Conversion of Oximes to Carbonyl Compounds by Triscetylpyridinium Tetrakis(oxodiperoxotungsto) Phosphate (PCWP)-mediated Oxidation with Hydrogen Peroxide

Aromatic and aliphatic oximes have been deoximated in chloroform-water to the corresponding aldehydes with dilute hydrogen peroxide and triscetylpyridinium tetrakis (oxodiperoxotungsto) phosphate as catalyst. The presence of dipolarophiles in the reaction mixtures allows a competitive reaction that...

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Main Authors: Rosa M. Toscano, Gaetano Tomaselli, Antonio Rescifina, Ugo Chiacchio, Francesco P. Ballistreri
Format: Article
Language:English
Published: MDPI AG 2008-06-01
Series:Molecules
Subjects:
1
Online Access:http://www.mdpi.com/1420-3049/13/6/1230/
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spelling doaj-6d8d98b276f14de4b75acc0c26afb5f12020-11-25T02:18:04ZengMDPI AGMolecules1420-30492008-06-011361230123710.3390/molecules13061230Conversion of Oximes to Carbonyl Compounds by Triscetylpyridinium Tetrakis(oxodiperoxotungsto) Phosphate (PCWP)-mediated Oxidation with Hydrogen PeroxideRosa M. ToscanoGaetano TomaselliAntonio RescifinaUgo ChiacchioFrancesco P. BallistreriAromatic and aliphatic oximes have been deoximated in chloroform-water to the corresponding aldehydes with dilute hydrogen peroxide and triscetylpyridinium tetrakis (oxodiperoxotungsto) phosphate as catalyst. The presence of dipolarophiles in the reaction mixtures allows a competitive reaction that converts oximes into isoxazole and isoxazoline derivatives via the intermediate formation of nitrile oxide species.http://www.mdpi.com/1420-3049/13/6/1230/Oxidation of oximesoxodiperoxotungsto complex13-dipolar cycloadditionnitrile oxidesaldehydes.
collection DOAJ
language English
format Article
sources DOAJ
author Rosa M. Toscano
Gaetano Tomaselli
Antonio Rescifina
Ugo Chiacchio
Francesco P. Ballistreri
spellingShingle Rosa M. Toscano
Gaetano Tomaselli
Antonio Rescifina
Ugo Chiacchio
Francesco P. Ballistreri
Conversion of Oximes to Carbonyl Compounds by Triscetylpyridinium Tetrakis(oxodiperoxotungsto) Phosphate (PCWP)-mediated Oxidation with Hydrogen Peroxide
Molecules
Oxidation of oximes
oxodiperoxotungsto complex
1
3-dipolar cycloaddition
nitrile oxides
aldehydes.
author_facet Rosa M. Toscano
Gaetano Tomaselli
Antonio Rescifina
Ugo Chiacchio
Francesco P. Ballistreri
author_sort Rosa M. Toscano
title Conversion of Oximes to Carbonyl Compounds by Triscetylpyridinium Tetrakis(oxodiperoxotungsto) Phosphate (PCWP)-mediated Oxidation with Hydrogen Peroxide
title_short Conversion of Oximes to Carbonyl Compounds by Triscetylpyridinium Tetrakis(oxodiperoxotungsto) Phosphate (PCWP)-mediated Oxidation with Hydrogen Peroxide
title_full Conversion of Oximes to Carbonyl Compounds by Triscetylpyridinium Tetrakis(oxodiperoxotungsto) Phosphate (PCWP)-mediated Oxidation with Hydrogen Peroxide
title_fullStr Conversion of Oximes to Carbonyl Compounds by Triscetylpyridinium Tetrakis(oxodiperoxotungsto) Phosphate (PCWP)-mediated Oxidation with Hydrogen Peroxide
title_full_unstemmed Conversion of Oximes to Carbonyl Compounds by Triscetylpyridinium Tetrakis(oxodiperoxotungsto) Phosphate (PCWP)-mediated Oxidation with Hydrogen Peroxide
title_sort conversion of oximes to carbonyl compounds by triscetylpyridinium tetrakis(oxodiperoxotungsto) phosphate (pcwp)-mediated oxidation with hydrogen peroxide
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2008-06-01
description Aromatic and aliphatic oximes have been deoximated in chloroform-water to the corresponding aldehydes with dilute hydrogen peroxide and triscetylpyridinium tetrakis (oxodiperoxotungsto) phosphate as catalyst. The presence of dipolarophiles in the reaction mixtures allows a competitive reaction that converts oximes into isoxazole and isoxazoline derivatives via the intermediate formation of nitrile oxide species.
topic Oxidation of oximes
oxodiperoxotungsto complex
1
3-dipolar cycloaddition
nitrile oxides
aldehydes.
url http://www.mdpi.com/1420-3049/13/6/1230/
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