Research graph
References from [ <scp>OH</scp> ‐ <scp>TEMPO</scp> ] <sup>+</sup> [ <scp> NO <sub>3</sub> </scp> ] <sup>–</sup> : A Metal‐Free and Cost‐Effective Catalyst for Aerobic Oxidation of Alcohols. Local targets link to admitted publications; unresolved targets remain external evidence.
Hydrogen‐Bonding‐Driven Site‐Selective Activation of α‐C(sp3)–H in Alcohols: A Straightforward Dual‐Catalysis Strategy for Efficient Acceptorless Dehydrogenation
10.1002/anie.202506022 · 2025 · External reference
Large scale oxidations in the pharmaceutical industry
10.1021/cr040679f · 2006 · External reference
Oxidation of Alcohols with Molecular Oxygen on Solid Catalysts
10.1021/cr0200116 · 2004 · External reference
Recent advances on oxidation of alcohols over various types of materials as effective catalysts: An overview
10.1016/j.ccr.2024.216372 · 2025 · External reference
Catalytic Oxidation of Alcohols
10.1016/bs.adomc.2015.02.004 · 2015 · External reference
Ligand‐Modulated Palladium‐Catalyzed Aerobic Alcohol Oxidations
10.1021/ar040243m · 2006 · External reference
Green, Catalytic Oxidations of Alcohols
10.1021/ar010075n · 2002 · External reference
Optimizing the Synthetic Potential of O2: Implications of Overpotential in Homogeneous Aerobic Oxidation Catalysis
10.1021/jacs.3c02887 · 2023 · External reference
A comprehensive and updated review of studies on the oxidation of cyclohexane to produce ketone‐alcohol (KA) oil
10.1515/revce-2020-0059 · 2022 · External reference
Chemoselective Aerobic Oxidation of Alcohols Utilizing a Vanadium(V) Catalyst
10.1021/acscatal.3c05638 · 2024 · External reference
Catalytic oxidation of alcohols to aldehydes and ketones with ferric nitrate nonahydrate/trifluoroacetic acid via mechanochemical reaction
10.1016/j.tetlet.2024.155079 · 2024 · External reference
Efficient Aerobic Oxidation of Secondary Alcohols at Ambient Temperature with an ABNO/NOx Catalyst System
10.1021/cs400746m · 2013 · External reference
Oxoammonium and Nitroxide‐Catalyzed Oxidations of Alcohols
2009 · External reference
CO2‐Catalyzed Oxidation of Benzylic and Allylic Alcohols with DMSO
10.1021/acscatal.7b04390 · 2018 · External reference
A Revised Preparation of (4‐Acetamido‐2,2,6,6‐tetramethylpiperidin‐1‐yl)oxyl and 4‐Acetamido‐2,2,6,6‐tetramethyl‐1‐oxopiperidinium Tetrafluoroborate: Reagents for Stoichiometric Oxidations of Alcohols
10.1055/s-0032-1317861 · 2012 · External reference
Synthesis of 4‐acetamido‐2,2,6,6‐tetramethylpiperidine‐1‐oxoammonium tetrafluoroborate and 4‐acetamido‐(2,2,6,6‐tetramethyl‐piperidin‐1‐yl)oxyl and their use in oxidative reactions
10.1038/nprot.2013.028 · 2013 · External reference
Oxoammonium Salt Oxidations of Alcohols in the Presence of Pyridine Bases
10.1021/jo402519m · 2014 · External reference
Mechanism of the Oxidation of Alcohols by Oxoammonium Cations
10.1021/jo0704614 · 2007 · External reference
Recent advancements in the use of Bobbitt's salt and 4‐acetamidoTEMPO
10.1039/d3cc04709a · 2023 · External reference
Organic Synthesis Using Nitroxides
10.1021/acs.chemrev.3c00212 · 2023 · External reference
Oxidation of Alcohols to Aldehydes and Ketones Using a Catalytic Pairing of a Nitroxide and Nitric Acid
10.1055/a-2217-9577 · 2023 · External reference
Probing the Effect of Counterions on the Oxidation of Alcohols Using Oxoammonium Salts
2020 · External reference
Silica gel‐supported TEMPO with adsorbed NO x for selective oxidation of alcohols under mild conditions
10.1016/s1872-2067(12)60657-3 · 2013 · External reference
Iodine as a Chemoselective Reoxidant of TEMPO: Application to the Oxidation of Alcohols to Aldehydes and Ketones
10.1021/ol0272444 · 2003 · External reference
A New Modified “Montanari Oxidation Process” by Means of Chlorine Dissolved in the Reaction Solvent as Oxidant and TEMPO as Catalyst: Oxidation of 3‐S‐Quinuclidinol to 3‐Quinuclidinone
10.1021/op010096x · 2002 · External reference
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
10.1021/jo00388a038 · 1987 · External reference
Iron Chloride/4‐Acetamido‐TEMPO/Sodium Nitrite‐Catalyzed Aerobic Oxidation of Primary Alcohols to the Aldehydes
10.1002/adsc.200900662 · 2010 · External reference
Iron/ABNO‐Catalyzed Aerobic Oxidation of Alcohols to Aldehydes and Ketones under Ambient Atmosphere
10.1021/acs.joc.6b00009 · 2016 · External reference
A TEMPO‐Free Copper‐Catalyzed Aerobic Oxidation of Alcohols
10.1002/anie.201411483 · 2015 · External reference
Iron(III) Nitrate/TEMPO‐Catalyzed Aerobic Alcohol Oxidation: Distinguishing between Serial versus Integrated Redox Cooperativity
10.1021/jacs.1c05224 · 2021 · External reference
Copper(II)‐ catalysed aerobic oxidation of primary alcohols to aldehydes
2003 · External reference
Catalytic Activity Dependency on Catalyst Components in Aerobic Copper‐TEMPO Oxidation
10.1002/chem.200901245 · 2009 · External reference
Transition‐Metal‐Free: A Highly Efficient Catalytic Aerobic Alcohol Oxidation Process
10.1021/ja031765k · 2004 · External reference
Efficient NO Equivalent for Activation of Molecular Oxygen and Its Applications in Transition Metal Free Catalytic Aerobic Alcohol Oxidation
10.1021/jo0705824 · 2007 · External reference
Flavin Nitroalkane Oxidase Mimics Compatibility with NO x /TEMPO Catalysis: Aerobic Oxidization of Alcohols, Diols, and Ethers
10.1021/acs.joc.0c01013 · 2020 · External reference
Selective Aerobic Oxidation of Alcohols with NO3− Activated Nitroxyl Radical/Manganese Catalyst System
10.1002/cctc.201800438 · 2018 · External reference
TEMPO/HCl/NaNO2 Catalyst: A Transition‐Metal‐Free Approach to Efficient Aerobic Oxidation of Alcohols to Aldehydes and Ketones Under Mild Conditions
10.1002/chem.200701818 · 2008 · External reference
Highly Practical Copper(I)/TEMPO Catalyst System for Chemoselective Aerobic Oxidation of Primary Alcohols
10.1021/ja206230h · 2011 · External reference
Mechanism of Copper(I)/TEMPO‐Catalyzed Aerobic Alcohol Oxidation
10.1021/ja3117203 · 2013 · External reference
Copper(I)/ABNO‐Catalyzed Aerobic Alcohol Oxidation: Alleviating Steric and Electronic Constraints of Cu/TEMPO Catalyst Systems
10.1021/ja409241h · 2013 · External reference
Development of a General and Practical Iron Nitrate/TEMPO‐Catalyzed Aerobic Oxidation of Alcohols to Aldehydes/Ketones: Catalysis with Table Salt
10.1002/adsc.201100033 · 2011 · External reference
Iron Catalysis for Room‐Temperature Aerobic Oxidation of Alcohols to Carboxylic Acids
10.1021/jacs.6b03948 · 2016 · External reference
Iron‐Catalyzed Aerobic Oxidation of Alcohols: Lower Cost and Improved Selectivity
10.1021/acs.oprd.8b00374 · 2019 · External reference
Highly Efficient, Organocatalytic Aerobic Alcohol Oxidation
10.1021/ja110940c · 2011 · External reference
Oxidation of alcohols using an oxoammonium salt bearing the nitrate anion
10.1016/j.tetlet.2019.151464 · 2020 · External reference
Fast, easy oxidation of alcohols using an oxoammonium salt bearing the nitrate anion
10.1016/j.tetlet.2022.154332 · 2023 · External reference
Oxidation of diols using a substoichiometric quantity of an oxoammonium salt bearing the nitrate anion
10.1016/j.tetlet.2024.155203 · 2024 · External reference
Toward a Unified Mechanism for Oxoammonium Salt‐Mediated Oxidation Reactions: A Theoretical and Experimental Study Using a Hydride Transfer Model
10.1021/acs.joc.5b01240 · 2015 · External reference
Practical Aerobic Oxidations of Alcohols and Amines with Homogeneous Copper/TEMPO and Related Catalyst Systems
10.1002/anie.201403110 · 2014 · External reference
The Deuterium Isotope Effect in the Side Chain Halogenation of Toluene
10.1021/ja01545a034 · 1958 · External reference
Iron Chloride/4‐Acetamido‐TEMPO/Sodium Nitrite‐Catalyzed Aerobic Oxidation of Primary Alcohols to the Aldehydes
10.1002/adsc.200900662 · ExternalCitation · doi-reference
Development of a General and Practical Iron Nitrate/TEMPO‐Catalyzed Aerobic Oxidation of Alcohols to Aldehydes/Ketones: Catalysis with Table Salt
10.1002/adsc.201100033 · ExternalCitation · doi-reference
Practical Aerobic Oxidations of Alcohols and Amines with Homogeneous Copper/TEMPO and Related Catalyst Systems
10.1002/anie.201403110 · ExternalCitation · doi-reference
A TEMPO‐Free Copper‐Catalyzed Aerobic Oxidation of Alcohols
10.1002/anie.201411483 · ExternalCitation · doi-reference
Hydrogen‐Bonding‐Driven Site‐Selective Activation of α‐C(sp3)–H in Alcohols: A Straightforward Dual‐Catalysis Strategy for Efficient Acceptorless Dehydrogenation
10.1002/anie.202506022 · ExternalCitation · doi-reference
Selective Aerobic Oxidation of Alcohols with NO3− Activated Nitroxyl Radical/Manganese Catalyst System
10.1002/cctc.201800438 · ExternalCitation · doi-reference
TEMPO/HCl/NaNO2 Catalyst: A Transition‐Metal‐Free Approach to Efficient Aerobic Oxidation of Alcohols to Aldehydes and Ketones Under Mild Conditions
10.1002/chem.200701818 · ExternalCitation · doi-reference
Catalytic Activity Dependency on Catalyst Components in Aerobic Copper‐TEMPO Oxidation
10.1002/chem.200901245 · ExternalCitation · doi-reference
Catalytic Oxidation of Alcohols
10.1016/bs.adomc.2015.02.004 · ExternalCitation · doi-reference
Recent advances on oxidation of alcohols over various types of materials as effective catalysts: An overview
10.1016/j.ccr.2024.216372 · ExternalCitation · doi-reference
Oxidation of alcohols using an oxoammonium salt bearing the nitrate anion
10.1016/j.tetlet.2019.151464 · ExternalCitation · doi-reference
Fast, easy oxidation of alcohols using an oxoammonium salt bearing the nitrate anion
10.1016/j.tetlet.2022.154332 · ExternalCitation · doi-reference
Catalytic oxidation of alcohols to aldehydes and ketones with ferric nitrate nonahydrate/trifluoroacetic acid via mechanochemical reaction
10.1016/j.tetlet.2024.155079 · ExternalCitation · doi-reference
Oxidation of diols using a substoichiometric quantity of an oxoammonium salt bearing the nitrate anion
10.1016/j.tetlet.2024.155203 · ExternalCitation · doi-reference
Silica gel‐supported TEMPO with adsorbed NO x for selective oxidation of alcohols under mild conditions
10.1016/s1872-2067(12)60657-3 · ExternalCitation · doi-reference
Organic Synthesis Using Nitroxides
10.1021/acs.chemrev.3c00212 · ExternalCitation · doi-reference
Flavin Nitroalkane Oxidase Mimics Compatibility with NO x /TEMPO Catalysis: Aerobic Oxidization of Alcohols, Diols, and Ethers
10.1021/acs.joc.0c01013 · ExternalCitation · doi-reference
Toward a Unified Mechanism for Oxoammonium Salt‐Mediated Oxidation Reactions: A Theoretical and Experimental Study Using a Hydride Transfer Model
10.1021/acs.joc.5b01240 · ExternalCitation · doi-reference
Iron/ABNO‐Catalyzed Aerobic Oxidation of Alcohols to Aldehydes and Ketones under Ambient Atmosphere
10.1021/acs.joc.6b00009 · ExternalCitation · doi-reference
Iron‐Catalyzed Aerobic Oxidation of Alcohols: Lower Cost and Improved Selectivity
10.1021/acs.oprd.8b00374 · ExternalCitation · doi-reference
Chemoselective Aerobic Oxidation of Alcohols Utilizing a Vanadium(V) Catalyst
10.1021/acscatal.3c05638 · ExternalCitation · doi-reference
CO2‐Catalyzed Oxidation of Benzylic and Allylic Alcohols with DMSO
10.1021/acscatal.7b04390 · ExternalCitation · doi-reference
Green, Catalytic Oxidations of Alcohols
10.1021/ar010075n · ExternalCitation · doi-reference
Ligand‐Modulated Palladium‐Catalyzed Aerobic Alcohol Oxidations
10.1021/ar040243m · ExternalCitation · doi-reference
Oxidation of Alcohols with Molecular Oxygen on Solid Catalysts
10.1021/cr0200116 · ExternalCitation · doi-reference
Large scale oxidations in the pharmaceutical industry
10.1021/cr040679f · ExternalCitation · doi-reference
Efficient Aerobic Oxidation of Secondary Alcohols at Ambient Temperature with an ABNO/NOx Catalyst System
10.1021/cs400746m · ExternalCitation · doi-reference
The Deuterium Isotope Effect in the Side Chain Halogenation of Toluene
10.1021/ja01545a034 · ExternalCitation · doi-reference
Transition‐Metal‐Free: A Highly Efficient Catalytic Aerobic Alcohol Oxidation Process
10.1021/ja031765k · ExternalCitation · doi-reference
Highly Efficient, Organocatalytic Aerobic Alcohol Oxidation
10.1021/ja110940c · ExternalCitation · doi-reference
Highly Practical Copper(I)/TEMPO Catalyst System for Chemoselective Aerobic Oxidation of Primary Alcohols
10.1021/ja206230h · ExternalCitation · doi-reference
Mechanism of Copper(I)/TEMPO‐Catalyzed Aerobic Alcohol Oxidation
10.1021/ja3117203 · ExternalCitation · doi-reference
Copper(I)/ABNO‐Catalyzed Aerobic Alcohol Oxidation: Alleviating Steric and Electronic Constraints of Cu/TEMPO Catalyst Systems
10.1021/ja409241h · ExternalCitation · doi-reference
Iron(III) Nitrate/TEMPO‐Catalyzed Aerobic Alcohol Oxidation: Distinguishing between Serial versus Integrated Redox Cooperativity
10.1021/jacs.1c05224 · ExternalCitation · doi-reference
Optimizing the Synthetic Potential of O2: Implications of Overpotential in Homogeneous Aerobic Oxidation Catalysis
10.1021/jacs.3c02887 · ExternalCitation · doi-reference
Iron Catalysis for Room‐Temperature Aerobic Oxidation of Alcohols to Carboxylic Acids
10.1021/jacs.6b03948 · ExternalCitation · doi-reference
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
10.1021/jo00388a038 · ExternalCitation · doi-reference
Mechanism of the Oxidation of Alcohols by Oxoammonium Cations
10.1021/jo0704614 · ExternalCitation · doi-reference
Efficient NO Equivalent for Activation of Molecular Oxygen and Its Applications in Transition Metal Free Catalytic Aerobic Alcohol Oxidation
10.1021/jo0705824 · ExternalCitation · doi-reference
Oxoammonium Salt Oxidations of Alcohols in the Presence of Pyridine Bases
10.1021/jo402519m · ExternalCitation · doi-reference
Iodine as a Chemoselective Reoxidant of TEMPO: Application to the Oxidation of Alcohols to Aldehydes and Ketones
10.1021/ol0272444 · ExternalCitation · doi-reference
A New Modified “Montanari Oxidation Process” by Means of Chlorine Dissolved in the Reaction Solvent as Oxidant and TEMPO as Catalyst: Oxidation of 3‐S‐Quinuclidinol to 3‐Quinuclidinone
10.1021/op010096x · ExternalCitation · doi-reference
Synthesis of 4‐acetamido‐2,2,6,6‐tetramethylpiperidine‐1‐oxoammonium tetrafluoroborate and 4‐acetamido‐(2,2,6,6‐tetramethyl‐piperidin‐1‐yl)oxyl and their use in oxidative reactions
10.1038/nprot.2013.028 · ExternalCitation · doi-reference
Recent advancements in the use of Bobbitt's salt and 4‐acetamidoTEMPO
10.1039/d3cc04709a · ExternalCitation · doi-reference
Oxidation of Alcohols to Aldehydes and Ketones Using a Catalytic Pairing of a Nitroxide and Nitric Acid
10.1055/a-2217-9577 · ExternalCitation · doi-reference
A Revised Preparation of (4‐Acetamido‐2,2,6,6‐tetramethylpiperidin‐1‐yl)oxyl and 4‐Acetamido‐2,2,6,6‐tetramethyl‐1‐oxopiperidinium Tetrafluoroborate: Reagents for Stoichiometric Oxidations of Alcohols
10.1055/s-0032-1317861 · ExternalCitation · doi-reference
A comprehensive and updated review of studies on the oxidation of cyclohexane to produce ketone‐alcohol (KA) oil
10.1515/revce-2020-0059 · ExternalCitation · doi-reference
