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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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Detalles Bibliográficos
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
Descripción
Sumario: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.