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One-pot reductive amination of carbonyl compounds and nitro compounds via Ir-catalyzed transfer hydrogenation
The formation of C–N bond is a vital synthetic tool for establishing molecular diversity, which is highly sought after in a wide range of biologically active natural products and drugs. Herein, we present a new strategy for the synthesis of secondary amines via iridium-catalyzed one-pot reductive am...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10561669/ https://www.ncbi.nlm.nih.gov/pubmed/37818258 http://dx.doi.org/10.1039/d3ra05736d |
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author | Luo, Renshi Tong, Jinghui Ouyang, Lu Liu, Liang Liao, Jianhua |
author_facet | Luo, Renshi Tong, Jinghui Ouyang, Lu Liu, Liang Liao, Jianhua |
author_sort | Luo, Renshi |
collection | PubMed |
description | The formation of C–N bond is a vital synthetic tool for establishing molecular diversity, which is highly sought after in a wide range of biologically active natural products and drugs. Herein, we present a new strategy for the synthesis of secondary amines via iridium-catalyzed one-pot reductive amination of carbonyl compounds with nitro compounds. This method is demonstrated for a variety of carbonyl compounds, including miscellaneous aldehydes and ketones, which are compatible with this catalytic system, and deliver the desired products in good yields under mild conditions. In this protocol, the reduction of nitro compounds occurs in situ first, followed by reductive amination to form amine products, providing a new one-pot procedure for amine synthesis. |
format | Online Article Text |
id | pubmed-10561669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-105616692023-10-10 One-pot reductive amination of carbonyl compounds and nitro compounds via Ir-catalyzed transfer hydrogenation Luo, Renshi Tong, Jinghui Ouyang, Lu Liu, Liang Liao, Jianhua RSC Adv Chemistry The formation of C–N bond is a vital synthetic tool for establishing molecular diversity, which is highly sought after in a wide range of biologically active natural products and drugs. Herein, we present a new strategy for the synthesis of secondary amines via iridium-catalyzed one-pot reductive amination of carbonyl compounds with nitro compounds. This method is demonstrated for a variety of carbonyl compounds, including miscellaneous aldehydes and ketones, which are compatible with this catalytic system, and deliver the desired products in good yields under mild conditions. In this protocol, the reduction of nitro compounds occurs in situ first, followed by reductive amination to form amine products, providing a new one-pot procedure for amine synthesis. The Royal Society of Chemistry 2023-10-09 /pmc/articles/PMC10561669/ /pubmed/37818258 http://dx.doi.org/10.1039/d3ra05736d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Luo, Renshi Tong, Jinghui Ouyang, Lu Liu, Liang Liao, Jianhua One-pot reductive amination of carbonyl compounds and nitro compounds via Ir-catalyzed transfer hydrogenation |
title | One-pot reductive amination of carbonyl compounds and nitro compounds via Ir-catalyzed transfer hydrogenation |
title_full | One-pot reductive amination of carbonyl compounds and nitro compounds via Ir-catalyzed transfer hydrogenation |
title_fullStr | One-pot reductive amination of carbonyl compounds and nitro compounds via Ir-catalyzed transfer hydrogenation |
title_full_unstemmed | One-pot reductive amination of carbonyl compounds and nitro compounds via Ir-catalyzed transfer hydrogenation |
title_short | One-pot reductive amination of carbonyl compounds and nitro compounds via Ir-catalyzed transfer hydrogenation |
title_sort | one-pot reductive amination of carbonyl compounds and nitro compounds via ir-catalyzed transfer hydrogenation |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10561669/ https://www.ncbi.nlm.nih.gov/pubmed/37818258 http://dx.doi.org/10.1039/d3ra05736d |
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