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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...

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Autores principales: Luo, Renshi, Tong, Jinghui, Ouyang, Lu, Liu, Liang, Liao, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
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.
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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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