中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Diastereoselective Electrophilic alpha-Hydroxyamination of N-tert-Butanesulfinyl lmidates

文献类型:期刊论文

作者Ma, PJ (Ma, Peng-Ju)[ 1,2 ]; Liu, H (Liu, Hui)[ 1 ]; Lu, CD (Lu, Chong-Dao)[ 1 ]; Xu, YJ (Xu, Yan-Jun)[ 1 ]
刊名ORGANIC LETTERS
出版日期2017
卷号19期号:3页码:670-673
DOI10.1021/acs.orglett.6b03835
英文摘要

Diastereoselective alpha-hydroxyamination of N-tert-butanesulfmyl imidates using nitrosoarenes is reported. A catalytic amount of base effectively promotes the hydroxyamination reaction of alpha-aryl-substituted imidates, and the resulting a-hydroxyamino imidates can be transformed into a range of synthetically useful intermediates.

WOS记录号WOS:000393539900062
源URL[http://ir.xjipc.cas.cn/handle/365002/5788]  
专题新疆理化技术研究所_省部共建新疆特有药用资源利用重点实验室
作者单位1.Chinese Acad Sci, Key Lab Plant Resources & Chem Arid Zones, Xinjiang Tech Inst Phys & Chem, Urumqi 830011, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
推荐引用方式
GB/T 7714
Ma, PJ ,Liu, H ,Lu, CD ,et al. Diastereoselective Electrophilic alpha-Hydroxyamination of N-tert-Butanesulfinyl lmidates[J]. ORGANIC LETTERS,2017,19(3):670-673.
APA Ma, PJ ,Liu, H ,Lu, CD ,&Xu, YJ .(2017).Diastereoselective Electrophilic alpha-Hydroxyamination of N-tert-Butanesulfinyl lmidates.ORGANIC LETTERS,19(3),670-673.
MLA Ma, PJ ,et al."Diastereoselective Electrophilic alpha-Hydroxyamination of N-tert-Butanesulfinyl lmidates".ORGANIC LETTERS 19.3(2017):670-673.

入库方式: OAI收割

来源:新疆理化技术研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。