Aminoazanium of DABCO: An Amination Reagent for Alkyl and Aryl Pinacol Boronates

被引:61
|
作者
Liu, Xingxing [1 ,2 ]
Zhu, Qing [2 ,4 ]
Chen, Du [2 ,4 ]
Wang, Lu [2 ]
Jin, Liqun [1 ]
Liu, Chao [2 ,3 ]
机构
[1] Zhejiang Univ Technol, Coll Chem Engn, Hangzhou 310014, Peoples R China
[2] Chinese Acad Sci, Suzhou Res Inst, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
[3] Hangzhou Normal Univ, Minist Educ, Key Lab Organosilicon Chem & Mat Technol, Hangzhou 311121, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
amination; arenes; amines; boron; synthetic methods; BORONIC ACIDS; STEREOSPECIFIC SYNTHESIS; SECONDARY-AMINES; CHIRAL SYNTHESIS; FREE DIBORATION; ORGANIC AZIDES; METAL; ORGANOBORANES; ACCESS; ALKYLDICHLOROBORANES;
D O I
10.1002/anie.201913388
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The aminoazanium of DABCO (H2N-DABCO) has been developed as a general and practical amination reagent for the direct amination of alkyl and aryl pinacol boronates. This compound is stable and practical for use as a reagent. Various primary, secondary. and tertiary alkyl-Bpin and aryl-Bpin substrates were aminated to give the corresponding amine derivatives. The amination is stereospecific. The anti-Markovnikov hydroamination of olefins was easily achieved by catalytic hydroboration with HBpin and in subsequent situ amination using H2N-DABCO. Moreover, the combination of 1,2-diboration of olefins, using B(2)pin(2), with this amination process achieved the unprecedented 1,2-diamination of olefins. The amination protocol was also successfully extended to aryl pinacol boronates.
引用
收藏
页码:2745 / 2749
页数:5
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