LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Copper-catalyzed aerobic oxidative amination of arylboronic acid with aminal under base-free conditions
DepartmentOSSO国家重点实验室
Zhou YP(周艳平)1; Xie YJ(谢银君)2; Yang L(杨磊)2; Jie P(解攀)2; Huang HM(黄汉民)1,2; Huang HM(黄汉民)
2013
Source PublicationTetrahedron Letters
ISSN0040-4039
Volume54Issue:21Pages:2713-2716
AbstractA new process involving copper-catalyzed oxidative amination reaction of various arylboronic acids with aminals under mild conditions has been developed. The key copper-amide species involved in the C-N bond-forming process was generated via C-N bond cleavage of aminal under base-free conditions. Moderate yields of desired amination products can be obtained under mild conditions when air was served as oxidant and PhCO2H was used as an additive.
KeywordCopper Oxidative Amination C-n Cleavage Aminal Base-free
Subject Area物理化学与绿色催化
DOI10.1016/j.tetlet.2013.03.058
Funding Organizationthe National Natural Science Foundation of China (21172226;21133011;21222203);Chinese Academy of Sciences
Indexed BySCI
If2.391
Language英语
Funding Project有机功能材料研究组
compositor第二作者单位
Citation statistics
Cited Times:15[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/4631
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorHuang HM(黄汉民)
Affiliation1.Zhejiang Univ Technol, Coll Chem Engn & Mat Sci, Hangzhou 310014, Zhejiang, Peoples R China
2.Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
Recommended Citation
GB/T 7714
Zhou YP,Xie YJ,Yang L,et al. Copper-catalyzed aerobic oxidative amination of arylboronic acid with aminal under base-free conditions[J]. Tetrahedron Letters,2013,54(21):2713-2716.
APA Zhou YP,Xie YJ,Yang L,Jie P,Huang HM,&黄汉民.(2013).Copper-catalyzed aerobic oxidative amination of arylboronic acid with aminal under base-free conditions.Tetrahedron Letters,54(21),2713-2716.
MLA Zhou YP,et al."Copper-catalyzed aerobic oxidative amination of arylboronic acid with aminal under base-free conditions".Tetrahedron Letters 54.21(2013):2713-2716.
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