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OXIDATION OF BENZYL ALCOHOLS WITH OXONE® AND SODIUM BROMIDE

https://doi.org/10.1081/scc-120005418
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What this work says

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

inferredcites →https://doi.org/10.1016/0040-4039(96)00193-1openalex-snapshot
Selective catalytic oxidation of benzylic alcohols to the corresponding carbonyl compounds with TBHP over CrS-2
inferredcites →https://doi.org/10.1016/0040-4039(96)00295-xopenalex-snapshot
Oxidation of α,β-enones and alkenes with oxone and sodium halides: A convenient laboratory preparation of chlorine and bromine
inferredcites →https://doi.org/10.1016/b0-08-044705-8/00287-9openalex-snapshot
Aldehydes: Aryl and Heteroaryl Aldehydes
inferredcites →https://doi.org/10.1016/s0040-4020(97)10299-xopenalex-snapshot
Oxidation of aldehydes with Oxone® in aqueous acetone
inferredcites →https://doi.org/10.1016/s0040-4039(00)80531-6openalex-snapshot
The oxidation of aromatic amines in the presence of “electron-rich” aromatic systems
inferredcites →https://doi.org/10.1016/s0040-4039(00)81878-xopenalex-snapshot
Transition-metal catalyzed oxidation of alcohols to aldehydes and ketones by means of Me3SiOOSiMe3
inferredcites →https://doi.org/10.1016/s0040-4039(00)85677-4openalex-snapshot
Further studies on the utility of sodium hypochlorite in organic synthesis. Selective oxidation of diols and direct conversion of aldehydes to esters
inferredcites →https://doi.org/10.1016/s0040-4039(00)97525-7openalex-snapshot
The oxidation of alcohols and ethers using calcium hypochlorite [Ca(OCl)2]
inferredcites →https://doi.org/10.1016/s0040-4039(01)82906-3openalex-snapshot
Catalyzed oxidation of alcohols and aldehydes with iodosylbenzene
inferredcites →https://doi.org/10.1016/s0040-4039(01)93801-8openalex-snapshot
Dimethyldioxirane: Mechanism of benzaldehyde oxidation
inferredcites →https://doi.org/10.1016/s0040-4039(97)00512-1openalex-snapshot
Bromination of pyrimidines using bromide and monoperoxysulfate: A competition study between cytidine, uridine and thymidine
inferredcites →https://doi.org/10.1016/s0040-4039(98)01642-6openalex-snapshot
Hydrogen peroxide oxidation of benzylic alcohols to benzaldehydes and benzoic acids under halide-free conditions
inferredcites →https://doi.org/10.1021/ja00320a055openalex-snapshot
Production of arene oxides by the caroate-acetone system (dimethyldioxirane)
inferredcites →https://doi.org/10.1021/ja00832a040openalex-snapshot
Catalysis of peroxymonosulfate reactions by ketones
inferredcites →https://doi.org/10.1021/ja01238a049openalex-snapshot
The Reduction of Aromatic Nitro Compounds with Activated Iron
inferredcites →https://doi.org/10.1021/jo00131a018openalex-snapshot
Oxone Oxidation of Selenides: A Mild and Efficient Method for the Preparation of Selenones
inferredcites →https://doi.org/10.1021/jo00244a043openalex-snapshot
Chemistry of oxaziridines. 9. Synthesis of 2-sulfonyl- and 2-sulfamyloxaziridines using potassium peroxymonosulfate (oxone)
inferredcites →https://doi.org/10.1021/jo00388a038openalex-snapshot
Fast and selective oxidation of primary alcohols to aldehydes or to carboxylic acids and of secondary alcohols to ketones mediated by oxoammonium salts under two-phase conditions
inferredcites →https://doi.org/10.1021/jo01081a019openalex-snapshot
The Oxidation of Organic Substances by Potassium Peroxymonosulfate
inferredcites →https://doi.org/10.1021/jo01298a066openalex-snapshot
Convenient and inexpensive procedure for oxidation of secondary alcohols to ketones
inferredcites →https://doi.org/10.1021/jo9817164openalex-snapshot
Bromide Ions and Methyltrioxorhenium as Cocatalysts for Hydrogen Peroxide Oxidations and Brominations
inferredcites →https://doi.org/10.1021/ol005792gopenalex-snapshot
Catalytic Synthesis of Aldehydes and Ketones under Mild Conditions Using TEMPO/Oxone
inferredcites →https://doi.org/10.1039/a607779jopenalex-snapshot
Selective catalytic oxidation of benzyl alcohols to benzaldehydes with a dinuclear manganese(iv) complex
inferredcites →https://doi.org/10.1039/c39940001807openalex-snapshot
Copper-catalysed oxidation of hydroxy compounds by tert-butyl hydroperoxide under phase-transfer conditions
inferredcites →https://doi.org/10.1039/cs9942300357openalex-snapshot
Oxidation of some organic compounds by aqueous bromine solutions
inferredcites →https://doi.org/10.1039/ct9232303392openalex-snapshot
CCCC.—The freezing-point curves of binary mixtures of some substituted acetanilides
inferredcites →https://doi.org/10.1055/s-1992-21325openalex-snapshot
Selective Oxidation of Phenyl Sulphides to Sulphoxides or Sulphones Using Oxone® and Wet Alumina
inferredcites →https://doi.org/10.1055/s-1995-5174openalex-snapshot
Oxidative Decarboxylation of α-Amino Acids with in situ Generated Dimethyl Dioxirane
inferredcites →https://doi.org/10.1055/s-1999-2703openalex-snapshot
Oxone®: A Convenient Reagent for the Oxidation of Acetals
inferredcites →https://doi.org/10.1055/s-1999-2857openalex-snapshot
Ytterbium(III) Triflate as a Recyclable Catalyst for the Selective Atom Economic Oxidation of Benzyl Alcohols to Benzaldehydes
inferredcites →https://doi.org/10.1055/s-2001-9734openalex-snapshot
Halodecarboxylation of α,β-Unsaturated Carboxylic Acids bearing Aryl and Styrenyl Group at β-Carbon with Oxone® and Sodium Halide
inferredcites →https://doi.org/10.1081/scc-100107011openalex-snapshot
HALOGENATION OF AROMATIC METHYL KETONES USING OXONE® AND SODIUM HALIDE
inferredcites →https://doi.org/10.1201/b17118openalex-snapshot
CRC Handbook of Chemistry and Physics
inferredcites →https://doi.org/10.1246/bcsj.64.1046openalex-snapshot
Oxidation of s-Alcohols with “Oxone” in Aprotic Solvents in the Presence of Wet-Aluminium Oxide
inferredcites →https://doi.org/10.1246/cl.1983.1833openalex-snapshot
BIS(p-METHOXYPHENYL)SELENOXIDE AS A COOXIDANT FOR SELENIUM DIOXIDE OXIDATION OF BENZYL ALCOHOLS
inferredcites →https://doi.org/10.1246/cl.1984.1481openalex-snapshot
Zr-CATALYZED OXIDATION OF ALCOHOLS TO ALDEHYDES IN THE PRESENCE OF tBuOOH. HIGH REACTIVITY FOR PRIMARY AND ALLYLIC HYDROXYL FUNCTIONS
inferredcites →https://doi.org/10.1246/cl.1995.871openalex-snapshot
Oxidative Esterification of Primary Alcohols by NaBrO3/NaHSO3 Reagent in Aqueous Medium
inferredcites →https://doi.org/10.5860/choice.42-5868openalex-snapshot
Comprehensive organic functional group transformations II

What points at this work

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

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Porous Heteroatom-Doped Carbons: Efficient Catalysts for Selective Oxidation of Alcohols by Activated Persulfate
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Potassium Monoperoxysulfate
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Potassium Monoperoxysulfate
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Formation of Aldehydes and Ketones by Oxidation
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Direct Synthesis of Dialkylphosphites from White Phosphorus
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Porous Heteroatom‐Doped Carbons: Efficient Catalysts for Selective Oxidation of Alcohols by Activated Persulfate
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Oxidation of Benzyl Alcohols with Oxone® and Sodium Bromide.
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A Mild and Efficient Method for the Oxidation of Benzylic Alcohols by Two‐Phase Electrolysis.
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Catalytic N ‐Bromo Succinimide Enables Achmatowicz Rearrangement with Oxone
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Redox-mediated oxidation of alcohols using Cl− /OCl− redox couple in biphasic media
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Cobalt Single Atoms Embedded in Nitrogen‐Doped Graphene for Selective Oxidation of Benzyl Alcohol by Activated Peroxymonosulfate
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Ferric nitrate in the presence of catalytic amounts of KBr or NaBr: an efficient and homoselective catalytic media for the selective oxidation of sulfides to sulfoxides
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Selective and efficient oxidation of sulfides to sulfoxides using ammonium cerium (IV) nitrate in the presence of a catalytic amount of KBr or NaBr
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Primary alkanols: oxidative homocondensation in water and cross-condensation in methanol
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Electrochemical bromination and oxidation of alkyl aromatic compounds by two-phase electrolysis
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A cellulose-supported Mn(salen)Cl complex as an efficient heterogeneous catalyst for the selective oxidation of benzylic alcohols
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Tailoring collaborative N–O functionalities of graphene oxide for enhanced selective oxidation of benzyl alcohol
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A new and highly effective method for catalytic oxidation of alcohols to the corresponding carbonyl compounds using the tris[(2-oxazolinyl)phenolato]manganese(III)/Oxone®/n-Bu4NBr oxidation system
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Oxone/iron(II) sulfate/graphite oxide as a highly effective system for oxidation of alcohols under ultrasonic irradiation
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Bromolactonization of alkenoic acids mediated by V2O5 via bromide to bromenium in situ oxidation
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One-pot oxidative bromination – Esterification of aldehydes to 2-bromoesters using cerium (IV) ammonium nitrate and lithium bromide
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Tandem oxidation-bromination of allylic alcohols with a TEMPO-Oxone-Et4NBr reactant system
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Catalytic Environmentally Friendly Protocol for Achmatowicz Rearrangement
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Reinvestigating FeBr3-Catalyzed Alcohol Oxidation with H2O2: Is a High-Valent Iron Species (HIS) or a Reactive Brominating Species (RBS) Responsible for Alcohol Oxidation?
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Selective Single-Step Oxidation of Amine to Cross-Azo Compounds with an Unhampered Primary Benzyl Alcohol Functionality
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Status of Biocatalysis in the Production of 2,5-Furandicarboxylic Acid
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Understanding of the Oxidation Behavior of Benzyl Alcohol by Peroxymonosulfate via Carbon Nanotubes Activation
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Journey Describing Applications of Oxone in Synthetic Chemistry
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Oxidation of Borneol to Camphor Using Oxone and Catalytic Sodium Chloride: A Green Experiment for the Undergraduate Organic Chemistry Laboratory
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Selective Oxidation of Alcohols with Alkali Metal Bromides as Bromide Catalysts: Experimental Study of the Reaction Mechanism
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A new and versatile one-pot strategy to synthesize alpha-bromoketones from secondary alcohols using ammonium bromide and oxone
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Favored surface-limited oxidation of cellulose with Oxone® in water
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A solvent-free catalytic protocol for the Achmatowicz rearrangement
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Visible-Light-Driven Oxidation of N-Alkylamides to Imides Using Oxone/H2O and Catalytic KBr
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Oxone/Sodium Chloride: A Simple and Efficient Catalytic System for the Oxidation of Alcohols to Symmetric Esters and Ketones
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An expeditious and efficient method for the oxidation of benzyl alcohols by homogeneous electrolysis
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An Efficient Catalytic Oxidation of p-Alkoxypenols to p-Quinones Using Tetrabutylammonium Bromide and Oxone
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Controlling pathways and kinetics in fueled chemical reaction networks
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