Triphenylbismuth carbonate-mediated oxidation of hydroxylamines to nitrones and in situ 1,3-dipolar cycloaddition

Triphenylbismuth carbonate was shown to act as a mild, selective and efficient reagent for the oxidation of hydroxylamines. The developed reaction conditions were shown to be compatible with the in situ trapping of the produced nitrones by a strained alkyne, via a [3 + 2] cycloaddition reaction.

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Veröffentlicht in:RSC advances 2016-01, Vol.6 (92), p.89238-89241
Hauptverfasser: Nguyen, Dinh-Vu, Prakash, Praveen, Gravel, Edmond, Doris, Eric
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container_title RSC advances
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creator Nguyen, Dinh-Vu
Prakash, Praveen
Gravel, Edmond
Doris, Eric
description Triphenylbismuth carbonate was shown to act as a mild, selective and efficient reagent for the oxidation of hydroxylamines. The developed reaction conditions were shown to be compatible with the in situ trapping of the produced nitrones by a strained alkyne, via a [3 + 2] cycloaddition reaction.
doi_str_mv 10.1039/C6RA18578A
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source Royal Society Of Chemistry Journals 2008-
subjects Alkynes
Carbonates
Compatibility
Cycloaddition
Oxidation
Reagents
Trapping
title Triphenylbismuth carbonate-mediated oxidation of hydroxylamines to nitrones and in situ 1,3-dipolar cycloaddition
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