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, CAMILLAMembro del Collaboration Group
;PARMEGGIANI, CAMILLAMembro del Collaboration Group
;CARDONA, FRANCESCAMembro 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.File | Dimensione | Formato | |
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