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The Chemistry of Phenols

https://doi.org/10.1002/0470857277
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inferred← citeshttps://doi.org/10.2139/ssrn.4669910openalex-extracted
inferred← citeshttps://doi.org/10.1002/14356007.a08_025openalex-snapshot
Cresols and Xylenols
inferred← citeshttps://doi.org/10.1002/14356007.a19_299.pub2openalex-snapshot
Phenol
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0604openalex-snapshot
Coordination Chemistry of Metal Phenolates—General Aspects
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0605openalex-snapshot
Acid–Base and Solvation Properties of Metal Phenolates
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0619openalex-snapshot
Mass Spectrometry and Gas‐phase Ion Chemistry of Metal–phenolate and Metal–phenol complexes
inferred← citeshttps://doi.org/10.1002/9781118754887.ch14openalex-snapshot
Selective Oxidation of Aromatic Rings
inferred← citeshttps://doi.org/10.1002/9781118839621.ch5openalex-snapshot
Application of Sterically Demanding Phosphine Ligands in Palladium‐Catalyzed Cross‐Coupling leading to C( sp 2 )─E Bond Formation (E = NH 2 , OH , and F)
inferred← citeshttps://doi.org/10.1002/9781119567646.ch9openalex-snapshot
Transition‐Metal‐Catalyzed Dearomative Spiroannulation Reactions
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0112openalex-snapshot
Transition Metal‐Catalyzed Site‐Selective CH Bond Arylation of Arenes/Heteroarenes Using Quinone Diazides
inferred← citeshttps://doi.org/10.1002/admi.201500301openalex-snapshot
Lithium‐Assisted Proton Conduction at 150 °C in a Microporous Triazine‐Phenol Polymer
inferred← citeshttps://doi.org/10.1002/adsc.201201099openalex-snapshot
An Asymmetric Organocatalytic Quadruple Cascade Initiated by a Friedel–Crafts‐Type Reaction with Electron‐Rich Arenes
inferred← citeshttps://doi.org/10.1002/adsc.201300088openalex-snapshot
Pd2dba3/Bippyphos: A Robust Catalyst System for the Hydroxylation of Aryl Halides with Broad Substrate Scope
inferred← citeshttps://doi.org/10.1002/adsc.201300999openalex-snapshot
A General Approach towards Catechol and Pyrogallol through Ruthenium‐ and Palladium‐Catalyzed CH Hydroxylation by Weak Coordination
inferred← citeshttps://doi.org/10.1002/adsc.201600700openalex-snapshot
Iron‐Catalyzed Direct Alkylamination of Phenols with O‐Benzoyl‐N‐alkylhydroxylamines under Mild Conditions
inferred← citeshttps://doi.org/10.1002/adsc.201600930openalex-snapshot
Iodine‐Catalyzed Oxidative Aromatization: A Metal‐Free Concise Approach to meta‐Substituted Phenols from Cyclohex‐2‐enones
inferred← citeshttps://doi.org/10.1002/adsc.201700726openalex-snapshot
Rhodium‐Catalyzed Synthesis of Multiaryl‐substituted Naphthols via a Removable Directing Group
inferred← citeshttps://doi.org/10.1002/adsc.201801276openalex-snapshot
Phthalocyanine Zinc‐catalyzed Hydroxylation of Aryl Boronic Acids under Visible Light
inferred← citeshttps://doi.org/10.1002/adsc.201900596openalex-snapshot
Rhodium‐Catalyzed ortho‐Arylation of (Hetero)aromatic Acids
inferred← citeshttps://doi.org/10.1002/adsc.201900839openalex-snapshot
Iron‐Catalyzed Room Temperature Cross‐Couplings of Bromophenols with Aryl Grignard Reagents
inferred← citeshttps://doi.org/10.1002/adsc.202000762openalex-snapshot
Recent Advancements on Transition‐Metal‐Catalyzed, Chelation‐Induced ortho‐Hydroxylation of Arenes
inferred← citeshttps://doi.org/10.1002/adsc.202001456openalex-snapshot
Synthesis of Polysubstituted Phenols by Rhodium‐Catalyzed C−H/Diazo Coupling and Tandem Annulation
inferred← citeshttps://doi.org/10.1002/adsc.202100181openalex-snapshot
Triflic Acid‐Catalyzed Chemo‐ and Site‐Selective C−H Bond Functionalization of Phenols With 1,3‐Dienes
inferred← citeshttps://doi.org/10.1002/adsc.202300005openalex-snapshot
Metal‐free Dehydrogenation of Substituted Cyclohexanones to Phenols
inferred← citeshttps://doi.org/10.1002/adsc.202400486openalex-snapshot
Palladium‐Catalyzed Sc(OTf)3/Cs2CO3‐Assisted C−O Cross‐Coupling of Vinylidenecyclopropane‐Diesters with Phenolic Compounds
inferred← citeshttps://doi.org/10.1002/ajoc.201300192openalex-snapshot
Rapid, Sustainable, and Gram‐Scale Synthesis of Phenols Catalyzed by a Biodegradable Deep Eutectic Mixture in Water
inferred← citeshttps://doi.org/10.1002/ajoc.201500001openalex-snapshot
Synthesis of Functionalized Phenols via the Cascade Reactions of Allenic Ketones with β‐Diketones
inferred← citeshttps://doi.org/10.1002/ajoc.201500105openalex-snapshot
Reusable and Removable Directing Groups for C(sp2)−H Bond Functionalization of Arenes
inferred← citeshttps://doi.org/10.1002/ajoc.201700663openalex-snapshot
Palladium‐Catalyzed Direct Oxidative Esterification of Indoles at the C3 Position: A Novel Prospect for C(sp2)−H Acyloxylation
inferred← citeshttps://doi.org/10.1002/ange.200804898openalex-snapshot
Practical Imidazole‐Based Phosphine Ligands for Selective Palladium‐Catalyzed Hydroxylation of Aryl Halides
inferred← citeshttps://doi.org/10.1002/ange.200903639openalex-snapshot
A Very Simple Copper‐Catalyzed Synthesis of Phenols Employing Hydroxide Salts
inferred← citeshttps://doi.org/10.1002/ange.201104653openalex-snapshot
Convenient and General Palladium‐Catalyzed Carbonylative Sonogashira Coupling of Aryl Amines
inferred← citeshttps://doi.org/10.1002/ange.201207458openalex-snapshot
Pd‐Catalyzed CH Oxygenation with TFA/TFAA: Expedient Access to Oxygen‐Containing Heterocycles and Late‐Stage Drug Modification
inferred← citeshttps://doi.org/10.1002/ange.201210023openalex-snapshot
Iron‐Catalyzed Oxidative Radical Cross‐Coupling/Cyclization between Phenols and Olefins
inferred← citeshttps://doi.org/10.1002/ange.201300957openalex-snapshot
PdCl2 and N‐Hydroxyphthalimide Co‐catalyzed CH Hydroxylation by Dioxygen Activation
inferred← citeshttps://doi.org/10.1002/ange.201310572openalex-snapshot
Continuous‐Flow Synthesis of Functionalized Phenols by Aerobic Oxidation of Grignard Reagents
inferred← citeshttps://doi.org/10.1002/ange.201511007openalex-snapshot
Organo‐Iodine(III)‐Catalyzed Oxidative Phenol–Arene and Phenol–Phenol Cross‐Coupling Reaction
inferred← citeshttps://doi.org/10.1002/ange.201608013openalex-snapshot
Efficient Coupling Reaction of Quinone Monoacetal with Phenols Leading to Phenol Biaryls
inferred← citeshttps://doi.org/10.1002/ange.201608918openalex-snapshot
An Arylation Strategy to Propargylamines: Catalytic Asymmetric Friedel–Crafts‐type Arylation Reactions of C‐Alkynyl Imines
inferred← citeshttps://doi.org/10.1002/ange.201700244openalex-snapshot
Synthesis of Complex Phenols Enabled by a Rationally Designed Hydroxide Surrogate
inferred← citeshttps://doi.org/10.1002/ange.201710698openalex-snapshot
Synthesis of Phenols: Organophotoredox/Nickel Dual Catalytic Hydroxylation of Aryl Halides with Water
inferred← citeshttps://doi.org/10.1002/ange.202106440openalex-snapshot
Catalytic SNAr Hydroxylation and Alkoxylation of Aryl Fluorides
inferred← citeshttps://doi.org/10.1002/ange.202219107openalex-snapshot
Machine‐Learning Classification for the Prediction of Catalytic Activity of Organic Photosensitizers in the Nickel(II)‐Salt‐Induced Synthesis of Phenols
inferred← citeshttps://doi.org/10.1002/ange.202307251openalex-snapshot
[2+2+1+1] Cycloaddition for de novo Synthesis of Densely Functionalized Phenols
inferred← citeshttps://doi.org/10.1002/ange.202411295openalex-snapshot
Rapid Aminations of Functionalized Aryl Fluorosulfates in Water
inferred← citeshttps://doi.org/10.1002/ange.202412062openalex-snapshot
Thermally‐Stable Single‐Site Pd on CeO2 Catalyst for Selective Amination of Phenols to Aromatic Amines without External Hydrogen
inferred← citeshttps://doi.org/10.1002/ange.202412552openalex-snapshot
6‐Hydroxy Picolinohydrazides Promoted Cu(I)‐Catalyzed Hydroxylation Reaction in Water: Machine‐Learning Accelerated Ligands Design and Reaction Optimization
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.200804898openalex-snapshot
Practical Imidazole‐Based Phosphine Ligands for Selective Palladium‐Catalyzed Hydroxylation of Aryl Halides
inferred← citeshttps://doi.org/10.1002/anie.200903639openalex-snapshot
A Very Simple Copper‐Catalyzed Synthesis of Phenols Employing Hydroxide Salts
inferred← citeshttps://doi.org/10.1002/anie.201104653openalex-snapshot
Convenient and General Palladium‐Catalyzed Carbonylative Sonogashira Coupling of Aryl Amines
inferred← citeshttps://doi.org/10.1002/anie.201207458openalex-snapshot
Pd‐Catalyzed CH Oxygenation with TFA/TFAA: Expedient Access to Oxygen‐Containing Heterocycles and Late‐Stage Drug Modification
inferred← citeshttps://doi.org/10.1002/anie.201210023openalex-snapshot
Iron‐Catalyzed Oxidative Radical Cross‐Coupling/Cyclization between Phenols and Olefins
inferred← citeshttps://doi.org/10.1002/anie.201300957openalex-snapshot
PdCl2 and N‐Hydroxyphthalimide Co‐catalyzed CH Hydroxylation by Dioxygen Activation
inferred← citeshttps://doi.org/10.1002/anie.201301931openalex-snapshot
Ultrafast Solvent‐Assisted Electronic Level Crossing in 1‐Naphthol
inferred← citeshttps://doi.org/10.1002/anie.201310572openalex-snapshot
Continuous‐Flow Synthesis of Functionalized Phenols by Aerobic Oxidation of Grignard Reagents
inferred← citeshttps://doi.org/10.1002/anie.201511007openalex-snapshot
Organo‐Iodine(III)‐Catalyzed Oxidative Phenol–Arene and Phenol–Phenol Cross‐Coupling Reaction
inferred← citeshttps://doi.org/10.1002/anie.201608013openalex-snapshot
Efficient Coupling Reaction of Quinone Monoacetal with Phenols Leading to Phenol Biaryls
inferred← citeshttps://doi.org/10.1002/anie.201608918openalex-snapshot
An Arylation Strategy to Propargylamines: Catalytic Asymmetric Friedel–Crafts‐type Arylation Reactions of C‐Alkynyl Imines
inferred← citeshttps://doi.org/10.1002/anie.201700244openalex-snapshot
Synthesis of Complex Phenols Enabled by a Rationally Designed Hydroxide Surrogate
inferred← citeshttps://doi.org/10.1002/anie.201710698openalex-snapshot
Synthesis of Phenols: Organophotoredox/Nickel Dual Catalytic Hydroxylation of Aryl Halides with Water
inferred← citeshttps://doi.org/10.1002/anie.202106440openalex-snapshot
Catalytic S N Ar Hydroxylation and Alkoxylation of Aryl Fluorides
inferred← citeshttps://doi.org/10.1002/anie.202219107openalex-snapshot
Machine‐Learning Classification for the Prediction of Catalytic Activity of Organic Photosensitizers in the Nickel(II)‐Salt‐Induced Synthesis of Phenols
inferred← citeshttps://doi.org/10.1002/anie.202307251openalex-snapshot
[2+2+1+1] Cycloaddition for de novo Synthesis of Densely Functionalized Phenols
inferred← citeshttps://doi.org/10.1002/anie.202411295openalex-snapshot
Rapid Aminations of Functionalized Aryl Fluorosulfates in Water
inferred← citeshttps://doi.org/10.1002/anie.202412062openalex-snapshot
Thermally‐Stable Single‐Site Pd on CeO 2 Catalyst for Selective Amination of Phenols to Aromatic Amines without External Hydrogen
inferred← citeshttps://doi.org/10.1002/anie.202412552openalex-snapshot
6‐Hydroxy Picolinohydrazides Promoted Cu(I)‐Catalyzed Hydroxylation Reaction in Water: Machine‐Learning Accelerated Ligands Design and Reaction Optimization
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.5181openalex-snapshot
Efficient construction of C–C bonds from aryl halides/aryl esters with arylboronic acids catalysed by palladium(II) thiourea complexes
inferred← citeshttps://doi.org/10.1002/asia.201901073openalex-snapshot
Synthesis of Phenolic Compounds via Palladium Catalyzed C−H Functionalization of Arenes
inferred← citeshttps://doi.org/10.1002/bkcs.12012openalex-snapshot
Highly Porous Polycaprolactone Membrane: A Biocompatible Promotor for Oxidative Hydroxylation of Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/bkcs.12138openalex-snapshot
Choline Hydroxide as a Versatile Medium for Catalyst‐Free O‐Functionalization of Phenols
inferred← citeshttps://doi.org/10.1002/bkcs.12760openalex-snapshot
Bis(2‐pyridinyl)‐oxalamide copper complexes: Scope and limitation in CuAAC and oxidative hydroxylation of arylboronic acids
inferred← citeshttps://doi.org/10.1002/chem.200903468openalex-snapshot
A Simple and Practical Copper‐Catalyzed Approach to Substituted Phenols from Aryl Halides by Using Water as the Solvent
inferred← citeshttps://doi.org/10.1002/chem.201000470openalex-snapshot
Transition‐Metal‐Catalyzed Synthesis of Hydroxylated Arenes
inferred← citeshttps://doi.org/10.1002/chem.201002653openalex-snapshot
A General Palladium‐Catalyzed Carbonylative Sonogashira Coupling of Aryl Triflates
inferred← citeshttps://doi.org/10.1002/chem.201003711openalex-snapshot
General Copper‐Catalyzed Transformations of Functional Groups from Arylboronic Acids in Water
inferred← citeshttps://doi.org/10.1002/chem.201102683openalex-snapshot
A General Palladium‐Catalyzed Aminocarbonylation of Phenols to Primary Benzamides via In Situ Generation of Aryl Nonaflates
inferred← citeshttps://doi.org/10.1002/chem.201405071openalex-snapshot
Ruthenium(II)‐Catalyzed CH Acyloxylation of Phenols with Removable Auxiliary
inferred← citeshttps://doi.org/10.1002/chem.201503171openalex-snapshot
Microwave‐Assisted Organocatalyzed Rearrangement of Propargyl Vinyl Ethers to Salicylaldehyde Derivatives: An Experimental and Theoretical Study
inferred← citeshttps://doi.org/10.1002/chem.201701015openalex-snapshot
Asymmetric Arylative Dearomatization of β‐Naphthols Catalyzed by a Chiral Phosphoric Acid
inferred← citeshttps://doi.org/10.1002/chem.201702045openalex-snapshot
Pd‐Catalyzed Hydroxylation of Aryl Boronic Acids Using In Situ Generated Hydrogen Peroxide
inferred← citeshttps://doi.org/10.1002/chem.202003062openalex-snapshot
Insights into Ruthenium(II/IV)‐Catalyzed Distal C−H Oxygenation by Weak Coordination
inferred← citeshttps://doi.org/10.1002/chem.202005197openalex-snapshot
Developments in the Dehydrogenative Electrochemical Synthesis of 3,3′,5,5′‐Tetramethyl‐2,2′‐biphenol
inferred← citeshttps://doi.org/10.1002/chem.202102276openalex-snapshot
Turning the Light on Phenols: New Opportunities in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/clen.201800181openalex-snapshot
Removal of Phenol From Aqueous Solution Using the Green Macroalga Chara sp
inferred← citeshttps://doi.org/10.1002/cphc.200600074openalex-snapshot
Enhanced Activity and Selectivity in Cyclohexane Autoxidation by Inert H‐Bond Acceptor Catalysts
inferred← citeshttps://doi.org/10.1002/cssc.202500401openalex-snapshot
Bio‐Based Phenol from Cashew Nutshells by Catalytic Hydrocardanol Trans‐Alkylation Using H‐ZSM‐5 Zeolite
inferred← citeshttps://doi.org/10.1002/ejic.201100240openalex-snapshot
[Pd(L)Cl2]‐Catalyzed Selective Hydroxylation of Arylboronic Acids to Phenols
inferred← citeshttps://doi.org/10.1002/ejic.201300540openalex-snapshot
Copper(II) Complexes with Aromatic o‐Phosphorylated Phenols – Synthesis, Crystal Structures, and X‐ray Photoelectron Spectroscopy
inferred← citeshttps://doi.org/10.1002/ejic.201600417openalex-snapshot
Synthesis, Characterization, and Catalytic Application of Mononuclear and Dendritic Cationic CuI Iminopyridine‐Ligated Complexes in Aryl Iodide Hydroxylation
inferred← citeshttps://doi.org/10.1002/ejoc.200400811openalex-snapshot
Cobalt bis(dicarbollides)(1-) covalently attached to the calyx[4]arene platform: the first combination of organic bowl-shaped matrices and inorganic metallaborane cluster anions
inferred← citeshttps://doi.org/10.1002/ejoc.200800714openalex-snapshot
Synthesis of Isoxazolopyridobicyclooxacalix[4]arenes: A New Family of Heteracalixarene Systems
inferred← citeshttps://doi.org/10.1002/ejoc.201001180openalex-snapshot
Iron‐Catalyzed ortho‐Selective Functionalization of Phenols: A Straightforward Strategy towards the 2′‐Hydroxyphenyl‐1,2‐dione Skeleton
inferred← citeshttps://doi.org/10.1002/ejoc.201100779openalex-snapshot
Preparation of Calix[8]arene Derivatives Functionalized at a Single Methylene Bridge
inferred← citeshttps://doi.org/10.1002/ejoc.201100994openalex-snapshot
CuII–β‐Cyclodextrin Complex as a Nanocatalyst for the Homo‐ and Cross‐Coupling of Arylboronic Acids under Ligand‐ and Base‐Free Conditions in Air: Chemoselective Cross‐Coupling of Arylboronic Acids in Water
inferred← citeshttps://doi.org/10.1002/ejoc.201200368openalex-snapshot
Oxime–Palladacycle‐Catalyzed Suzuki–Miyaura Arylation and Alkenylation of Aryl Imidazolesulfonates under Aqueous and Phosphane‐Free Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.201300909openalex-snapshot
Synthesis of ortho‐Hydroxybenzophenones Catalyzed by Magnetically Retrievable Fe3O4 Nanoparticles under Ligand‐Free Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.201301228openalex-snapshot
ipso‐Hydroxylation of Arylboronic Acids and Boronate Esters by Using Sodium Chlorite as an Oxidant in Water
inferred← citeshttps://doi.org/10.1002/ejoc.201301370openalex-snapshot
Triethanolamine as an Inexpensive and Efficient Ligand for Copper‐Catalyzed Hydroxylation of Aryl Halides in Water
inferred← citeshttps://doi.org/10.1002/ejoc.201402751openalex-snapshot
Iron(III)‐Catalyzed C–H Functionalization: ortho‐Benzoyloxylation of N,N‐Dialkylanilines and Its Application to 1,4‐Benzoxazepines
inferred← citeshttps://doi.org/10.1002/ejoc.201403518openalex-snapshot
Synthesis of 2‐Acylphenol and Flavene Derivatives from the Ruthenium‐Catalyzed Oxidative C–H Acylation of Phenols with Aldehydes
inferred← citeshttps://doi.org/10.1002/ejoc.201500319openalex-snapshot
Preparation and Crystal Structure of the 1,3‐alternate Atropisomer of a Calix[4]radialene
inferred← citeshttps://doi.org/10.1002/ejoc.201501222openalex-snapshot
Enhanced Reactivity of Aerobic Diimide Olefin Hydrogenation with Arylboronic Compounds: An Efficient One‐Pot Reduction/Oxidation Protocol
inferred← citeshttps://doi.org/10.1002/ejoc.201501565openalex-snapshot
Solvent‐Dependent Regio‐ and Stereoselective Oxidation of [2.2]Paracyclophane‐Derived Phenols
inferred← citeshttps://doi.org/10.1002/ejoc.201600178openalex-snapshot
Synthesis of 4‐Quinolones: N,O‐Bis(trimethylsilyl)acetamide‐Mediated Cyclization with Cleavage of Aromatic C–O Bond
inferred← citeshttps://doi.org/10.1002/ejoc.201600508openalex-snapshot
Palladium‐Catalyzed Regioselective C–H Acetoxylation of 2‐Aryloxypyridines with 2‐Pyridyloxy as a Removable Directing Group
inferred← citeshttps://doi.org/10.1002/ejoc.201600933openalex-snapshot
ortho‐Lithiation Reactions of O‐(3,n‐Dihalophenyl) N,N‐Diethylcarbamates: Synthesis of Dihalosalicylamides and 2,3,n‐Trihalophenol Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.201700666openalex-snapshot
Oxidative Cross‐Coupling of Substituted Phenols with Unactivated Aromatics
inferred← citeshttps://doi.org/10.1002/ejoc.202301245openalex-snapshot
Ortho‐C−H Methylation and Ipso‐C−O Alkenylation of Aryl Triflates via Catellani Strategy
inferred← citeshttps://doi.org/10.1002/ejoc.202401398openalex-snapshot
Recent Advances in the Photochemical Synthesis of Esters
inferred← citeshttps://doi.org/10.1002/ejoc.70806openalex-snapshot
Copper‐Catalyzed Hydroxylation of Simple Fluoroaryl and Aryl Chlorides: A Route to (Fluoro)phenols
inferred← citeshttps://doi.org/10.1002/hc.21138openalex-snapshot
Boric Acid as Highly Efficient Catalyst for the Synthesis of Phenols from Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/hlca.202300059openalex-snapshot
Phenols as Novel Photocatalytic Platforms for Organic Synthesis
inferred← citeshttps://doi.org/10.1002/jrs.1791openalex-snapshot
Theoretical and experimental studies on the adsorption behavior of thiophenol on gold nanoparticles
inferred← citeshttps://doi.org/10.1002/poc.1394openalex-snapshot
Structural aspects of the intermolecular hydrogen bond strength: H‐bonded complexes of aniline, phenol and pyridine derivatives
inferred← citeshttps://doi.org/10.1002/poc.1696openalex-snapshot
Proton coupled electron transfer reaction of phenols with excited state ruthenium(II) – polypyridyl complexes
inferred← citeshttps://doi.org/10.1002/poc.3462openalex-snapshot
The Baeyer‐Villiger oxidation versus aromatic ring hydroxylation: competing organic peracid oxidation mechanisms explored by multivariate modelling of designed multi‐response experiments
inferred← citeshttps://doi.org/10.1002/poc.3538openalex-snapshot
Experimental (FT‐IR) and theoretical (DFT) studies on prototropy and H‐bond formation for pyrazine‐2‐amidoxime
inferred← citeshttps://doi.org/10.1002/rem.21663openalex-snapshot
Removal of substituted phenols onto iron‐treated Nostoc sp. biomass
inferred← citeshttps://doi.org/10.1002/slct.201600170openalex-snapshot
One‐Step Synthesis of Xanthones and Thio‐Xanthones by Using Magnetically Separable Copper ferrite Nanoparticles as a Catalyst under Ligand Free Conditions
inferred← citeshttps://doi.org/10.1002/slct.201601606openalex-snapshot
Aerobic Water–based Oxidation of 2,3,6‐Trimethylphenol to Trimethyl‐1,4‐benzoquinone over Copper(II) Nitrate Catalyst
inferred← citeshttps://doi.org/10.1002/slct.201703036openalex-snapshot
Ascorbic Acid as a Highly Efficient Organocatalyst for ipso ‐Hydroxylation of Arylboronic Acid
inferred← citeshttps://doi.org/10.1002/slct.201803521openalex-snapshot
L‐Proline‐Catalyzed One‐Pot Diastereoselective Synthesis of Cyclohexanols from β‐Aryl‐γ‐nitroketones and α,β‐Unsaturated Aldehydes: A New Route to 2,3,4,6‐Tetrasubstituted Phenols
inferred← citeshttps://doi.org/10.1002/slct.201901170openalex-snapshot
Cu‐Mediated C7 Acetoxylation of Indolines
inferred← citeshttps://doi.org/10.1002/slct.201902860openalex-snapshot
Copper‐Mediated Decarboxylative C–H Arylation of Phenol Derivatives with ortho ‐Nitrobenzoic Acids Using Phenanthroline‐Based Bidentate Auxiliary
inferred← citeshttps://doi.org/10.1002/slct.202101723openalex-snapshot
Interplay of Hydrogen and Halogen Bonding in the Crystal Structures of 2,6‐Dihalogenated Phenols
inferred← citeshttps://doi.org/10.1002/tcr.202300020openalex-snapshot
Recent Advances in Carbon‐Nitrogen/Carbon‐Oxygen Bond Formation Under Transition‐Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1007/3418_2012_42openalex-snapshot
Catalytic Transformations Involving the Activation of sp2 Carbon–Oxygen Bonds
inferred← citeshttps://doi.org/10.1007/978-1-4614-9329-7_17openalex-snapshot
Catalytic Oxidation of Lignin for the Production of Low Molecular Weight Aromatics
inferred← citeshttps://doi.org/10.1007/978-3-319-49784-6_5openalex-snapshot
Nickel-Catalyzed Cross-Coupling Reactions of Unreactive Phenolic Electrophiles via C–O Bond Activation
inferred← citeshttps://doi.org/10.1007/978-3-540-88417-0_2openalex-snapshot
Synthesis (Manufacture, Production) of Plastics
inferred← citeshttps://doi.org/10.1007/978-3-642-45149-2_6openalex-snapshot
Chemical Bonding and Aromaticity in Poly-heterocyclic Compounds
inferred← citeshttps://doi.org/10.1007/978-94-017-0448-9_25openalex-snapshot
Hydrogen Bonding and the Energetics of Homolytic Dissociation in Solution
inferred← citeshttps://doi.org/10.1007/s00253-018-9328-3openalex-snapshot
A hydroquinone-specific screening system for directed P450 evolution
inferred← citeshttps://doi.org/10.1007/s10311-005-0112-0openalex-snapshot
Phototransformation of fibrate drugs in aqueous media
inferred← citeshttps://doi.org/10.1007/s10311-021-01253-4openalex-snapshot
Ashes from organic waste as reagents in synthetic chemistry: a review
inferred← citeshttps://doi.org/10.1007/s10498-009-9077-0openalex-snapshot
Reduction of Substituted p-Benzoquinones by FeII Near Neutral pH
inferred← citeshttps://doi.org/10.1007/s10562-019-02682-1openalex-snapshot
Heterogeneous Palladium–Chitosan–CNT Core–Shell Nanohybrid Composite for Ipso-hydroxylation of Arylboronic Acids
inferred← citeshttps://doi.org/10.1007/s10562-022-04148-3openalex-snapshot
Preparation of Copper Catalysts Immobilized on Poly(3-carboxypropyl)Thiophene and Their Application in Organic Transformation
inferred← citeshttps://doi.org/10.1007/s10812-026-02064-7openalex-snapshot
Transformation of Phenol in Solid Mixtures with Humic Acids During Electron Beam Irradiation
inferred← citeshttps://doi.org/10.1007/s10847-018-0800-6openalex-snapshot
Preparation, characterization of new Co(II) and Cu(II) phthalocyanines and their catalytic performances in aerobic oxidation of substituted phenols
inferred← citeshttps://doi.org/10.1007/s10973-009-0647-6openalex-snapshot
Thermochemistry of hydroxymethylphenol isomers
inferred← citeshttps://doi.org/10.1007/s11090-016-9725-2openalex-snapshot
Kinetics and Mechanism of Cr(VI) Reduction in a Water Cathode Induced by Atmospheric Pressure DC Discharge in Air
inferred← citeshttps://doi.org/10.1007/s11094-014-1032-8openalex-snapshot
Synthesis, Toxicity, and Antituberculosis Activity of Isoniazid Derivatives Containing Sterically Hindered Phenols
inferred← citeshttps://doi.org/10.1007/s11144-016-1097-3openalex-snapshot
Photocatalytic degradation of phenol using doped titania supported on photonic SiO2 spheres
inferred← citeshttps://doi.org/10.1007/s11172-011-0144-5openalex-snapshot
Reactions of pyrazinium salts with phenols:from σH-adducts to SN Hproducts and transformations into benzo[b]furans
inferred← citeshttps://doi.org/10.1007/s11224-005-6980-xopenalex-snapshot
Interplay of Thermochemistry and Structural Chemistry, the Journal (Volume 14, 2003) and the Discipline
inferred← citeshttps://doi.org/10.1007/s11224-006-9038-9openalex-snapshot
Interplay of thermochemistry and structural chemistry, the journal (volume 15, 2004) and the discipline
inferred← citeshttps://doi.org/10.1007/s11224-009-9474-4openalex-snapshot
Interplay of thermochemistry and Structural Chemistry, the journal (volume 19, 2008) and the discipline
inferred← citeshttps://doi.org/10.1007/s11224-009-9506-0openalex-snapshot
Interplay of thermochemistry and Structural Chemistry, the journal (volume 17, 2006) and the discipline
inferred← citeshttps://doi.org/10.1007/s11224-010-9656-0openalex-snapshot
Interplay of thermochemistry and Structural Chemistry, the journal (volume 20, 2009) and the discipline
inferred← citeshttps://doi.org/10.1007/s11224-011-9769-0openalex-snapshot
Interplay of thermochemistry and Structural Chemistry, the journal (volume 21, 2010) and the discipline
inferred← citeshttps://doi.org/10.1007/s11224-012-0018-yopenalex-snapshot
Structure-based evaluation of the regioselectivity in bifurcated hydrogen bonds
inferred← citeshttps://doi.org/10.1007/s11224-014-0484-5openalex-snapshot
A theoretical study of the thermodynamic and hydrogen-bond basicity of TEMPO radical and related nitroxides
inferred← citeshttps://doi.org/10.1007/s11224-017-0965-4openalex-snapshot
How OH and O– groups affect electronic structure of meta-substituted and para-substituted phenols and phenolates
inferred← citeshttps://doi.org/10.1007/s11224-017-1066-0openalex-snapshot
Reactivity indexes of antioxidant molecules from Rosmarinus officinalis
inferred← citeshttps://doi.org/10.1007/s11224-019-01360-7openalex-snapshot
On the relations between aromaticity and substituent effect
inferred← citeshttps://doi.org/10.1007/s11270-014-2143-2openalex-snapshot
Structural Influence on Photooxidative Degradation of Halogenated Phenols
inferred← citeshttps://doi.org/10.1007/s11426-014-5138-3openalex-snapshot
Highly efficient nickel/phosphine catalyzed cross-couplings of diarylborinic acids with aryl tosylates and sulfamates
inferred← citeshttps://doi.org/10.1007/s11426-015-5382-1openalex-snapshot
Palladium-catalyzed R2(O)P-directed C(sp2)-H activation
inferred← citeshttps://doi.org/10.1007/s11434-014-0239-0openalex-snapshot
Progress of transition metal-catalyzed cross-coupling mediated by PyBroP
inferred← citeshttps://doi.org/10.1007/s11783-017-0970-2openalex-snapshot
Phenolic compounds removal by wet air oxidation based processes
inferred← citeshttps://doi.org/10.1007/s12039-024-02333-yopenalex-snapshot
Utilization of Fe3O4@MgO as a heterogeneous solid-base in functional group transformations of arylboronic acids, phenols and benzonitriles
inferred← citeshttps://doi.org/10.1007/s13738-014-0528-1openalex-snapshot
Photoluminescence electron transfer quenching of ruthenium(II)-polypyridyl complexes with biologically important phenolate ions in aqueous acetonitrile solution
inferred← citeshttps://doi.org/10.1007/s13738-019-01707-1openalex-snapshot
Versatile catalysis of “natural extract”: oxidation of sulfides and alcohols and ipso-hydroxylation of arylboronic acids
inferred← citeshttps://doi.org/10.1007/s13762-019-02272-zopenalex-snapshot
Direct sunlight-driven degradation of 2-chlorophenol catalyzed by kaolinite-supported ZnO
inferred← citeshttps://doi.org/10.1007/s40071-014-0062-xopenalex-snapshot
Comparative studies on properties and antioxidative activity of fish skin gelatin films incorporated with essential oils from various sources
inferred← citeshttps://doi.org/10.1007/s41745-019-00158-0openalex-snapshot
Hydrogen Bonding Effects on Vibrational Dynamics and Photochemistry in Selected Binary Molecular Complexes
inferred← citeshttps://doi.org/10.1016/b978-0-12-818806-4.00008-5openalex-snapshot
Current heterogeneous catalytic processes for environmental remediation of air, water, and soil
inferred← citeshttps://doi.org/10.1016/bs.adomc.2016.07.001openalex-snapshot
Phenol Derivatives
inferred← citeshttps://doi.org/10.1016/j.aca.2018.08.007openalex-snapshot
Experimental development of a biosensor system to measure the concentration of phenol diluted in water using alternative sources of oxidoreductase enzymes
inferred← citeshttps://doi.org/10.1016/j.apcata.2008.01.031openalex-snapshot
Oxidation of 2,3,6-trimethylphenol with potassium peroxymonosulfate catalyzed by iron and cobalt phthalocyanine tetrasulfonates in a methanol–water mixture
inferred← citeshttps://doi.org/10.1016/j.apcata.2013.06.051openalex-snapshot
Clay entrapped Cu(OH) as an efficient heterogeneous catalyst for ipso-hydroxylation of arylboronic acids
inferred← citeshttps://doi.org/10.1016/j.apcata.2015.09.036openalex-snapshot
Effect of the irradiation wavelength on the performance of nanoporous carbon as an additive to TiO2
inferred← citeshttps://doi.org/10.1016/j.apcatb.2016.08.037openalex-snapshot
Electrochemical advanced oxidation processes: A review on their application to synthetic and real wastewaters
inferred← citeshttps://doi.org/10.1016/j.asoc.2009.10.018openalex-snapshot
Model-free control based on reinforcement learning for a wastewater treatment problem
inferred← citeshttps://doi.org/10.1016/j.bcp.2008.04.003openalex-snapshot
Ubiquinone and tocopherol: Dissimilar siblings
inferred← citeshttps://doi.org/10.1016/j.biombioe.2014.03.065openalex-snapshot
Conversion of cacao pod husks by pyrolysis and catalytic reaction to produce useful chemicals
inferred← citeshttps://doi.org/10.1016/j.biortech.2005.06.017openalex-snapshot
Impact of reaction conditions on the laccase-catalyzed conversion of bisphenol A
inferred← citeshttps://doi.org/10.1016/j.biortech.2007.08.072openalex-snapshot
Biocatalytic oxidation of bisphenol A in a reverse micelle system using horseradish peroxidase
inferred← citeshttps://doi.org/10.1016/j.bmc.2013.06.050openalex-snapshot
Tocopheramines and tocotrienamines as antioxidants: ESR spectroscopy, rapid kinetics and DFT calculations
inferred← citeshttps://doi.org/10.1016/j.catcom.2019.02.017openalex-snapshot
Selective activation of C H bond into C O bond of phenols in para-position via aerobic oxidation
inferred← citeshttps://doi.org/10.1016/j.catcom.2020.106277openalex-snapshot
Selective activation of C H bond of phenol in ortho-position into C OH bond in a two-phase system
inferred← citeshttps://doi.org/10.1016/j.cclet.2014.03.018openalex-snapshot
Metal-free synthesis of substituted phenols from arylboronic acids in water at room temperature
inferred← citeshttps://doi.org/10.1016/j.ccr.2015.07.019openalex-snapshot
Recent advances in transition-metal-catalyzed selective oxidation of substituted phenols and methoxyarenes with environmentally benign oxidants
inferred← citeshttps://doi.org/10.1016/j.ccr.2018.11.001openalex-snapshot
Building molecular complexity through transition-metal-catalyzed oxidative annulations/cyclizations: Harnessing the utility of phenols, naphthols and 1,3-dicarbonyl compounds
inferred← citeshttps://doi.org/10.1016/j.cej.2008.11.036openalex-snapshot
Adsorption of phenolic compounds on some hybrid xerogels
inferred← citeshttps://doi.org/10.1016/j.cej.2015.04.082openalex-snapshot
Prediction of key structural features responsible for aromaticity of single-benzene ring pollutants and their photooxidative intermediates
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.132763openalex-snapshot
Prediction of reaction mechanism for OH radical-mediated phenol oxidation using quantum chemical calculation
inferred← citeshttps://doi.org/10.1016/j.chemphys.2004.06.041openalex-snapshot
Electronic spectroscopy of 1-naphthol/solvent clusters 1-NpOH/S, S = H2O, Ar and N2
inferred← citeshttps://doi.org/10.1016/j.chemphys.2009.12.004openalex-snapshot
Direct and ketone-sensitized photoconversion of 1-nitro-9,10-anthraquinone to 1-amino-9,10-anthraquinone mediated by donor radicals
inferred← citeshttps://doi.org/10.1016/j.chemphyslip.2009.10.005openalex-snapshot
Oxidizability of cardiac cardiolipin in Triton X-100 micelles as determined by using a Clark electrode
inferred← citeshttps://doi.org/10.1016/j.cis.2020.102267openalex-snapshot
Applications of tannic acid in membrane technologies: A review
inferred← citeshttps://doi.org/10.1016/j.clay.2021.106098openalex-snapshot
Rational design of kaolinite-based photocatalytic materials for environment decontamination
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2017.10.019openalex-snapshot
Development of a graphene oxide/chitosan nanocomposite for the removal of picric acid from aqueous solutions: Study of sorption parameters
inferred← citeshttps://doi.org/10.1016/j.comptc.2010.10.022openalex-snapshot
Tautomeric preferences and π-electron delocalization for redox forms of phenol
inferred← citeshttps://doi.org/10.1016/j.crgsc.2021.100107openalex-snapshot
Deep eutectic solvent mediated controlled and selective oxidation of organic sulfides and hydroxylation of arylboronic acids
inferred← citeshttps://doi.org/10.1016/j.electacta.2010.07.096openalex-snapshot
Infrared and UV–vis spectra of phenoxonium cations produced during the oxidation of phenols with structures similar to vitamin E
inferred← citeshttps://doi.org/10.1016/j.fct.2010.01.006openalex-snapshot
Concentration dependent effects of commonly used pesticides on activation versus inhibition of the quince (Cydonia Oblonga) polyphenol oxidase
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