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Molecules 2008, 13(6), 1230-1237; doi:10.3390/molecules13061230

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

Dipartimento di Scienze Chimiche, Università di Catania, Viale Andrea Doria 6, Catania 95125, Italy
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Received: 29 April 2008 / Revised: 12 May 2008 / Accepted: 15 May 2008 / Published: 1 June 2008
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Abstract

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. View Full-Text
Keywords: Oxidation of oximes; oxodiperoxotungsto complex; 1; 3-dipolar cycloaddition; nitrile oxides; aldehydes. Oxidation of oximes; oxodiperoxotungsto complex; 1; 3-dipolar cycloaddition; nitrile oxides; aldehydes.
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

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MDPI and ACS Style

Ballistreri, F.P.; Chiacchio, U.; Rescifina, A.; Tomaselli, G.; Toscano, R.M. Conversion of Oximes to Carbonyl Compounds by Triscetylpyridinium Tetrakis(oxodiperoxotungsto) Phosphate (PCWP)-mediated Oxidation with Hydrogen Peroxide. Molecules 2008, 13, 1230-1237.

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