One-pot reductive amination of carbonyl compounds and nitro compounds via Ir-catalyzed transfer hydrogenation

被引:2
|
作者
Luo, Renshi [1 ,2 ]
Tong, Jinghui [2 ]
Ouyang, Lu [2 ]
Liu, Liang [2 ]
Liao, Jianhua [2 ]
机构
[1] Shaoguan Univ, Coll Chem & Environm Engn, Shaoguan 512005, Peoples R China
[2] Gannan Med Univ, Sch Pharmaceut Sci, Ganzhou 341000, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
SECONDARY-AMINES; N-ALKYLATION; ALDEHYDES; NITROARENES; NANOPARTICLES; EFFICIENT; LIGANDS; KETONES; AMIDES;
D O I
10.1039/d3ra05736d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:29607 / 29612
页数:6
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