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Oxidative N-Formylation of Secondary Amines Catalyzed by Reusable Bimetallic AuPd–Fe(3)O(4) Nanoparticles
Bimetallic catalysts are gaining attention due to their characteristics of promoting reactivity and selectivity in catalyzed reactions. Herein, a new catalytic N-formylation of secondary amines using AuPd–Fe(3)O(4) at room temperature is reported. Methanol was utilized as the formyl source and 1.0 a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8400704/ https://www.ncbi.nlm.nih.gov/pubmed/34443931 http://dx.doi.org/10.3390/nano11082101 |
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author | Yang, Sabyuk Cho, Ahra Cho, Jin Hee Kim, Byeong Moon |
author_facet | Yang, Sabyuk Cho, Ahra Cho, Jin Hee Kim, Byeong Moon |
author_sort | Yang, Sabyuk |
collection | PubMed |
description | Bimetallic catalysts are gaining attention due to their characteristics of promoting reactivity and selectivity in catalyzed reactions. Herein, a new catalytic N-formylation of secondary amines using AuPd–Fe(3)O(4) at room temperature is reported. Methanol was utilized as the formyl source and 1.0 atm of O(2) gas served as an external oxidant. The bimetallic catalyst, consisting of Au and Pd, makes the reaction more efficient than that using each metal separately. In addition, the catalyst can be effectively recycled owing to the Fe(3)O(4) support. |
format | Online Article Text |
id | pubmed-8400704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84007042021-08-29 Oxidative N-Formylation of Secondary Amines Catalyzed by Reusable Bimetallic AuPd–Fe(3)O(4) Nanoparticles Yang, Sabyuk Cho, Ahra Cho, Jin Hee Kim, Byeong Moon Nanomaterials (Basel) Article Bimetallic catalysts are gaining attention due to their characteristics of promoting reactivity and selectivity in catalyzed reactions. Herein, a new catalytic N-formylation of secondary amines using AuPd–Fe(3)O(4) at room temperature is reported. Methanol was utilized as the formyl source and 1.0 atm of O(2) gas served as an external oxidant. The bimetallic catalyst, consisting of Au and Pd, makes the reaction more efficient than that using each metal separately. In addition, the catalyst can be effectively recycled owing to the Fe(3)O(4) support. MDPI 2021-08-18 /pmc/articles/PMC8400704/ /pubmed/34443931 http://dx.doi.org/10.3390/nano11082101 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yang, Sabyuk Cho, Ahra Cho, Jin Hee Kim, Byeong Moon Oxidative N-Formylation of Secondary Amines Catalyzed by Reusable Bimetallic AuPd–Fe(3)O(4) Nanoparticles |
title | Oxidative N-Formylation of Secondary Amines Catalyzed by Reusable Bimetallic AuPd–Fe(3)O(4) Nanoparticles |
title_full | Oxidative N-Formylation of Secondary Amines Catalyzed by Reusable Bimetallic AuPd–Fe(3)O(4) Nanoparticles |
title_fullStr | Oxidative N-Formylation of Secondary Amines Catalyzed by Reusable Bimetallic AuPd–Fe(3)O(4) Nanoparticles |
title_full_unstemmed | Oxidative N-Formylation of Secondary Amines Catalyzed by Reusable Bimetallic AuPd–Fe(3)O(4) Nanoparticles |
title_short | Oxidative N-Formylation of Secondary Amines Catalyzed by Reusable Bimetallic AuPd–Fe(3)O(4) Nanoparticles |
title_sort | oxidative n-formylation of secondary amines catalyzed by reusable bimetallic aupd–fe(3)o(4) nanoparticles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8400704/ https://www.ncbi.nlm.nih.gov/pubmed/34443931 http://dx.doi.org/10.3390/nano11082101 |
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