![An effective and catalytic oxidation using recyclable fluorous IBX - Chemical Communications (RSC Publishing) DOI:10.1039/C0CC03149F An effective and catalytic oxidation using recyclable fluorous IBX - Chemical Communications (RSC Publishing) DOI:10.1039/C0CC03149F](https://pubs.rsc.org/image/article/2011/CC/c0cc03149f/c0cc03149f-s3.gif)
An effective and catalytic oxidation using recyclable fluorous IBX - Chemical Communications (RSC Publishing) DOI:10.1039/C0CC03149F
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
![IBX‐Mediated Dehydrogenation of Substituted β‐Oxonitriles - Klahn - 2014 - European Journal of Organic Chemistry - Wiley Online Library IBX‐Mediated Dehydrogenation of Substituted β‐Oxonitriles - Klahn - 2014 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/6facc37b-4582-4faa-987f-0d6d1cfbbabe/mfig000.jpg)
IBX‐Mediated Dehydrogenation of Substituted β‐Oxonitriles - Klahn - 2014 - European Journal of Organic Chemistry - 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 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)
New Reactions of IBX: Oxidation of Nitrogen‐ and Sulfur‐Containing Substrates To Afford Useful Synthetic Intermediates - Nicolaou - 2003 - Angewandte Chemie - Wiley Online Library
![Mechanistic investigation into phenol oxidation by IBX elucidated by DFT calculations - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C9OB02650A Mechanistic investigation into phenol oxidation by IBX elucidated by DFT calculations - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C9OB02650A](https://pubs.rsc.org/image/article/2020/OB/c9ob02650a/c9ob02650a-s4_hi-res.gif)
Mechanistic investigation into phenol oxidation by IBX elucidated by DFT calculations - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C9OB02650A
![2-Iodoxybenzoic Acid: An Oxidant for Functional Group Transformations : Oriental Journal of Chemistry 2-Iodoxybenzoic Acid: An Oxidant for Functional Group Transformations : Oriental Journal of Chemistry](http://www.orientjchem.org/wp-content/uploads/2020/10/Vol_36_No_5_Iod_Vip_Sch14.jpg)
2-Iodoxybenzoic Acid: An Oxidant for Functional Group Transformations : Oriental Journal of Chemistry
![Scheme 4. General mechanism of oxidation of primary alcohols with IBX. | Download Scientific Diagram Scheme 4. General mechanism of oxidation of primary alcohols with IBX. | Download Scientific Diagram](https://www.researchgate.net/publication/326308775/figure/fig1/AS:647009790881799@1531270563889/Scheme-4-General-mechanism-of-oxidation-of-primary-alcohols-with-IBX_Q320.jpg)
Scheme 4. General mechanism of oxidation of primary alcohols with IBX. | Download Scientific Diagram
![Oxidation of Silyl Enol Ethers by Using IBX and IBX⋅N‐Oxide Complexes: A Mild and Selective Reaction for the Synthesis of Enones - Nicolaou - 2002 - Angewandte Chemie International Edition - Wiley Online Library Oxidation of Silyl Enol Ethers by Using IBX and IBX⋅N‐Oxide Complexes: A Mild and Selective Reaction for the Synthesis of Enones - Nicolaou - 2002 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/2fdb5d34-bc61-4710-a8e1-bf01c9a67bfc/mcontent.jpg)
Oxidation of Silyl Enol Ethers by Using IBX and IBX⋅N‐Oxide Complexes: A Mild and Selective Reaction for the Synthesis of Enones - Nicolaou - 2002 - Angewandte Chemie International Edition - Wiley Online Library
![Figure 3 from Iodine(V) reagents in organic synthesis. Part 4. o-Iodoxybenzoic acid as a chemospecific tool for single electron transfer-based oxidation processes. | Semantic Scholar Figure 3 from Iodine(V) reagents in organic synthesis. Part 4. o-Iodoxybenzoic acid as a chemospecific tool for single electron transfer-based oxidation processes. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/a747336b131d8d3837b62e6cae8fdf3d561c22a2/6-Figure3-1.png)
Figure 3 from Iodine(V) reagents in organic synthesis. Part 4. o-Iodoxybenzoic acid as a chemospecific tool for single electron transfer-based oxidation processes. | Semantic Scholar
![2-Iodoxybenzoic Acid: An Oxidant for Functional Group Transformations : Oriental Journal of Chemistry 2-Iodoxybenzoic Acid: An Oxidant for Functional Group Transformations : Oriental Journal of Chemistry](http://www.orientjchem.org/wp-content/uploads/2020/10/Vol_36_No_5_Iod_Vip_Fig4.jpg)