenes as Catalysts for Cross‐Coupling Reactions—A Synthetic Chemist's Perspective
inferredcites →https://doi.org/10.1002/anie.200604369openalex-snapshot
Deprotonative Metalation Using Ate Compounds: Synergy, Synthesis, and Structure Building
inferredcites →https://doi.org/10.1002/anie.200800497openalex-snapshot
Biaryl Phosphane Ligands in Palladium‐Catalyzed Amination
inferredcites →https://doi.org/10.1002/anie.200801447openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of Aryl Methyl Ethers with Aryl Boronic Esters
inferredcites →https://doi.org/10.1002/anie.200907287openalex-snapshot
Nickel‐Catalyzed Amination of Aryl Pivalates by the Cleavage of Aryl CO Bonds
inferredcites →https://doi.org/10.1002/anie.201001865openalex-snapshot
The Measure of All Rings—N‐Heterocyclic Carbenes
inferredcites →https://doi.org/10.1002/anie.201006139openalex-snapshot
Removable Directing Groups in Organic Synthesis and Catalysis
inferredcites →https://doi.org/10.1002/anie.201202527openalex-snapshot
Synthesis of Enantioenriched Triarylmethanes by Stereospecific Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/anie.201208843openalex-snapshot
Nickel‐Catalyzed Decarbonylative CH Coupling Reactions: A Strategy for Preparing Bis(heteroaryl) Backbones
inferredcites →https://doi.org/10.1002/anie.201304492openalex-snapshot
CH Alkenylation of Azoles with Enols and Esters by Nickel Catalysis
inferredcites →https://doi.org/10.1002/anie.201305342openalex-snapshot
Selective Reductive Cleavage of Inert Aryl CO Bonds by an Iron Catalyst
inferredcites →https://doi.org/10.1002/anie.201308666openalex-snapshot
Stereospecific Nickel‐Catalyzed Cross‐Coupling Reactions of Alkyl Grignard Reagents and Identification of Selective Anti‐Breast‐Cancer Agents
inferredcites →https://doi.org/10.1002/anie.201403823openalex-snapshot
Nickel‐Catalyzed α‐Arylation of Ketones with Phenol Derivatives
inferredcites →https://doi.org/10.1002/cctc.201100087openalex-snapshot
Alkoxy–Arene Cleavage using Ni Catalysts
inferredcites →https://doi.org/10.1002/cctc.201100181openalex-snapshot
Catalytic Hydrogenolysis of CO Bonds in Aryl Ethers
inferredcites →https://doi.org/10.1002/chem.201001022openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of Non‐Activated or Functionalized Aryl Halides with Aryl Grignard Reagents
inferredcites →https://doi.org/10.1002/chem.201002273openalex-snapshot
Activation of “Inert” Alkenyl/Aryl CO Bond and Its Application in Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/chem.201003731openalex-snapshot
Cross‐Coupling of Aryl/Alkenyl Ethers with Aryl Grignard Reagents through Nickel‐Catalyzed CO Activation
inferredcites →https://doi.org/10.1002/chem.201103784openalex-snapshot
Aryl Ether as a Negishi Coupling Partner: An Approach for Constructing CC Bonds under Mild Conditions
inferredcites →https://doi.org/10.1002/chem.201402302openalex-snapshot
Reductive Cross‐Coupling Reactions between Two Electrophiles
inferredcites →https://doi.org/10.1002/chem.201402509openalex-snapshot
Metal‐Catalyzed Reductive Coupling Reactions of Organic Halides with Carbonyl‐Type Compounds
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Recent Progress in Nickel‐Catalyzed Biaryl Coupling
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Catalytic Transformations Involving the Activation of sp2 Carbon–Oxygen Bonds
inferredcites →https://doi.org/10.1007/978-94-009-4099-4openalex-snapshot
Thermochemical Data of Organic Compounds
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1,2-metallate rearrangements: stannyl and (stannyl)vinyl transfers
inferredcites →https://doi.org/10.1016/j.ccr.2004.09.014openalex-snapshot
Copper in cross-coupling reactions
inferredcites →https://doi.org/10.1016/j.tet.2003.08.009openalex-snapshot
Regioselective reductive demethoxylation of 3,4,5-trimethoxystilbenes
inferredcites →https://doi.org/10.1016/j.tet.2012.04.005openalex-snapshot
Ni(0)/NHC-catalyzed amination of N-heteroaryl methyl ethers through the cleavage of carbon‒oxygen bonds
inferredcites →https://doi.org/10.1016/s0040-4020(02)01188-2openalex-snapshot
Recent applications of the Suzuki–Miyaura cross-coupling reaction in organic synthesis
inferredcites →https://doi.org/10.1016/s0040-4039(01)95429-2openalex-snapshot
A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides
inferredcites →https://doi.org/10.1021/ar0201106openalex-snapshot
Palladium-Catalyzed α-Arylation of Carbonyl Compounds and Nitriles
inferredcites →https://doi.org/10.1021/ar100082dopenalex-snapshot
Exploration of New C−O Electrophiles in Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/ar800036sopenalex-snapshot
Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands
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/ar800254yopenalex-snapshot
Avant-Garde Metalating Agents: Structural Basis of Alkali-Metal-Mediated Metalation
inferredcites →https://doi.org/10.1021/cr00039a007openalex-snapshot
Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
inferredcites →https://doi.org/10.1021/cr00089a009openalex-snapshot
Monomeric metal hydroxides, alkoxides, and amides of the late transition metals: synthesis, reactions, and thermochemistry
inferredcites →https://doi.org/10.1021/cr100259topenalex-snapshot
Nickel-Catalyzed Cross-Couplings Involving Carbon−Oxygen Bonds
inferredcites →https://doi.org/10.1021/cr960118ropenalex-snapshot
Cyclometalated Phosphine-Based Pincer Complexes: Mechanistic Insight in Catalysis, Coordination, and Bond Activation
inferredcites →https://doi.org/10.1021/cr9903048openalex-snapshot
The Heck Reaction as a Sharpening Stone of Palladium Catalysis
inferredcites →https://doi.org/10.1021/ic061926wopenalex-snapshot
Electronic Effects on Reductive Elimination To Form Carbon−Carbon and Carbon−Heteroatom Bonds from Palladium(II) Complexes
inferredcites →https://doi.org/10.1021/ja00205a013openalex-snapshot
Electron-spin distribution in radical anions of aryl methyl ethers vs reactivity and regioselectivity of their unimolecular fragmentation
inferredcites →https://doi.org/10.1021/ja00502a074openalex-snapshot
Nickel-induced conversion of carbon-oxygen into carbon-carbon bonds. One-step transformations of enol ethers into olefins and aryl ethers into biaryls
inferredcites →https://doi.org/10.1021/ja00767a075openalex-snapshot
Selective carbon-carbon bond formation by cross-coupling of Grignard reagents with organic halides. Catalysis by nickel-phosphine complexes
inferredcites →https://doi.org/10.1021/ja01304a040openalex-snapshot
Hydrogenation and Hydrogenolysis of Ethers
inferredcites →https://doi.org/10.1021/ja0393170openalex-snapshot
Ruthenium-Catalyzed Functionalization of Aryl Carbon−Oxygen Bonds in Aromatic Ethers with Organoboron Compounds
inferredcites →https://doi.org/10.1021/ja067612popenalex-snapshot
Direct Observation of the Oxidative Addition of the Aryl Carbon−Oxygen Bond to a Ruthenium Complex and Consideration of the Relative Reactivity between Aryl Carbon−Oxygen and Aryl Carbon−Hydrogen Bonds
inferredcites →https://doi.org/10.1021/ja101186popenalex-snapshot
Nickel-Catalyzed Allylic Substitution of Simple Alkenes
inferredcites →https://doi.org/10.1021/ja1052329openalex-snapshot
Arrested 1,2-Hydrogen Migration from Silicon to Nickel upon Oxidation of a Three-Coordinate Ni(I) Silyl Complex
inferredcites →https://doi.org/10.1021/ja108547uopenalex-snapshot
Stereospecific Nickel-Catalyzed Cross-Coupling Reactions of Alkyl Ethers: Enantioselective Synthesis of Diarylethanes
inferredcites →https://doi.org/10.1021/ja205824qopenalex-snapshot
Hydrogenolysis of Palladium(II) Hydroxide, Phenoxide, and Alkoxide Complexes
inferredcites →https://doi.org/10.1021/ja210249hopenalex-snapshot
Nickel-Catalyzed C–H/C–O Coupling of Azoles with Phenol Derivatives
inferredcites →https://doi.org/10.1021/ja300326topenalex-snapshot
Nickel-Mediated Hydrogenolysis of C–O Bonds of Aryl Ethers: What Is the Source of the Hydrogen?
inferredcites →https://doi.org/10.1021/ja3085912openalex-snapshot
A Heterogeneous Nickel Catalyst for the Hydrogenolysis of Aryl Ethers without Arene Hydrogenation
inferredcites →https://doi.org/10.1021/ja309915eopenalex-snapshot
Ni-Catalyzed Cleavage of Aryl Ethers in the Aqueous Phase
inferredcites →https://doi.org/10.1021/ja311940sopenalex-snapshot
Combined Experimental and Theoretical Study on the Reductive Cleavage of Inert C–O Bonds with Silanes: Ruling out a Classical Ni(0)/Ni(II) Catalytic Couple and Evidence for Ni(I) Intermediates
inferredcites →https://doi.org/10.1021/ja312464bopenalex-snapshot
Cleavage of Ether, Ester, and Tosylate C(sp3)–O Bonds by an Iridium Complex, Initiated by Oxidative Addition of C–H Bonds. Experimental and Computational Studies
inferredcites →https://doi.org/10.1021/ja410883popenalex-snapshot
Ni-Catalyzed Carboxylation of C(sp2)– and C(sp3)–O Bonds with CO2
inferredcites →https://doi.org/10.1021/ja412107bopenalex-snapshot
A Mild Ni/Cu-Catalyzed Silylation via C – O Cleavage
inferredcites →https://doi.org/10.1021/ja5026485openalex-snapshot
Enantiospecific Intramolecular Heck Reactions of Secondary Benzylic Ethers
inferredcites →https://doi.org/10.1021/ja5029793openalex-snapshot
Ni-Catalyzed Direct Reductive Amidation via C–O Bond Cleavage
inferredcites →https://doi.org/10.1021/ja5043534openalex-snapshot
Diarylrhodates as Promising Active Catalysts for the Arylation of Vinyl Ethers with Grignard Reagents
inferredcites →https://doi.org/10.1021/ja710944jopenalex-snapshot
Direct Benzylic Alkylation via Ni-Catalyzed Selective Benzylic sp3 C−O Activation
inferredcites →https://doi.org/10.1021/ja8056503openalex-snapshot
Biaryl Construction via Ni-Catalyzed C−O Activation of Phenolic Carboxylates
inferredcites →https://doi.org/10.1021/ja806244bopenalex-snapshot
Cross-Coupling Reactions of Aryl Pivalates with Boronic Acids
inferredcites →https://doi.org/10.1021/ja807936qopenalex-snapshot
Hydrogenolysis of Palladium(II) Hydroxide and Methoxide Pincer Complexes
inferredcites →https://doi.org/10.1021/ja906930uopenalex-snapshot
Cleavage of sp3 C−O Bonds via Oxidative Addition of C−H Bonds
inferredcites →https://doi.org/10.1021/ja9738889openalex-snapshot
Alkyl− and Aryl−Oxygen Bond Activation in Solution by Rhodium(I), Palladium(II), and Nickel(II). Transition-Metal-Based Selectivity
inferredcites →https://doi.org/10.1021/jo00199a030openalex-snapshot
Transformation of carbon-oxygen into carbon-carbon bonds mediated by low-valent nickel species
inferredcites →https://doi.org/10.1021/jo00979a024openalex-snapshot
Palladium-catalyzed vinylic hydrogen substitution reactions with aryl, benzyl, and styryl halides
inferredcites →https://doi.org/10.1021/jo991059vopenalex-snapshot
Electrostatic and Electrophilic Catalysis in the Reductive Cleavage of Alkyl Aryl Ethers. The Influence of Ion Pairing on the Regioselectivity
inferredcites →https://doi.org/10.1021/ol203322vopenalex-snapshot
Nickel(0)-Catalyzed Heck Cross-Coupling via Activation of Aryl C–OPiv Bonds
inferredcites →https://doi.org/10.1021/ol300891kopenalex-snapshot
Traceless Directing Group for Stereospecific Nickel-Catalyzed Alkyl−Alkyl Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/ol302112qopenalex-snapshot
Kumada–Tamao–Corriu Coupling of Heteroaromatic Chlorides and Aryl Ethers Catalyzed by (IPr)Ni(allyl)Cl
inferredcites →https://doi.org/10.1021/ol4011757openalex-snapshot
Programmed Selective sp2 C–O Bond Activation toward Multiarylated Benzenes
inferredcites →https://doi.org/10.1021/ol4014238openalex-snapshot
Sequential Retro-Ene Arylation Reaction of N-Alkoxyenamides for the Synthesis of tert-Alkylamines
inferredcites →https://doi.org/10.1021/ol4031815openalex-snapshot
Ni-Catalyzed Stereoselective Arylation of Inert C–O bonds at Low Temperatures
inferredcites →https://doi.org/10.1021/ol901217mopenalex-snapshot
Carbon−Carbon Formation via Ni-Catalyzed Suzuki−Miyaura Coupling through C−CN Bond Cleavage of Aryl Nitrile
inferredcites →https://doi.org/10.1021/ol9017613openalex-snapshot
A Nickel Catalyst for the Addition of Organoboronate Esters to Ketones and Aldehydes
inferredcites →https://doi.org/10.1021/ol901978eopenalex-snapshot
Nickel-Catalyzed Cross-Coupling Reaction of Alkenyl Methyl Ethers with Aryl Boronic Esters
inferredcites →https://doi.org/10.1021/om00128a009openalex-snapshot
Reactivity of formaldehyde and acetaldehyde toward [N(CH2CH2PPh2)3]Ni and [N(CH2CH2PPh2)3]CoH
inferredcites →https://doi.org/10.1021/om00143a005openalex-snapshot
Metal-formaldehyde chemistry: metal-promoted elementary transformations of formaldehyde
inferredcites →https://doi.org/10.1021/om900400sopenalex-snapshot
Decomposition of Methylnickel(II) Amido, Alkoxo, and Alkyl Complexes by β-Hydrogen Elimination: A Comparative Study
inferredcites →https://doi.org/10.1021/op025620uopenalex-snapshot
The Synthesis of OSU 6162: Efficient, Large-Scale Implementation of a Suzuki Coupling
inferredcites →https://doi.org/10.1038/366529a0openalex-snapshot
Efficient catalytic addition of aromatic carbon-hydrogen bonds to olefins
inferredcites →https://doi.org/10.1039/b314042copenalex-snapshot
Recent developments in the synthetic and structural chemistry of lithium zincates
inferredcites →https://doi.org/10.1039/b718998bopenalex-snapshot
Methylation of arenes via Ni-catalyzed aryl C–O/F activation
inferredcites →https://doi.org/10.1039/b903646fopenalex-snapshot
Sterically demanding trialkylphosphines for palladium-catalyzed cross coupling reactions—alternatives to PtBu3
inferredcites →https://doi.org/10.1039/c0cc05169aopenalex-snapshot
Nickel-catalyzed reductive cleavage of aryl–oxygen bonds in alkoxy- and pivaloxyarenes using hydrosilanes as a mild reducing agent
inferredcites →https://doi.org/10.1039/c0sc00331jopenalex-snapshot
Dialkylbiaryl phosphines in Pd-catalyzed amination: a user's guide
inferredcites →https://doi.org/10.1039/c2sc21657dopenalex-snapshot
Cleavage and hydrodeoxygenation (HDO) of C–O bonds relevant to lignin conversion using Pd/Zn synergistic catalysis
inferredcites →https://doi.org/10.1039/c3972000144aopenalex-snapshot
Activation of Grignard reagents by transition-metal complexes. A new and simple synthesis of trans-stilbenes and polyphenyls
inferredcites →https://doi.org/10.1039/c39790000866openalex-snapshot
Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst
inferredcites →https://doi.org/10.1039/c39840000617openalex-snapshot
A synthesis of conjugated dienes from aromatic, five-membered heterocycles
inferredcites →https://doi.org/10.1039/c3cc43616kopenalex-snapshot
Fe-promoted cross coupling of homobenzylic methyl ethers with Grignard reagents via sp3 C–O bond cleavage
inferredcites →https://doi.org/10.1039/c3cs35521gopenalex-snapshot
Transition-metal-catalyzed Suzuki–Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts
inferredcites →https://doi.org/10.1039/c3sc22256jopenalex-snapshot
Lewis-base silane activation: from reductive cleavage of aryl ethers to selective ortho-silylation
inferredcites →https://doi.org/10.1126/science.1200437openalex-snapshot
Selective, Nickel-Catalyzed Hydrogenolysis of Aryl Ethers
inferredcites →https://doi.org/10.1139/cjc-77-7-1225openalex-snapshot
Electrocatalytic hydrogenation of 4-phenoxyphenol on active powders highly dispersed in a reticulated vitreous carbon electrode
inferredcites →https://doi.org/10.1246/bcsj.44.581openalex-snapshot
Arylation of Olefin with Aryl Iodide Catalyzed by Palladium
inferredcites →https://doi.org/10.1246/cl.2009.710openalex-snapshot
Ni0-catalyzed Direct Amination of Anisoles Involving the Cleavage of Carbon–Oxygen Bonds

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/ange.201412051openalex-snapshot
Nickel‐Catalyzed Enantioselective CC Bond Formation through CO Cleavage in Aryl Esters
inferred← citeshttps://doi.org/10.1002/ange.201412249openalex-snapshot
Organoaluminum‐Mediated Direct Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/ange.201412319openalex-snapshot
C‐H‐Alkenylierungen mit Alkenylacetaten, ‐phosphaten, ‐carbonaten und ‐carbamaten durch Cobalt‐Katalyse bei 23 °C
inferred← citeshttps://doi.org/10.1002/ange.201503204openalex-snapshot
Nickelkatalysierte C‐O/C‐H‐Kreuzkupplungen zur C‐C‐Bindungsbildung
inferred← citeshttps://doi.org/10.1002/ange.201503641openalex-snapshot
Ruthenium‐Catalyzed Monoalkenylation of Aromatic Ketones by Cleavage of Carbon–Heteroatom Bonds with Unconventional Chemoselectivity
inferred← citeshttps://doi.org/10.1002/ange.201504524openalex-snapshot
Iron‐Catalyzed Cross‐Coupling of Alkenyl Acetates
inferred← citeshttps://doi.org/10.1002/ange.201506751openalex-snapshot
Formal Direct Cross‐Coupling of Phenols with Amines
inferred← citeshttps://doi.org/10.1002/ange.201509133openalex-snapshot
Chemo‐ and Regioselective Hydrogenolysis of Diaryl Ether C−O Bonds by a Robust Heterogeneous Ni/C Catalyst: Applications to the Cleavage of Complex Lignin‐Related Fragments
inferred← citeshttps://doi.org/10.1002/ange.201510497openalex-snapshot
Lewis‐Säure‐unterstützte metallkatalysierte Kreuzkupplung: Alkylierung von Arylmethylethern unter C‐O‐Bindungsspaltung ohne β‐Hydrideliminierung
inferred← citeshttps://doi.org/10.1002/ange.201601914openalex-snapshot
Synthesis of Biaryls through Nickel‐Catalyzed Suzuki–Miyaura Coupling of Amides by Carbon–Nitrogen Bond Cleavage
inferred← citeshttps://doi.org/10.1002/ange.201602095openalex-snapshot
Lactamization of sp2 C−H Bonds with CO2: Transition‐Metal‐Free and Redox‐Neutral
inferred← citeshttps://doi.org/10.1002/ange.201607646openalex-snapshot
Nickel‐katalysierter Alkoxy‐Alkyl‐Austausch mit Alkylboranen mittels C‐O‐Aktivierung von Aryl‐ und Enolethern
inferred← citeshttps://doi.org/10.1002/ange.201610203openalex-snapshot
NHC‐organokatalysierte CAr‐O‐Bindungsspaltung: milder Zugang zu 2‐Hydroxybenzophenonen
inferred← citeshttps://doi.org/10.1002/ange.201610409openalex-snapshot
C−O Activation by a Rhodium Bis(N‐Heterocyclic Carbene) Catalyst: Aryl Carbamates as Arylating Reagents in Directed C−H Arylation
inferred← citeshttps://doi.org/10.1002/ange.201611720openalex-snapshot
Ni‐Catalyzed Stannylation of Aryl Esters via C−O Bond Cleavage
inferred← citeshttps://doi.org/10.1002/ange.201702188openalex-snapshot
Bildung von C‐C‐Bindungen durch Decarbonylierung von Arylketonen
inferred← citeshttps://doi.org/10.1002/ange.201702857openalex-snapshot
Switchable Site‐Selective Catalytic Carboxylation of Allylic Alcohols with CO2
inferred← citeshttps://doi.org/10.1002/ange.201706597openalex-snapshot
Efficient Aryl Migration from an Aryl Ether to a Carboxylic Acid Group To Form an Ester by Visible‐Light Photoredox Catalysis
inferred← citeshttps://doi.org/10.1002/ange.201802563openalex-snapshot
Eisenkatalysierte C‐O/C‐O‐Bindungsmetathese von aliphatischen Ethern
inferred← citeshttps://doi.org/10.1002/ange.201803186openalex-snapshot
Übergangsmetallkatalysierte Carboxylierungen mit Kohlendioxid
inferred← citeshttps://doi.org/10.1002/ange.201805927openalex-snapshot
Synergistic Catalysis for the Umpolung Trifluoromethylthiolation of Tertiary Ethers
inferred← citeshttps://doi.org/10.1002/ange.201806790openalex-snapshot
Nickel‐Catalyzed Amination of Silyloxyarenes through C–O Bond Activation
inferred← citeshttps://doi.org/10.1002/ange.201909551openalex-snapshot
The Critical Role of Reductive Steps in the Nickel‐Catalyzed Hydrogenolysis and Hydrolysis of Aryl Ether C−O Bonds
inferred← citeshttps://doi.org/10.1002/ange.201911372openalex-snapshot
Nickel‐Catalyzed Domino Heck‐Type Reactions Using Methyl Esters as Cross‐Coupling Electrophiles
inferred← citeshttps://doi.org/10.1002/ange.202001571openalex-snapshot
Alkyl Carbazates for Electrochemical Deoxygenative Functionalization of Heteroarenes
inferred← citeshttps://doi.org/10.1002/ange.202004116openalex-snapshot
Nickel‐Mediated Trifluoromethylation of Phenol Derivatives by Aryl C−O Bond Activation
inferred← citeshttps://doi.org/10.1002/ange.202006740openalex-snapshot
Transformations of Aryl Ketones via Ligand‐Promoted C−C Bond Activation
inferred← citeshttps://doi.org/10.1002/ange.202103327openalex-snapshot
Direct Synthesis of Ketones from Methyl Esters by Nickel‐Catalyzed Suzuki–Miyaura Coupling
inferred← citeshttps://doi.org/10.1002/ange.202201329openalex-snapshot
Dehydroxylative Alkylation of α‐Hydroxy Carboxylic Acid Derivatives via a Spin‐Center Shift
inferred← citeshttps://doi.org/10.1002/ange.202210132openalex-snapshot
Silicon Catalyzed C−O Bond Ring Closing Metathesis of Polyethers
inferred← citeshttps://doi.org/10.1002/ange.202210484openalex-snapshot
Carbonylative Cross‐Coupling Reaction of Allylic Alcohols and Organoalanes with 1 atm CO Enabled by Nickel Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202306581openalex-snapshot
Catalytic σ‐Bond Annulation with Ambiphilic Organohalides Enabled by β‐X Elimination**
inferred← citeshttps://doi.org/10.1002/ange.202401756openalex-snapshot
Nickel‐Catalyzed Chemoselective Carbomagnesiation for Atroposelective Ring‐Opening Difunctionalization
inferred← citeshttps://doi.org/10.1002/ange.202413374openalex-snapshot
Carbonylation Reactions at Carbon‐Centered Radicals with an Adjacent Heteroatom
inferred← citeshttps://doi.org/10.1002/ange.202424186openalex-snapshot
Mechanochemically Enabled Formal Reductive Cross‐Coupling Reaction Between Aryl Ethers and Aryl Fluorides
inferred← citeshttps://doi.org/10.1002/ange.202501767openalex-snapshot
Regiodivergent and Enantioselective Hydroboration of Dienol Ethers
inferred← citeshttps://doi.org/10.1002/ange.202505028openalex-snapshot
Rhodium/Indium Heterobimetallic Alloy as an Effective Catalyst for Reductive C(sp 3 )─O Silylation of Ethers with Chlorosilanes
inferred← citeshttps://doi.org/10.1002/ange.202518631openalex-snapshot
Magnesiation of Phenol Derivatives Catalyzed by a Rhodium─Aluminum Complex
inferred← citeshttps://doi.org/10.1002/ange.202520176openalex-snapshot
Cobalt‐Catalyzed Deoxygenative Coupling of Ethers to Alkanes
inferred← citeshttps://doi.org/10.1002/ange.2984592openalex-snapshot
Atroposelective Dearomative Cross‐Coupling of Benzofuran Derivatives by Z‐Selective Functionalization of the Vinyl C─O Bond
inferred← citeshttps://doi.org/10.1002/ange.4827662openalex-snapshot
Photoredox Conversion of Phenol Derivatives Into β ‐Arylpropionic Acids via Radical 1,4‐Aryl Migration
inferred← citeshttps://doi.org/10.1002/ange.9495829openalex-snapshot
Deoxygenative Functionalization of Unprotected Phenols by Linear Paired Electrolysis
inferred← citeshttps://doi.org/10.1002/anie.201412051openalex-snapshot
Nickel‐Catalyzed Enantioselective CC Bond Formation through CO Cleavage in Aryl Esters
inferred← citeshttps://doi.org/10.1002/anie.201412249openalex-snapshot
Organoaluminum‐Mediated Direct Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/anie.201412319openalex-snapshot
CH Alkenylations with Alkenyl Acetates, Phosphates, Carbonates, and Carbamates by Cobalt Catalysis at 23 °C
inferred← citeshttps://doi.org/10.1002/anie.201503204openalex-snapshot
Nickel‐Catalyzed CO/CH Cross‐Coupling Reactions for CC Bond Formation
inferred← citeshttps://doi.org/10.1002/anie.201503641openalex-snapshot
Ruthenium‐Catalyzed Monoalkenylation of Aromatic Ketones by Cleavage of Carbon–Heteroatom Bonds with Unconventional Chemoselectivity
inferred← citeshttps://doi.org/10.1002/anie.201504524openalex-snapshot
Iron‐Catalyzed Cross‐Coupling of Alkenyl Acetates
inferred← citeshttps://doi.org/10.1002/anie.201506751openalex-snapshot
Formal Direct Cross‐Coupling of Phenols with Amines
inferred← citeshttps://doi.org/10.1002/anie.201509133openalex-snapshot
Chemo‐ and Regioselective Hydrogenolysis of Diaryl Ether C−O Bonds by a Robust Heterogeneous Ni/C Catalyst: Applications to the Cleavage of Complex Lignin‐Related Fragments
inferred← citeshttps://doi.org/10.1002/anie.201510497openalex-snapshot
Lewis Acid Assisted Nickel‐Catalyzed Cross‐Coupling of Aryl Methyl Ethers by C−O Bond‐Cleaving Alkylation: Prevention of Undesired β‐Hydride Elimination
inferred← citeshttps://doi.org/10.1002/anie.201601914openalex-snapshot
Synthesis of Biaryls through Nickel‐Catalyzed Suzuki–Miyaura Coupling of Amides by Carbon–Nitrogen Bond Cleavage
inferred← citeshttps://doi.org/10.1002/anie.201602095openalex-snapshot
Lactamization of sp 2 C−H Bonds with CO 2 : Transition‐Metal‐Free and Redox‐Neutral
inferred← citeshttps://doi.org/10.1002/anie.201607646openalex-snapshot
Nickel‐Catalyzed Alkoxy–Alkyl Interconversion with Alkylborane Reagents through C−O Bond Activation of Aryl and Enol Ethers
inferred← citeshttps://doi.org/10.1002/anie.201610203openalex-snapshot
NHC‐Organocatalyzed C Ar −O Bond Cleavage: Mild Access to 2‐Hydroxybenzophenones
inferred← citeshttps://doi.org/10.1002/anie.201610409openalex-snapshot
C−O Activation by a Rhodium Bis(N‐Heterocyclic Carbene) Catalyst: Aryl Carbamates as Arylating Reagents in Directed C−H Arylation
inferred← citeshttps://doi.org/10.1002/anie.201611720openalex-snapshot
Ni‐Catalyzed Stannylation of Aryl Esters via C−O Bond Cleavage
inferred← citeshttps://doi.org/10.1002/anie.201702188openalex-snapshot
Forging C−C Bonds Through Decarbonylation of Aryl Ketones
inferred← citeshttps://doi.org/10.1002/anie.201702857openalex-snapshot
Switchable Site‐Selective Catalytic Carboxylation of Allylic Alcohols with CO2
inferred← citeshttps://doi.org/10.1002/anie.201706597openalex-snapshot
Efficient Aryl Migration from an Aryl Ether to a Carboxylic Acid Group To Form an Ester by Visible‐Light Photoredox Catalysis
inferred← citeshttps://doi.org/10.1002/anie.201802563openalex-snapshot
Iron‐Catalyzed Ring‐Closing C−O/C−O Metathesis of Aliphatic Ethers
inferred← citeshttps://doi.org/10.1002/anie.201803186openalex-snapshot
Transition‐Metal‐Catalyzed Carboxylation Reactions with Carbon Dioxide
inferred← citeshttps://doi.org/10.1002/anie.201805927openalex-snapshot
Synergistic Catalysis for the Umpolung Trifluoromethylthiolation of Tertiary Ethers
inferred← citeshttps://doi.org/10.1002/anie.201806790openalex-snapshot
Nickel‐Catalyzed Amination of Silyloxyarenes through C–O Bond Activation
inferred← citeshttps://doi.org/10.1002/anie.201909551openalex-snapshot
The Critical Role of Reductive Steps in the Nickel‐Catalyzed Hydrogenolysis and Hydrolysis of Aryl Ether C−O Bonds
inferred← citeshttps://doi.org/10.1002/anie.201911372openalex-snapshot
Nickel‐Catalyzed Domino Heck‐Type Reactions Using Methyl Esters as Cross‐Coupling Electrophiles
inferred← citeshttps://doi.org/10.1002/anie.202001571openalex-snapshot
Alkyl Carbazates for Electrochemical Deoxygenative Functionalization of Heteroarenes
inferred← citeshttps://doi.org/10.1002/anie.202004116openalex-snapshot
Nickel‐Mediated Trifluoromethylation of Phenol Derivatives by Aryl C−O Bond Activation
inferred← citeshttps://doi.org/10.1002/anie.202006740openalex-snapshot
Transformations of Aryl Ketones via Ligand‐Promoted C−C Bond Activation
inferred← citeshttps://doi.org/10.1002/anie.202103327openalex-snapshot
Direct Synthesis of Ketones from Methyl Esters by Nickel‐Catalyzed Suzuki–Miyaura Coupling
inferred← citeshttps://doi.org/10.1002/anie.202201329openalex-snapshot
Dehydroxylative Alkylation of α‐Hydroxy Carboxylic Acid Derivatives via a Spin‐Center Shift
inferred← citeshttps://doi.org/10.1002/anie.202210132openalex-snapshot
Silicon Catalyzed C−O Bond Ring Closing Metathesis of Polyethers
inferred← citeshttps://doi.org/10.1002/anie.202210484openalex-snapshot
Carbonylative Cross‐Coupling Reaction of Allylic Alcohols and Organoalanes with 1 atm CO Enabled by Nickel Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202306581openalex-snapshot
Catalytic σ‐Bond Annulation with Ambiphilic Organohalides Enabled by β‐X Elimination**
inferred← citeshttps://doi.org/10.1002/anie.202401756openalex-snapshot
Nickel‐Catalyzed Chemoselective Carbomagnesiation for Atroposelective Ring‐Opening Difunctionalization
inferred← citeshttps://doi.org/10.1002/anie.202413374openalex-snapshot
Carbonylation Reactions at Carbon‐Centered Radicals with an Adjacent Heteroatom
inferred← citeshttps://doi.org/10.1002/anie.202424186openalex-snapshot
Mechanochemically Enabled Formal Reductive Cross‐Coupling Reaction Between Aryl Ethers and Aryl Fluorides
inferred← citeshttps://doi.org/10.1002/anie.202501767openalex-snapshot
Regiodivergent and Enantioselective Hydroboration of Dienol Ethers
inferred← citeshttps://doi.org/10.1002/anie.202505028openalex-snapshot
Rhodium/Indium Heterobimetallic Alloy as an Effective Catalyst for Reductive C(sp 3 )─O Silylation of Ethers with Chlorosilanes
inferred← citeshttps://doi.org/10.1002/anie.202518631openalex-snapshot
Magnesiation of Phenol Derivatives Catalyzed by a Rhodium─Aluminum Complex
inferred← citeshttps://doi.org/10.1002/anie.202520176openalex-snapshot
Cobalt‐Catalyzed Deoxygenative Coupling of Ethers to Alkanes
inferred← citeshttps://doi.org/10.1002/anie.2984592openalex-snapshot
Atroposelective Dearomative Cross‐Coupling of Benzofuran Derivatives by Z‐Selective Functionalization of the Vinyl C─O Bond
inferred← citeshttps://doi.org/10.1002/anie.4827662openalex-snapshot
Photoredox Conversion of Phenol Derivatives Into β ‐Arylpropionic Acids via Radical 1,4‐Aryl Migration
inferred← citeshttps://doi.org/10.1002/anie.9495829openalex-snapshot
Deoxygenative Functionalization of Unprotected Phenols by Linear Paired Electrolysis
inferred← citeshttps://doi.org/10.1002/aoc.3671openalex-snapshot
Ionic iron(III) complexes bearing a dialkylbenzimidazolium cation: Efficient catalysts for magnesium‐mediated cross‐couplings of aryl phosphates with alkyl bromides
inferred← citeshttps://doi.org/10.1002/asia.201600972openalex-snapshot
Fe‐Catalyzed Cross‐Coupling Reaction of Vinylic Ethers with Aryl Grignard Reagents
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.201701694openalex-snapshot
Copper‐Catalyzed Oxidative Reaction of β‐Keto Sulfones with Alcohols via C−S Bond Cleavage: Reaction Development and Mechanism Study
inferred← citeshttps://doi.org/10.1002/asia.201900330openalex-snapshot
Catalytic Reduction of Cyclic Ethers with Hydrosilanes
inferred← citeshttps://doi.org/10.1002/cctc.201800898openalex-snapshot
Pd‐Ni BMNPs Encapsulated in UiO‐66 as an Efficient Catalyst for the Activation of “Inert” C−O Bonds
inferred← citeshttps://doi.org/10.1002/cctc.202000876openalex-snapshot
Nickel‐Catalyzed Synthesis of N‐(Hetero)aryl Carbamates from Cyanate Salts and Phenols Activated with Cyanuric Chloride
inferred← citeshttps://doi.org/10.1002/cctc.202001347openalex-snapshot
Cobalt−NHC Catalyzed C(sp2)−C(sp3) and C(sp2)−C(sp2) Kumada Cross‐Coupling of Aryl Tosylates with Alkyl and Aryl Grignard Reagents
inferred← citeshttps://doi.org/10.1002/cctc.202300249openalex-snapshot
Coupling of Heteroarene and Arenol via Nickel‐Catalyzed C−H/C−OH Activation
inferred← citeshttps://doi.org/10.1002/cctc.202300589openalex-snapshot
Recent DFT Calculations on the Mechanism of Transition‐Metal‐Catalyzed C−O Activation of Alcohols
inferred← citeshttps://doi.org/10.1002/cctc.202301566openalex-snapshot
Metal‐Catalyzed Enantioselective Cleavage of Aromatic C−O Bonds
inferred← citeshttps://doi.org/10.1002/celc.202400560openalex-snapshot
Electrochemical Borylation of C−C and C−Het Bonds
inferred← citeshttps://doi.org/10.1002/chem.201502114openalex-snapshot
How and Why Does Ni0 Promote Smooth Etheric CO Bond Cleavage and CC Bond Formation? A Theoretical Study
inferred← citeshttps://doi.org/10.1002/chem.201503647openalex-snapshot
Stereospecific Pd‐Catalyzed Intermolecular C(sp3)–C(sp) Cross‐Coupling of Diarylmethyl Carbonates and Terminal Alkynes Under Base‐Free Conditions
inferred← citeshttps://doi.org/10.1002/chem.201504596openalex-snapshot
Chelation‐Assisted Nickel‐Catalyzed Oxidative Annulation via Double C−H Activation/Alkyne Insertion Reaction
inferred← citeshttps://doi.org/10.1002/chem.201504959openalex-snapshot
Exploring Regioselective Bond Cleavage and Cross‐Coupling Reactions using a Low‐Valent Nickel Complex
inferred← citeshttps://doi.org/10.1002/chem.201505106openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of Organolithium Reagents with (Hetero)Aryl Electrophiles
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/chem.201604160openalex-snapshot
Lewis Acid Accelerated Aryl Ether Bond Cleavage with Nickel: Orders of Magnitude Rate Enhancement Using AlMe3
inferred← citeshttps://doi.org/10.1002/chem.201604452openalex-snapshot
Decarboxylative Aminomethylation of Aryl‐ and Vinylsulfonates through Combined Nickel‐ and Photoredox‐Catalyzed Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/chem.201702867openalex-snapshot
Synthesis of Amidines from Amides Using a Nickel‐Catalyzed Decarbonylative Amination through CO Extrusion Intramolecular Recombination Fragment Coupling
inferred← citeshttps://doi.org/10.1002/chem.201703266openalex-snapshot
Mechanistic Study on Nickel‐Catalyzed Silylation of Aryl Methyl Ethers
inferred← citeshttps://doi.org/10.1002/chem.201803451openalex-snapshot
Dismantling of Vinyl Ethers by Pentanuclear [(iPr3P)Ni]5H6: Facile Cooperative C−O, C−C and C−H Activation Pathways
inferred← citeshttps://doi.org/10.1002/chem.201904288openalex-snapshot
Formal Aniline Synthesis from Phenols through Deoxygenative N‐Centered Radical Substitution
inferred← citeshttps://doi.org/10.1002/chem.202004132openalex-snapshot
Directing Group‐Promoted Inert C−O Bond Activation Using Versatile Boronic Acid as a Coupling Agent
inferred← citeshttps://doi.org/10.1002/chem.202200625openalex-snapshot
Nickel‐Catalyzed Csp2−OMe Functionalization for Chemoselective Aromatic Homologation En Route to Nanographenes
inferred← citeshttps://doi.org/10.1002/chem.202302041openalex-snapshot
Visible‐Light Enabled Dehydroxylative Alkylation of α‐Hydroxy Carboxylic Acid Derivatives via C−O Bond Cleavage
inferred← citeshttps://doi.org/10.1002/chem.202303421openalex-snapshot
Metal‐Free, Hindered, Regioselective Access to Multifunctional Groups Diarylamines via SNAr Substitution of P‐Nitroso Aromatic Methyl Ether by Arylamines
inferred← citeshttps://doi.org/10.1002/chem.202500862openalex-snapshot
Ru‐Catalyzed Deoxygenative Functionalization of Phenols via π‐Coordination Activation: Mechanochemical Access to N‐Aryl Amides and α‐Aryl Carbonyls
inferred← citeshttps://doi.org/10.1002/chin.201506274openalex-snapshot
ChemInform Abstract: Metal‐Catalyzed Activation of Ethers via C—O Bond Cleavage: A New Strategy for Molecular Diversity
inferred← citeshttps://doi.org/10.1002/cjoc.201500414openalex-snapshot
Pd‐Catalyzed Synthesis of α‐Aryl Vinylphosphonates via Suzuki Arylation of α‐Phosphonovinyl Nonaflates
inferred← citeshttps://doi.org/10.1002/cjoc.201700664openalex-snapshot
Methylation of Arenols through Ni‐catalyzed C—O Activation with Methyl Magnesium Bromide
inferred← citeshttps://doi.org/10.1002/cjoc.201800554openalex-snapshot
Conversion of Carbonyl Compounds to Olefins via Enolate Intermediate
inferred← citeshttps://doi.org/10.1002/cjoc.201800575openalex-snapshot
Stereoselective Synthesis of Vinylboronates by Rh‐Catalyzed Borylation of Stereoisomeric Mixtures
inferred← citeshttps://doi.org/10.1002/cjoc.201900506openalex-snapshot
Direct Transformation of Arenols Based on C—O Activation
inferred← citeshttps://doi.org/10.1002/cjoc.202200769openalex-snapshot
Reductive Deoxygenative Functionalization of Alcohols by First‐Row Transition Metal Catalysis
inferred← citeshttps://doi.org/10.1002/cjoc.202300096openalex-snapshot
Divergent Synthesis of Organofluorinated Molecules from Titanium Mediated Deoxygenation of Free Alcohols
inferred← citeshttps://doi.org/10.1002/cjoc.202300593openalex-snapshot
Iron‐Catalyzed Reductive C(aryl)—Si Cross‐Coupling of Diaryl Ethers with Chlorosilanes
inferred← citeshttps://doi.org/10.1002/cjoc.70202openalex-snapshot
Electrochemical C–H Functionalization for the Construction of C–O Bonds: A Comprehensive Review
inferred← citeshttps://doi.org/10.1002/cssc.201601293openalex-snapshot
Aromatic Chlorosulfonylation by Photoredox Catalysis
inferred← citeshttps://doi.org/10.1002/cssc.201701287openalex-snapshot
Iron‐Catalyzed C−O Bond Activation: Opportunity for Sustainable Catalysis
inferred← citeshttps://doi.org/10.1002/ejic.201500061openalex-snapshot
Accessible Syntheses of Late Transition Metal (Pre)Catalysts Bearing N‐Heterocyclic Carbene Ligands
inferred← citeshttps://doi.org/10.1002/ejic.201600308openalex-snapshot
Reactivity of [WCl6] with Ethers: A Joint Computational, Spectroscopic and Crystallographic Study
inferred← citeshttps://doi.org/10.1002/ejic.201900513openalex-snapshot
[Cp2Mo(OH)(OH2)]+‐Catalyzed Hydrolysis of Mono‐ and Difunctional Ethers: Theoretical Understanding of Their Divergent Reactivity
inferred← citeshttps://doi.org/10.1002/ejic.201900692openalex-snapshot
Nickel Carbodicarbene Catalyzes Kumada Cross‐Coupling of Aryl Ethers with Grignard Reagents through C–O Bond Activation
inferred← citeshttps://doi.org/10.1002/ejoc.201500226openalex-snapshot
Palladium‐Catalyzed Amination of Aryl Sulfides with Aliphatic Amines
inferred← citeshttps://doi.org/10.1002/ejoc.201500630openalex-snapshot
Nickel‐Catalyzed Decarbonylative Coupling of Aryl Esters and Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/ejoc.201500987openalex-snapshot
Pincer‐Nickel‐Catalyzed Cross‐Coupling of Aryl Sulfamates with Arylzinc Chlorides
inferred← citeshttps://doi.org/10.1002/ejoc.201700514openalex-snapshot
N‐Methylpyrrolidin‐2‐one‐Promoted Formation of Functional Esters through C–O Bond Cleavage
inferred← citeshttps://doi.org/10.1002/ejoc.201701654openalex-snapshot
Iron‐Catalyzed C(sp2)–C(sp3) Cross‐Coupling of Alkyl Grignard Reagents with Polyaromatic Tosylates
inferred← citeshttps://doi.org/10.1002/ejoc.202000071openalex-snapshot
C‐H Functionalization of Biaryl Compounds
inferred← citeshttps://doi.org/10.1002/ejoc.202001342openalex-snapshot
InBr3‐Catalyzed Coupling Reaction between Electron‐Deficient Alkenyl Ethers with Silyl Enolates for Stereoselective Synthesis of 1,5‐Dioxo‐alk‐2‐enes
inferred← citeshttps://doi.org/10.1002/ejoc.202200937openalex-snapshot
Zn‐Mediated Reductive Addition of Isocyanides with Unactivated Tertiary Alkyl Oxalates
inferred← citeshttps://doi.org/10.1002/ejoc.202400376openalex-snapshot
Nickel‐Catalyzed Branch‐Selective C−H Alkylation of Indoles and Azoles with Alkenes: An Additive‐ and Solvent‐Free Approach
inferred← citeshttps://doi.org/10.1002/ejoc.202500615openalex-snapshot
Mechanochemical Nickel‐Catalyzed Suzuki–Miyaura Cross‐Coupling of Phenol‐Derived Cyanate Esters
inferred← citeshttps://doi.org/10.1002/ejoc.70373openalex-snapshot
Catalytic Hydrogenation of Lignin‐Derived Aromatics With Rhodium Oxide in Water
inferred← citeshttps://doi.org/10.1002/jhet.2513openalex-snapshot
Nickel‐catalyzed Kumada Cross‐coupling Reaction for the Synthesis of 2,4‐Diarylquinazolines
inferred← citeshttps://doi.org/10.1002/slct.202100727openalex-snapshot
The Recent Progress on Supported and Recyclable Nickel Catalysts towards Organic Transformations: A Review
inferred← citeshttps://doi.org/10.1002/slct.202101141openalex-snapshot
Copper‐Catalyzed Sonogashira‐Cross‐Coupling of Phenols Using Dichloroimidazolidinedione
inferred← citeshttps://doi.org/10.1002/slct.202103723openalex-snapshot
Mechanism of Ligand‐Controlled Chemoselectivity‐Switchable Ni‐Catalyzed C−N Cross‐Coupling of Amine
inferred← citeshttps://doi.org/10.1002/slct.202505163openalex-snapshot
Dealkylation of Alkyl Aryl Ethers by Potassium Tert‐Amylate
inferred← citeshttps://doi.org/10.1002/tcr.201500305openalex-snapshot
Ni‐Catalyzed Amination Reactions: An Overview
inferred← citeshttps://doi.org/10.1002/tcr.201700069openalex-snapshot
Combination of Tetrabutylammonium Iodide (TBAI) with tert ‐Butyl Hydroperoxide (TBHP): An Efficient Transition‐Metal‐Free System to Construct Various Chemical Bonds
inferred← citeshttps://doi.org/10.1007/3418_2018_19openalex-snapshot
Metal-Catalyzed Aromatic C-O Bond Activation/Transformation
inferred← citeshttps://doi.org/10.1007/3418_2023_91openalex-snapshot
C–C Cross Couplings with Chromium Catalysis
inferred← citeshttps://doi.org/10.1007/978-1-0716-1579-9_13openalex-snapshot
New Directions in Coupling Chemistry
inferred← citeshttps://doi.org/10.1007/s10562-018-2446-9openalex-snapshot
Biomimetic Cleavage of Aryl–Nitrogen Bonds in N-Arylazoles Catalyzed by Metalloporphyrins
inferred← citeshttps://doi.org/10.1007/s11426-023-1589-7openalex-snapshot
Photoinduced difunctionalization with bifunctional reagents containing N-heteroaryl moieties
inferred← citeshttps://doi.org/10.1007/s41061-016-0043-1openalex-snapshot
Nickel-Catalyzed Cross-Coupling Reactions of Unreactive Phenolic Electrophiles via C–O Bond Activation
inferred← citeshttps://doi.org/10.1007/s41061-024-00484-7openalex-snapshot
Recent Advances in C–O Bond Cleavage of Aryl, Vinyl, and Benzylic Ethers
inferred← citeshttps://doi.org/10.1016/b978-0-12-820206-7.00089-5openalex-snapshot
Synthetic Applications of C–O and C–E Bond Activation Reactions
inferred← citeshttps://doi.org/10.1016/bs.acat.2024.05.002openalex-snapshot
Recent advances in Ni-catalyzed functionalization of strong C−O and C−H bonds
inferred← citeshttps://doi.org/10.1016/bs.adomc.2021.04.003openalex-snapshot
Recent progress on group 10 metal complexes of pincer ligands: From synthesis to activities and catalysis
inferred← citeshttps://doi.org/10.1016/bs.adomc.2024.04.002openalex-snapshot
A tale of two metals: The Mizoroki-Heck reaction as a guide to compare the chemical characters of nickel and palladium in catalysis
inferred← citeshttps://doi.org/10.1016/j.apcatb.2019.117936openalex-snapshot
Valorization of wood biomass-lignin via selective bond scission: A minireview
inferred← citeshttps://doi.org/10.1016/j.cclet.2018.09.009openalex-snapshot
Nickel-catalysed C O bond reduction of 2,4,6-triaryloxy-1,3,5-triazines in 2-methyltetrahydrofuran
inferred← citeshttps://doi.org/10.1016/j.cclet.2022.04.026openalex-snapshot
Integrating aryl chlorides into nickel-catalyzed 1,1-difunctionalization of alkenes
inferred← citeshttps://doi.org/10.1016/j.ccr.2015.02.004openalex-snapshot
From models to lignin: Transition metal catalysis for selective bond cleavage reactions
inferred← citeshttps://doi.org/10.1016/j.ccr.2021.214165openalex-snapshot
A new avenue for the preparation of organoboron compounds via nickel catalysis
inferred← citeshttps://doi.org/10.1016/j.cej.2022.137404openalex-snapshot
Controlling reaction pathways via selective C-O activation for highly efficient biomass oriented-upgrading
inferred← citeshttps://doi.org/10.1016/j.checat.2024.101126openalex-snapshot
Cobalt-catalyzed enantioselective hydroetherification of alkenes and symmetric 1,3-diketones
inferred← citeshttps://doi.org/10.1016/j.desal.2026.119879openalex-snapshot
Electrochemically highly selective removal of lead ions from multicomponent water via synergy from covalent organic framework and hollow mesoporous carbon sphere
inferred← citeshttps://doi.org/10.1016/j.gresc.2024.11.003openalex-snapshot
A direct Ni-catalyzed deoxygenative Suzuki-Miyaura cross-coupling reaction of phenols via the formation of active O-phenyluronium
inferred← citeshttps://doi.org/10.1016/j.heliyon.2025.e42431openalex-snapshot
Microwave-assisted synthesis and catalytic activity of nano-sized molybdenum carbide in naphthalene hydrogenation
inferred← citeshttps://doi.org/10.1016/j.ica.2026.123452openalex-snapshot
Nickel-mediated C(sp2)−O bond cleavage: Esters from the coupling of vinyl ethers or the cross-coupling of vinyl ethers with acetaldehyde
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