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A nickel phosphide nanoalloy catalyst for the C-3 alkylation of oxindoles with alcohols
Although transition metal phosphides are well studied as electrocatalysts and hydrotreating catalysts, the application of metal phosphides in organic synthesis is rare, and cooperative catalysis between metal phosphides and supports remains unexplored. Herein, we report that a cerium dioxide-support...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140154/ https://www.ncbi.nlm.nih.gov/pubmed/34021187 http://dx.doi.org/10.1038/s41598-021-89561-1 |
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author | Fujita, Shu Imagawa, Kohei Yamaguchi, Sho Yamasaki, Jun Yamazoe, Seiji Mizugaki, Tomoo Mitsudome, Takato |
author_facet | Fujita, Shu Imagawa, Kohei Yamaguchi, Sho Yamasaki, Jun Yamazoe, Seiji Mizugaki, Tomoo Mitsudome, Takato |
author_sort | Fujita, Shu |
collection | PubMed |
description | Although transition metal phosphides are well studied as electrocatalysts and hydrotreating catalysts, the application of metal phosphides in organic synthesis is rare, and cooperative catalysis between metal phosphides and supports remains unexplored. Herein, we report that a cerium dioxide-supported nickel phosphide nanoalloy (nano-Ni(2)P/CeO(2)) efficiently promoted the C-3 alkylation of oxindoles with alcohols without any additives through the borrowing hydrogen methodology. Oxindoles were alkylated with various alcohols to provide the corresponding C-3 alkylated oxindoles in high yields. This is the first catalytic system for the C-3 alkylation of oxindoles with alcohols using a non-precious metal-based heterogeneous catalyst. The catalytic activity of nano-Ni(2)P/CeO(2) was comparable to that reported for precious metal-based catalysts. Moreover, nano-Ni(2)P/CeO(2) was easily recoverable and reusable without any significant loss of activity. Control experiments revealed that the Ni(2)P nanoalloy and the CeO(2) support functioned cooperatively, leading to a high catalytic performance. |
format | Online Article Text |
id | pubmed-8140154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81401542021-05-25 A nickel phosphide nanoalloy catalyst for the C-3 alkylation of oxindoles with alcohols Fujita, Shu Imagawa, Kohei Yamaguchi, Sho Yamasaki, Jun Yamazoe, Seiji Mizugaki, Tomoo Mitsudome, Takato Sci Rep Article Although transition metal phosphides are well studied as electrocatalysts and hydrotreating catalysts, the application of metal phosphides in organic synthesis is rare, and cooperative catalysis between metal phosphides and supports remains unexplored. Herein, we report that a cerium dioxide-supported nickel phosphide nanoalloy (nano-Ni(2)P/CeO(2)) efficiently promoted the C-3 alkylation of oxindoles with alcohols without any additives through the borrowing hydrogen methodology. Oxindoles were alkylated with various alcohols to provide the corresponding C-3 alkylated oxindoles in high yields. This is the first catalytic system for the C-3 alkylation of oxindoles with alcohols using a non-precious metal-based heterogeneous catalyst. The catalytic activity of nano-Ni(2)P/CeO(2) was comparable to that reported for precious metal-based catalysts. Moreover, nano-Ni(2)P/CeO(2) was easily recoverable and reusable without any significant loss of activity. Control experiments revealed that the Ni(2)P nanoalloy and the CeO(2) support functioned cooperatively, leading to a high catalytic performance. Nature Publishing Group UK 2021-05-21 /pmc/articles/PMC8140154/ /pubmed/34021187 http://dx.doi.org/10.1038/s41598-021-89561-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Fujita, Shu Imagawa, Kohei Yamaguchi, Sho Yamasaki, Jun Yamazoe, Seiji Mizugaki, Tomoo Mitsudome, Takato A nickel phosphide nanoalloy catalyst for the C-3 alkylation of oxindoles with alcohols |
title | A nickel phosphide nanoalloy catalyst for the C-3 alkylation of oxindoles with alcohols |
title_full | A nickel phosphide nanoalloy catalyst for the C-3 alkylation of oxindoles with alcohols |
title_fullStr | A nickel phosphide nanoalloy catalyst for the C-3 alkylation of oxindoles with alcohols |
title_full_unstemmed | A nickel phosphide nanoalloy catalyst for the C-3 alkylation of oxindoles with alcohols |
title_short | A nickel phosphide nanoalloy catalyst for the C-3 alkylation of oxindoles with alcohols |
title_sort | nickel phosphide nanoalloy catalyst for the c-3 alkylation of oxindoles with alcohols |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140154/ https://www.ncbi.nlm.nih.gov/pubmed/34021187 http://dx.doi.org/10.1038/s41598-021-89561-1 |
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