Triphenylbismuth carbonate-mediated oxidation of hydroxylamines to nitrones and in situ 1,3-dipolar cycloaddition
Author:
Affiliation:
1. Service de Chimie Bioorganique et de Marquage (SCBM)
2. CEA
3. Université Paris-Saclay
4. 91191 Gif-sur-Yvette
5. France
Abstract
Triphenylbismuth carbonate was shown to act as a mild, selective and efficient reagent for the oxidation of hydroxylamines.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2016/RA/C6RA18578A
Reference31 articles.
1. Bismuth in Organic Transformations
2. Functional group oxidation by pentavalent organobismuth reagents
3. J. P. Kitchin , in Organic Syntheses by Oxidation with Metal Compounds, ed. W. J. Mijs and C. R. H. I. De Jonge, Plenum Press, New York, 1986, p. 817
4. Arylation reactions with organobismuth reagents
5. µ-Oxo-bis(chlorotriphenylbismuth): a mild reagent for the oxidation of the hydroxy group, especially in allylic alcohols
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