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Mn(III)-Initiated Facile Oxygenation of Heterocyclic 1,3-Dicarbonyl Compounds

The Mn(III)-initiated aerobic oxidation of heterocyclic 1,3-dicarbonyl compounds, such as 4-alkyl-1,2-diphenylpyrazolidine-3,5-diones, 1,3-dialkylpyrrolidine-2,4-diones, 3-alkyl-1,5-dimethylbarbituric acids, and 3-butyl-4-hydroxy-2-quinolinone gave excellent to good yields of the corresponding hydro...

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Detalles Bibliográficos
Autores principales: Rahman, Md. Taifur, Haque, Md. Aminul, Igarashi, Hikaru, Nishino, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264282/
https://www.ncbi.nlm.nih.gov/pubmed/22089863
http://dx.doi.org/10.3390/molecules16119562
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author Rahman, Md. Taifur
Haque, Md. Aminul
Igarashi, Hikaru
Nishino, Hiroshi
author_facet Rahman, Md. Taifur
Haque, Md. Aminul
Igarashi, Hikaru
Nishino, Hiroshi
author_sort Rahman, Md. Taifur
collection PubMed
description The Mn(III)-initiated aerobic oxidation of heterocyclic 1,3-dicarbonyl compounds, such as 4-alkyl-1,2-diphenylpyrazolidine-3,5-diones, 1,3-dialkylpyrrolidine-2,4-diones, 3-alkyl-1,5-dimethylbarbituric acids, and 3-butyl-4-hydroxy-2-quinolinone gave excellent to good yields of the corresponding hydroperoxides, which were gradually degraded by exposure to the metal initiator after the reaction to afford the corresponding alcohols. The synthesis of 30 heterocyclic 1,3-dicarbonyl compounds, the corresponding hydroperoxides and the 10 alcohols, their characterization, and the limitations of the procedure are described. In addition, the mechanism of the hydroperoxidation and the redox decomposition of the hydroperoxides are discussed.
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spelling pubmed-62642822018-12-10 Mn(III)-Initiated Facile Oxygenation of Heterocyclic 1,3-Dicarbonyl Compounds Rahman, Md. Taifur Haque, Md. Aminul Igarashi, Hikaru Nishino, Hiroshi Molecules Article The Mn(III)-initiated aerobic oxidation of heterocyclic 1,3-dicarbonyl compounds, such as 4-alkyl-1,2-diphenylpyrazolidine-3,5-diones, 1,3-dialkylpyrrolidine-2,4-diones, 3-alkyl-1,5-dimethylbarbituric acids, and 3-butyl-4-hydroxy-2-quinolinone gave excellent to good yields of the corresponding hydroperoxides, which were gradually degraded by exposure to the metal initiator after the reaction to afford the corresponding alcohols. The synthesis of 30 heterocyclic 1,3-dicarbonyl compounds, the corresponding hydroperoxides and the 10 alcohols, their characterization, and the limitations of the procedure are described. In addition, the mechanism of the hydroperoxidation and the redox decomposition of the hydroperoxides are discussed. MDPI 2011-11-16 /pmc/articles/PMC6264282/ /pubmed/22089863 http://dx.doi.org/10.3390/molecules16119562 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Rahman, Md. Taifur
Haque, Md. Aminul
Igarashi, Hikaru
Nishino, Hiroshi
Mn(III)-Initiated Facile Oxygenation of Heterocyclic 1,3-Dicarbonyl Compounds
title Mn(III)-Initiated Facile Oxygenation of Heterocyclic 1,3-Dicarbonyl Compounds
title_full Mn(III)-Initiated Facile Oxygenation of Heterocyclic 1,3-Dicarbonyl Compounds
title_fullStr Mn(III)-Initiated Facile Oxygenation of Heterocyclic 1,3-Dicarbonyl Compounds
title_full_unstemmed Mn(III)-Initiated Facile Oxygenation of Heterocyclic 1,3-Dicarbonyl Compounds
title_short Mn(III)-Initiated Facile Oxygenation of Heterocyclic 1,3-Dicarbonyl Compounds
title_sort mn(iii)-initiated facile oxygenation of heterocyclic 1,3-dicarbonyl compounds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264282/
https://www.ncbi.nlm.nih.gov/pubmed/22089863
http://dx.doi.org/10.3390/molecules16119562
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