Chemoselective preparation of 1,1-diacetates from aldehydes, mediated by a Keggin heteropolyacid under solvent free conditions at room temperature

A simple, general and efficient method has been developed for the conversion of aldehydes to 1,1-diacetates using acetic anhydride, a catalytic amount of non commercial Keggin heteropolyacid (H<SUB>6</SUB> PalMo<SUB>11</SUB>O<SUB>40</SUB>) (1% mol) in solvent free...

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Autores principales: Romanelli, Gustavo Pablo, Dimitroff, Pablo, Vázquez, Patricia Graciela, Autino, Juan Carlos
Formato: Articulo
Lenguaje:inglés
Publicado: 2007
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/40164
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author Romanelli, Gustavo Pablo
Dimitroff, Pablo
Vázquez, Patricia Graciela
Autino, Juan Carlos
author_facet Romanelli, Gustavo Pablo
Dimitroff, Pablo
Vázquez, Patricia Graciela
Autino, Juan Carlos
author_sort Romanelli, Gustavo Pablo
collection Repositorio Sedici - Comunidad
description A simple, general and efficient method has been developed for the conversion of aldehydes to 1,1-diacetates using acetic anhydride, a catalytic amount of non commercial Keggin heteropolyacid (H<SUB>6</SUB> PalMo<SUB>11</SUB>O<SUB>40</SUB>) (1% mol) in solvent free conditions at room temperature. Aromatic and aliphatic, simple and conjugated aldehydes were protected with excellent yields.
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spelling I89-R6-10915-401642026-02-24T17:25:06Z http://sedici.unlp.edu.ar/handle/10915/40164 Chemoselective preparation of 1,1-diacetates from aldehydes, mediated by a Keggin heteropolyacid under solvent free conditions at room temperature Romanelli, Gustavo Pablo Dimitroff, Pablo Vázquez, Patricia Graciela Autino, Juan Carlos 2007 2014-09-19T14:36:13Z en Ciencias Exactas Química 1,1-diacetates acylals aldehydes heteropolyacid Keggin catalyst solvent-free A simple, general and efficient method has been developed for the conversion of aldehydes to 1,1-diacetates using acetic anhydride, a catalytic amount of non commercial Keggin heteropolyacid (H<SUB>6</SUB> PalMo<SUB>11</SUB>O<SUB>40</SUB>) (1% mol) in solvent free conditions at room temperature. Aromatic and aliphatic, simple and conjugated aldehydes were protected with excellent yields. Facultad de Ciencias Exactas Articulo Articulo http://creativecommons.org/licenses/by/3.0/ Creative Commons Attribution 3.0 Unported (CC BY 3.0) application/pdf 83-89
spellingShingle Ciencias Exactas
Química
1,1-diacetates
acylals
aldehydes
heteropolyacid
Keggin catalyst
solvent-free
Romanelli, Gustavo Pablo
Dimitroff, Pablo
Vázquez, Patricia Graciela
Autino, Juan Carlos
Chemoselective preparation of 1,1-diacetates from aldehydes, mediated by a Keggin heteropolyacid under solvent free conditions at room temperature
title Chemoselective preparation of 1,1-diacetates from aldehydes, mediated by a Keggin heteropolyacid under solvent free conditions at room temperature
title_full Chemoselective preparation of 1,1-diacetates from aldehydes, mediated by a Keggin heteropolyacid under solvent free conditions at room temperature
title_fullStr Chemoselective preparation of 1,1-diacetates from aldehydes, mediated by a Keggin heteropolyacid under solvent free conditions at room temperature
title_full_unstemmed Chemoselective preparation of 1,1-diacetates from aldehydes, mediated by a Keggin heteropolyacid under solvent free conditions at room temperature
title_short Chemoselective preparation of 1,1-diacetates from aldehydes, mediated by a Keggin heteropolyacid under solvent free conditions at room temperature
title_sort chemoselective preparation of 1 1 diacetates from aldehydes mediated by a keggin heteropolyacid under solvent free conditions at room temperature
topic Ciencias Exactas
Química
1,1-diacetates
acylals
aldehydes
heteropolyacid
Keggin catalyst
solvent-free
url http://sedici.unlp.edu.ar/handle/10915/40164
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