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A bifunctional cerium phosphate catalyst for chemoselective acetalization

Acid–base solid catalysts synthesized with structurally controlled uniform active sites can lead to unique catalysis. In this study, a CePO(4) catalyst was synthesized using a hydrothermal method and found to exhibit high catalytic performance for the chemoselective acetalization of 5-hydroxymethylf...

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Autores principales: Kanai, Shunsuke, Nagahara, Ippei, Kita, Yusuke, Kamata, Keigo, Hara, Michikazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413973/
https://www.ncbi.nlm.nih.gov/pubmed/28507690
http://dx.doi.org/10.1039/c6sc05642c
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author Kanai, Shunsuke
Nagahara, Ippei
Kita, Yusuke
Kamata, Keigo
Hara, Michikazu
author_facet Kanai, Shunsuke
Nagahara, Ippei
Kita, Yusuke
Kamata, Keigo
Hara, Michikazu
author_sort Kanai, Shunsuke
collection PubMed
description Acid–base solid catalysts synthesized with structurally controlled uniform active sites can lead to unique catalysis. In this study, a CePO(4) catalyst was synthesized using a hydrothermal method and found to exhibit high catalytic performance for the chemoselective acetalization of 5-hydroxymethylfurfural with alcohols, in sharp contrast to other homogeneous and heterogeneous acid and/or base catalysts. In the presence of CePO(4), various combinations of carbonyl compounds and alcohols are efficiently converted into the corresponding acetal derivatives in good to excellent yields. Mechanistic studies show that CePO(4) most likely acts as a bifunctional catalyst through the interaction of uniform Lewis acid and weak base sites with 5-hydroxymethylfurfural and alcohol molecules, respectively, which results in high catalytic performance.
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spelling pubmed-54139732017-05-15 A bifunctional cerium phosphate catalyst for chemoselective acetalization Kanai, Shunsuke Nagahara, Ippei Kita, Yusuke Kamata, Keigo Hara, Michikazu Chem Sci Chemistry Acid–base solid catalysts synthesized with structurally controlled uniform active sites can lead to unique catalysis. In this study, a CePO(4) catalyst was synthesized using a hydrothermal method and found to exhibit high catalytic performance for the chemoselective acetalization of 5-hydroxymethylfurfural with alcohols, in sharp contrast to other homogeneous and heterogeneous acid and/or base catalysts. In the presence of CePO(4), various combinations of carbonyl compounds and alcohols are efficiently converted into the corresponding acetal derivatives in good to excellent yields. Mechanistic studies show that CePO(4) most likely acts as a bifunctional catalyst through the interaction of uniform Lewis acid and weak base sites with 5-hydroxymethylfurfural and alcohol molecules, respectively, which results in high catalytic performance. Royal Society of Chemistry 2017-04-01 2017-02-07 /pmc/articles/PMC5413973/ /pubmed/28507690 http://dx.doi.org/10.1039/c6sc05642c Text en This journal is © The Royal Society of Chemistry 2017 https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Kanai, Shunsuke
Nagahara, Ippei
Kita, Yusuke
Kamata, Keigo
Hara, Michikazu
A bifunctional cerium phosphate catalyst for chemoselective acetalization
title A bifunctional cerium phosphate catalyst for chemoselective acetalization
title_full A bifunctional cerium phosphate catalyst for chemoselective acetalization
title_fullStr A bifunctional cerium phosphate catalyst for chemoselective acetalization
title_full_unstemmed A bifunctional cerium phosphate catalyst for chemoselective acetalization
title_short A bifunctional cerium phosphate catalyst for chemoselective acetalization
title_sort bifunctional cerium phosphate catalyst for chemoselective acetalization
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413973/
https://www.ncbi.nlm.nih.gov/pubmed/28507690
http://dx.doi.org/10.1039/c6sc05642c
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