Cu(II)-Catalyzed Hydroboration Reactions of 1,1-Disubstituted α,β-Unsaturated Ketones, Esters, and Amides in Pure Water

被引:1
|
作者
Zhao, Xue [1 ]
Li, Weishuang [1 ]
Zhou, Lijie [1 ]
Zhao, Xuhong [1 ,2 ]
Zhang, Yaoyao [1 ]
Li, Bojie [1 ]
Li, Rong [2 ]
Zhu, Lei [1 ,2 ]
机构
[1] Hubei Engn Univ, Sch Chem & Mat Sci, Hubei Key Lab Qual Control Characterist Fruits & V, Xiaogan 432000, Peoples R China
[2] Hubei Univ, Sch Mat Sci & Engn, Minist Educ Key Lab Green Preparat & Applicat Func, Wuhan 430062, Peoples R China
来源
JOURNAL OF ORGANIC CHEMISTRY | 2024年 / 89卷 / 12期
基金
中国国家自然科学基金;
关键词
CATALYZED BETA-BORATION; ARYL-BORONIC ACIDS; CARBONYL-COMPOUNDS; ROOM-TEMPERATURE; ASYMMETRIC-SYNTHESIS; ARYLBORONIC ACIDS; N-ARYLATION; BORYLATION; BIS(PINACOLATO)DIBORON; NANOPARTICLES;
D O I
10.1021/acs.joc.3c02942
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Here, a Cu-2(OH)(2)CO3-catalyzed hydroboration reaction of 1,1-disubstituted alpha,beta-unsaturated compounds has been developed. The reaction was carried out using water as a solvent at room temperature except for N-monosubstituted alpha,beta-unsaturated amides. This method is applicable to diverse 1,1-disubstituted alpha,beta-unsaturated ketones, esters, and amides, showing excellent reactivity (up to 98% yield). Gram-scale experiments and functional group transformations further demonstrated the practicality of this method.
引用
收藏
页码:8334 / 8341
页数:8
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