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Open AccessArticle

Metathetical Redox Reaction of (Diacetoxyiodo)arenes and Iodoarenes

Centre in Green Chemistry and Catalysis, Department of Chemistry, University of Sherbrooke, 2500 boul. de l’Université, Sherbrooke, QC J1K 2R1, Canada
Author to whom correspondence should be addressed.
Academic Editors: Wesley Moran and Arantxa Rodríguez
Molecules 2015, 20(12), 22635-22644;
Received: 25 November 2015 / Revised: 10 December 2015 / Accepted: 15 December 2015 / Published: 17 December 2015
(This article belongs to the Special Issue Hypervalent Iodine Chemistry)
The oxidation of iodoarenes is central to the field of hypervalent iodine chemistry. It was found that the metathetical redox reaction between (diacetoxyiodo)arenes and iodoarenes is possible in the presence of a catalytic amount of Lewis acid. This discovery opens a new strategy to access (diacetoxyiodo)arenes. A computational study is provided to rationalize the results observed. View Full-Text
Keywords: hypervalent iodine; (diacetoxyiodo)arenes; metathesis hypervalent iodine; (diacetoxyiodo)arenes; metathesis
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MDPI and ACS Style

Jobin-Des Lauriers, A.; Legault, C.Y. Metathetical Redox Reaction of (Diacetoxyiodo)arenes and Iodoarenes. Molecules 2015, 20, 22635-22644.

AMA Style

Jobin-Des Lauriers A, Legault CY. Metathetical Redox Reaction of (Diacetoxyiodo)arenes and Iodoarenes. Molecules. 2015; 20(12):22635-22644.

Chicago/Turabian Style

Jobin-Des Lauriers, Antoine; Legault, Claude Y. 2015. "Metathetical Redox Reaction of (Diacetoxyiodo)arenes and Iodoarenes" Molecules 20, no. 12: 22635-22644.

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