化学
吡啶
产量(工程)
催化作用
加合物
反应性(心理学)
联吡啶
组合化学
配体(生物化学)
对映选择合成
立体化学
药物化学
有机化学
受体
医学
生物化学
材料科学
替代医学
病理
晶体结构
冶金
作者
Shijie Zhu,Xue Tian,Jichang Liu,Bin Dai,Shiwu Li
出处
期刊:Organic Letters
[American Chemical Society]
日期:2024-04-18
卷期号:26 (17): 3487-3492
被引量:9
标识
DOI:10.1021/acs.orglett.4c00515
摘要
A novel type of highly efficient chiral C2-symmetric bipyridine-N,N'-dioxides ligand application in catalyzing Michael addition/Cyclization of 5-aminopyrazoles with α,β-unsaturated 2-acyl imidazoles has been developed, affording the corresponding adducts in 85-97% yield with up to 99% enantioselectivity under mild conditions with a lower catalyst loading and broad scope. Remarkably, this protocol exhibits advantages in terms of reactivity and enantioselectivity, giving the fact that as low as 2.2 mol % of L1 and 2.0 mol % of Ni(OTf)2 can promote the title reaction on gram scale to afford the desired product with excellent enantioselectivity.
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