![o-Iodoxybenzoic Acid (IBX) as a Viable Reagent in the Manipulation of Nitrogen- and Sulfur-Containing Substrates: Scope, Generality, and Mechanism of IBX-Mediated Amine Oxidations and Dithiane Deprotections | Journal of the American Chemical o-Iodoxybenzoic Acid (IBX) as a Viable Reagent in the Manipulation of Nitrogen- and Sulfur-Containing Substrates: Scope, Generality, and Mechanism of IBX-Mediated Amine Oxidations and Dithiane Deprotections | Journal of the American Chemical](https://pubs.acs.org/cms/10.1021/ja0400382/asset/images/large/ja0400382n00001.jpeg)
o-Iodoxybenzoic Acid (IBX) as a Viable Reagent in the Manipulation of Nitrogen- and Sulfur-Containing Substrates: Scope, Generality, and Mechanism of IBX-Mediated Amine Oxidations and Dithiane Deprotections | Journal of the American Chemical
![o‐Iodoxybenzoic Acid (IBX): pKa and Proton‐Affinity Analysis - Gallen - 2006 - Angewandte Chemie - Wiley Online Library o‐Iodoxybenzoic Acid (IBX): pKa and Proton‐Affinity Analysis - Gallen - 2006 - Angewandte Chemie - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/c23f3305-1d2e-4dc8-ab00-6bae4aaa1c84/msch002.gif)
o‐Iodoxybenzoic Acid (IBX): pKa and Proton‐Affinity Analysis - Gallen - 2006 - Angewandte Chemie - Wiley Online Library
![Modulation of the Reactivity Profile of IBX by Ligand Complexation: Ambient Temperature Dehydrogenation of Aldehydes and Ketones to α,β‐Unsaturated Carbonyl Compounds - Nicolaou - 2002 - Angewandte Chemie International Edition - Wiley Online Library Modulation of the Reactivity Profile of IBX by Ligand Complexation: Ambient Temperature Dehydrogenation of Aldehydes and Ketones to α,β‐Unsaturated Carbonyl Compounds - Nicolaou - 2002 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/c1c3612b-9e52-4c98-bb90-aa4a9ac29728/mfig002.jpg)
Modulation of the Reactivity Profile of IBX by Ligand Complexation: Ambient Temperature Dehydrogenation of Aldehydes and Ketones to α,β‐Unsaturated Carbonyl Compounds - Nicolaou - 2002 - Angewandte Chemie International Edition - Wiley Online Library
Esters of 2-Iodoxybenzoic Acid: Hypervalent Iodine Oxidizing Reagents with a Pseudobenziodoxole Structure | The Journal of Organic Chemistry
![o‐Iodoxybenzoic Acid (IBX): pKa and Proton‐Affinity Analysis - Gallen - 2006 - Angewandte Chemie - Wiley Online Library o‐Iodoxybenzoic Acid (IBX): pKa and Proton‐Affinity Analysis - Gallen - 2006 - Angewandte Chemie - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/ea3590a4-3763-4fce-bafc-89a02fbc9bcb/mfor001.gif)
o‐Iodoxybenzoic Acid (IBX): pKa and Proton‐Affinity Analysis - Gallen - 2006 - Angewandte Chemie - Wiley Online Library
![Hypervalent Iodine Oxidants: Structure and Kinetics of the Reactive Intermediates in the Oxidation of Alcohols and 1,2-Diols by o-Iodoxybenzoic Acid (IBX) and Dess−Martin Periodinane. A Comparative 1H-NMR Study | The Journal of Hypervalent Iodine Oxidants: Structure and Kinetics of the Reactive Intermediates in the Oxidation of Alcohols and 1,2-Diols by o-Iodoxybenzoic Acid (IBX) and Dess−Martin Periodinane. A Comparative 1H-NMR Study | The Journal of](https://pubs.acs.org/cms/10.1021/jo961044m/asset/images/medium/jo961044mn00001.gif)
Hypervalent Iodine Oxidants: Structure and Kinetics of the Reactive Intermediates in the Oxidation of Alcohols and 1,2-Diols by o-Iodoxybenzoic Acid (IBX) and Dess−Martin Periodinane. A Comparative 1H-NMR Study | The Journal of
![New Synthetic Approach for the Construction of Multisubstituted 2‐Acyl Furans by the IBX‐Mediated Cascade Oxidation/Cyclization of cis‐2‐En‐4‐yn‐1‐ols (IBX=2‐Iodoxybenzoic Acid) - Du - 2008 - Chemistry – A European Journal - Wiley Online New Synthetic Approach for the Construction of Multisubstituted 2‐Acyl Furans by the IBX‐Mediated Cascade Oxidation/Cyclization of cis‐2‐En‐4‐yn‐1‐ols (IBX=2‐Iodoxybenzoic Acid) - Du - 2008 - Chemistry – A European Journal - Wiley Online](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/9803cc89-0bed-46b9-99fd-860274a99eca/msch001.gif)
New Synthetic Approach for the Construction of Multisubstituted 2‐Acyl Furans by the IBX‐Mediated Cascade Oxidation/Cyclization of cis‐2‐En‐4‐yn‐1‐ols (IBX=2‐Iodoxybenzoic Acid) - Du - 2008 - Chemistry – A European Journal - Wiley Online
2-Iodoxybenzoic acid is used in organic synthesis as an oxidizing agent. This periodinane is especially suited to oxidize alcohols to aldehydes. IBX is prepared from 2-iodobenzoic acid, potassium bromate, and sulfuric acid. #
![A Twist of the Twist Mechanism, 2-Iodoxybenzoic Acid (IBX)-Mediated Oxidation of Alcohol Revisited: Theory and Experiment | Organic Letters A Twist of the Twist Mechanism, 2-Iodoxybenzoic Acid (IBX)-Mediated Oxidation of Alcohol Revisited: Theory and Experiment | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.7b03167/asset/images/medium/ol-2017-03167r_0003.gif)
A Twist of the Twist Mechanism, 2-Iodoxybenzoic Acid (IBX)-Mediated Oxidation of Alcohol Revisited: Theory and Experiment | Organic Letters
![New Reactions of IBX: Oxidation of Nitrogen‐ and Sulfur‐Containing Substrates To Afford Useful Synthetic Intermediates - Nicolaou - 2003 - Angewandte Chemie - Wiley Online Library New Reactions of IBX: Oxidation of Nitrogen‐ and Sulfur‐Containing Substrates To Afford Useful Synthetic Intermediates - Nicolaou - 2003 - Angewandte Chemie - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/d56fdf1c-54a7-4567-8f38-a6eeb394e463/msch001.jpg)