化学
催化作用
氘
镍
配体(生物化学)
氢
密度泛函理论
乙醇
营业额
功能群
组合化学
计算化学
有机化学
受体
生物化学
物理
量子力学
聚合物
作者
Dawei Gong,Degong Kong,Yufei Li,Caiyu Gao,Lina Zhao
出处
期刊:Organic Letters
[American Chemical Society]
日期:2023-05-31
卷期号:25 (22): 4198-4202
被引量:12
标识
DOI:10.1021/acs.orglett.3c01529
摘要
A nickel-catalyzed semihydrogenation of azoarenes to hydrazoarenes with NH3BH3 is developed. The catalytic system exhibits good functional group tolerance and a high turnover frequency at room temperature. Results of control and deuterium-labeling experiments indicate that the ethanol hydroxyl and BH3 groups each donated one hydrogen to this transfer hydrogenation, and the main byproducts were B(OEt)3 and H2. Moreover, density functional theory calculations indicated that the reaction proceeded via a ligand-to-ligand hydrogen transfer mechanism. This study presents a novel nickel catalytic system for the semihydrogenation of azoarenes.
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