Hypervalent iodine compounds are viable reagents for the oxidation of N,N-disubstituted hydroxylamines to the corresponding nitrones, with IBX performing best. The procedure is very simple and user-friendly and affords the target compounds with high efficiency and regioselectivity, highlighting IBX as the reagent of choice for preparation of aldonitrones from nonsymmetric hydroxylamines. Evidence for a mechanism involving nitrogen to iodine coordination has been collected.

Oxidation of N,N-Disubstituted Hydroxylamines to Nitrones with Hypervalent Iodine Reagents / Matassini, Camilla; Parmeggiani, Camilla; Cardona, Francesca; Goti, Andrea. - In: ORGANIC LETTERS. - ISSN 1523-7060. - STAMPA. - 17:(2015), pp. 4082-4085. [10.1021/acs.orglett.5b02029]

Oxidation of N,N-Disubstituted Hydroxylamines to Nitrones with Hypervalent Iodine Reagents

MATASSINI, CAMILLA
Membro del Collaboration Group
;
PARMEGGIANI, CAMILLA
Membro del Collaboration Group
;
CARDONA, FRANCESCA
Membro del Collaboration Group
;
GOTI, ANDREA
2015

Abstract

Hypervalent iodine compounds are viable reagents for the oxidation of N,N-disubstituted hydroxylamines to the corresponding nitrones, with IBX performing best. The procedure is very simple and user-friendly and affords the target compounds with high efficiency and regioselectivity, highlighting IBX as the reagent of choice for preparation of aldonitrones from nonsymmetric hydroxylamines. Evidence for a mechanism involving nitrogen to iodine coordination has been collected.
2015
17
4082
4085
Matassini, Camilla; Parmeggiani, Camilla; Cardona, Francesca; Goti, Andrea
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1010851
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