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Catalytic Version of and Reuse in Hypervalent Organo‐λ<sup>3</sup>‐ and ‐λ<sup>5</sup>‐iodane Oxidation
European Journal of Organic Chemistry · 2008 · Vol. 2008(25) · pp. 4229–4239
Masahito Ochiai✉(Tokushima University)Kazunori Miyamoto(Tokushima University)
Abstract
Abstract Hypervalent organoiodanes are one of the most valuable classes of oxidants for use in oxidative transformations of various kinds of functionalities in modern organic synthesis. This microreview provides an overview of the recently developed aryl iodide‐catalyzed oxidations, in which hypervalent organoiodanes(III and V) generated in situ serve as the actual oxidants. We also summarize recent attempts to improve the efficiency of recyclable hypervalent organoiodanes in oxidations, updating Togo's and Sakuratani's 2002 review.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)
Oxidative Organic Chemistry ReactionsSynthesis and Catalytic ReactionsVanadium and Halogenation ChemistryHypervalent moleculeChemistryCatalysisIodideReuseArylCombinatorial chemistryOrganic chemistryIodineAlkyl
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References
A Versatile and Highly Selective Hypervalent Iodine (III)/2,2,6,6-Tetramethyl-1-piperidinyloxyl-Mediated Oxidation of Alcohols to Carbonyl Compounds
The Journal of Organic Chemistry · 1997 · 758 citations
A User-Friendly Entry to 2-Iodoxybenzoic Acid (IBX)
The Journal of Organic Chemistry · 1999 · 645 citations
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