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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MDPI AG
2008-06-01
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Online Access: | http://www.mdpi.com/1420-3049/13/6/1230/ |
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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/ |
work_keys_str_mv |
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