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Transition Metal‐Catalyzed Directing‐Group‐Assisted C−H Activation of Phenols

https://doi.org/10.1002/cssc.201901951

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

inferredcites →https://doi.org/10.1002/adsc.201400197openalex-snapshot

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inferredcites →https://doi.org/10.1002/ange.201301451openalex-snapshot

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inferredcites →https://doi.org/10.1002/ange.201410375openalex-snapshot

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inferredcites →https://doi.org/10.1002/ange.201601999openalex-snapshot

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A Highly Para‐Selective Copper(II)‐Catalyzed Direct Arylation of Aniline and Phenol Derivatives

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CH Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals

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Cobalt‐Catalyzed Direct Arylation and Benzylation by CH/CO Cleavage with Sulfamates, Carbamates, and Phosphates

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Beyond Directing Groups: Transition‐Metal‐Catalyzed CH Activation of Simple Arenes

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Catalytic Functionalization of C(sp 2 )H and C(sp 3 )H Bonds by Using Bidentate Directing Groups

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General Method for the Synthesis of Salicylic Acids from Phenols through Palladium‐Catalyzed Silanol‐Directed CH Carboxylation

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Palladium‐Catalyzed Directed para C−H Functionalization of Phenols

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(C6F5)3B Catalyzed Chemoselective and ortho‐Selective Substitution of Phenols with α‐Aryl α‐Diazoesters

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inferredcites →https://doi.org/10.1002/asia.201601413openalex-snapshot

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Selective Hydrogenation of Phenol

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inferredcites →https://doi.org/10.1021/jo030157kopenalex-snapshot

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inferredcites →https://doi.org/10.1021/jo4011188openalex-snapshot

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inferredcites →https://doi.org/10.1021/ol201140qopenalex-snapshot

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inferredcites →https://doi.org/10.1021/ol403699dopenalex-snapshot

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Halide-free ethylation of phenol by multifunctional catalysis using phosphinite ligands

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inferredcites →https://doi.org/10.1039/c7sc04768aopenalex-snapshot

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inferredcites →https://doi.org/10.1039/c8sc02529kopenalex-snapshot

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inferredcites →https://doi.org/10.1055/s-0030-1259332openalex-snapshot

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inferredcites →https://doi.org/10.1055/s-2008-1042907openalex-snapshot

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inferredcites →https://doi.org/10.1093/ajcn/79.5.727openalex-snapshot

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inferredcites →https://doi.org/10.1111/j.1753-4887.1998.tb01670.xopenalex-snapshot

Polyphenols: Chemistry, Dietary Sources, Metabolism, and Nutritional Significance

inferredcites →https://doi.org/10.1126/science.1207661openalex-snapshot

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inferredcites →https://doi.org/10.1146/annurev.nutr.22.111401.144957openalex-snapshot

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inferredcites →https://doi.org/10.4161/oxim.2.5.9498openalex-snapshot

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inferredcites →https://doi.org/10.6023/cjoc201707031openalex-snapshot

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inferred← citeshttps://doi.org/10.1021/acs.joc.9b03322openalex-snapshot

Protecting Group-Controlled Remote Regioselective Electrophilic Aromatic Halogenation Reactions

inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02012openalex-snapshot

Copper-Mediated Regioselective C–H Sulfenylation and Selenation of Phenols with Phenanthroline Bidentate Auxiliary

inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03147openalex-snapshot

Silver-Catalyzed para-Selective Amination and Aminative Dearomatization of Phenols with Azodicarboxylates in Water

inferred← citeshttps://doi.org/10.1021/acs.orglett.1c02460openalex-snapshot

Palladium-Catalyzed Distal m-C–H Functionalization of Arylacetic Acid Derivatives

inferred← citeshttps://doi.org/10.1021/acscentsci.2c00004openalex-snapshot

Overcoming O–H Insertion to Para-Selective C–H Functionalization of Free Phenols: Rh(II)/Xantphos Catalyzed Geminal Difunctionalization of Diazo Compounds

inferred← citeshttps://doi.org/10.1039/c9ob01994dopenalex-snapshot

Recent advances in cobalt-catalysed C–H functionalizations

inferred← citeshttps://doi.org/10.1039/d0cc02889dopenalex-snapshot

Ruthenium-catalyzed regio- and site-selective ortho C–H borylation of phenol derivatives

inferred← citeshttps://doi.org/10.1039/d0ob00737dopenalex-snapshot

Lewis acid-promoted site-selective cyanation of phenols

inferred← citeshttps://doi.org/10.1039/d1qo00140jopenalex-snapshot

A simple removable aliphatic nitrile template 2-cyano-2,2-di-isobutyl acetic acid for remote meta -selective C–H functionalization

inferred← citeshttps://doi.org/10.1039/d2sc06206bopenalex-snapshot

Distal meta -C–H functionalization of α-substituted cinnamates

inferred← citeshttps://doi.org/10.1039/d3cc00289fopenalex-snapshot

Palladium-catalyzed remote meta -C–H olefination of cinnamates

inferred← citeshttps://doi.org/10.1246/cl.210439openalex-snapshot

Copper-mediated Regioselective C–H Cyanation of Phenols with Assistance of Bipyridine-type Bidentate Auxiliary

inferred← citeshttps://doi.org/10.2174/1385272827666230301144654openalex-snapshot

Cationic Ruthenium for C-H Activation Reactions

inferred← citeshttps://doi.org/10.26434/chemrxiv.13187744openalex-snapshot

Development of a Simple Removable Aliphatic Template for Remote Meta-Selective C−H Functionalization: Experimental and Computational Studies

inferred← citeshttps://doi.org/10.26434/chemrxiv.13187744.v1openalex-snapshot

Development of a Simple Removable Aliphatic Template for Remote Meta-Selective C−H Functionalization: Experimental and Computational Studies

inferred← citeshttps://doi.org/10.3390/molecules26195763openalex-snapshot

Regioselective C-H Functionalization of the Six-Membered Ring of the 6,5-Fused Heterocyclic Systems: An Overview

inferred← citeshttps://doi.org/10.3390/molecules28083397openalex-snapshot

Recent Advances in Regioselective C–H Bond Functionalization of Free Phenols

inferred← citeshttps://doi.org/10.3762/bjoc.18.100openalex-snapshot

Automated grindstone chemistry: a simple and facile way for PEG-assisted stoichiometry-controlled halogenation of phenols and anilines using N -halosuccinimides

inferred← citeshttps://doi.org/10.6023/cjoc202106011openalex-snapshot

Site-Selective C—H Iodination of Phenol Derivatives Using Aryl Iodide as Iodinating Reagent

inferred← citeshttps://doi.org/10.70675/8b66a4abz9625z4b59z9bafze696008052b0openalex-snapshot

Synthèse et applications de complexes de nickel(II) pour l’optimisation et la compréhension des réactions d’hydrofonctionnalisation et d’activation C–H.

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