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Mild and General Palladium-Catalyzed Synthesis of Methyl Aryl Ethers Enabled by the Use of a Palladacycle Precatalyst
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Trideuteriomethoxylation of Aryl and Heteroaryl Halides
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The Selective Reaction of Aryl Halides with KOH: Synthesis of Phenols, Aromatic Ethers, and Benzofurans
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An Improved Cu-Based Catalyst System for the Reactions of Alcohols with Aryl Halides
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One-Step Preparation of Some 3-Substituted Anisoles
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inferredcites →https://doi.org/10.1055/s-1997-722openalex-snapshot
SNAr Bases Macrocyclization via Biaryl Ether Formation: Application in Natural Product Synthesis
inferredcites →https://doi.org/10.1055/s-2007-968010openalex-snapshot
N,N-Dimethylglycine-Promoted Ullmann-Type Coupling Reactions of Aryl Iodides with Aliphatic Alcohols
inferredcites →https://doi.org/10.1080/00397910701316268openalex-snapshot
Solvent‐Free Williamson Synthesis: An Efficient, Simple, and Convenient Method for Chemoselective Etherification of Phenols and Bisphenols
inferredcites →https://doi.org/10.1246/bcsj.20110001openalex-snapshot
Bis(μ-iodo)bis[(−)-sparteine]dicopper: A Versatile Catalyst for Direct O-Arylation and O-Alkylation of Phenols and Aliphatic Alcohols with Haloarenes
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/10.1021/acs.orglett.9b02639openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acscatal.9b03012openalex-snapshot
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Transition-metal free oxidative C–H etherification of acylanilines with alcohols through a radical pathway
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Broadening of horizons in the synthesis of CD 3 -labeled molecules
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A general, versatile and divergent synthesis of selectively deuterated amines
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Catalytic methoxylation of aryl halides using 13 C- and 14 C-labeled CO 2
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Pyridinium-based carboxyl-functionalized porphyrin: an easy gateway to afford substituted benzyl aryl ethers
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Enantioselective copper-catalyzed synthesis of axially chiral deuterated biaryl ethers and phenols from cyclic iodonium salts
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Synthesis of Alkyl Aryl Ethers by O-Arylation of Alcohols with Diaryliodonium Salts: Scope, Limitations, and Mechanism
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Introduction of 4-Chlorophenyl: A Protecting Group for the Hydroxy Function
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Recent Developments in the Synthesis and Applications of 1,2,5-Thia- and Selenadiazoles. A Review
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SNAr hexafluoroisopropoxylation of electron-rich aryl fluoride with a catalytic electrical input
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Catalytic enantioselective reductive Eschenmoser-Claisen rearrangements
inferred← citeshttps://doi.org/10.13140/rg.2.2.22947.40486openalex-snapshot
The Design and Synthesis of Novel AOX and cytochrome bc 1 complex inhibitors which act as Phytopathogenic Fungicides
inferred← citeshttps://doi.org/10.15760/etd.7857openalex-snapshot
Synthesis of Diaryl and Alkyl-Aryl Ethers via Diaryl Iodonium Reagents
inferred← citeshttps://doi.org/10.3390/catal12111413openalex-snapshot
Microwave Assisted Esterification of Aryl/Alkyl Acids Catalyzed by N-Fluorobenzenesulfonimide
inferred← citeshttps://doi.org/10.3390/catal15010065openalex-snapshot
Cobalt(II)-Catalyzed C−H Deuteriomethoxylation of Benzamides with CD3OD
inferred← citeshttps://doi.org/10.3390/molecules23092235openalex-snapshot
Esterification of Aryl/Alkyl Acids Catalysed by N-bromosuccinimide under Mild Reaction Conditions
inferred← citeshttps://doi.org/10.3390/molecules28104251openalex-snapshot
Synthesis of meta-Aminophenol Derivatives via Cu-Catalyzed [1,3]-Rearrangement—Oxa-Michael Addition Cascade Reactions
inferred← citeshttps://doi.org/10.4172/2161-0444.1000373openalex-snapshot
Heterocycles for Alzheimer Disease: 4- and 5-Substituted Benzothiophenes as Starting Scaffold in the Construction of Potential New Inhibitors of BACE 1
inferred← citeshttps://doi.org/10.6023/cjoc202506018openalex-snapshot
Study on FeCl 3 -Mediated Reaction of Aryl Boronic Esters with Electrophiles
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