Diastereoselective Electrophilic alpha-Hydroxyamination of N-tert-Butanesulfinyl lmidates
Ma, PJ (Ma, Peng-Ju); Liu, H (Liu, Hui); Lu, CD (Lu, Chong-Dao); Xu, YJ (Xu, Yan-Jun)
2017
发表期刊ORGANIC LETTERS
ISSN1523-7060
卷号19期号:3页码:670-673
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.

DOI10.1021/acs.orglett.6b03835
收录类别SCI
WOS记录号WOS:000393539900062
引用统计
文献类型期刊论文
条目标识符http://ir.xjipc.cas.cn/handle/365002/5503
专题省部共建新疆特有药用资源利用重点实验室
通讯作者Lu, CD (Lu, Chong-Dao)
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.
条目包含的文件
文件名称/大小 文献类型 版本类型 开放类型 使用许可
Diastereoselective E(351KB)期刊论文作者接受稿开放获取CC BY-NC-SA浏览 请求全文
个性服务
推荐该条目
保存到收藏夹
查看访问统计
导出为Endnote文件
谷歌学术
谷歌学术中相似的文章
[Ma, PJ (Ma, Peng-Ju)]的文章
[Liu, H (Liu, Hui)]的文章
[Lu, CD (Lu, Chong-Dao)]的文章
百度学术
百度学术中相似的文章
[Ma, PJ (Ma, Peng-Ju)]的文章
[Liu, H (Liu, Hui)]的文章
[Lu, CD (Lu, Chong-Dao)]的文章
必应学术
必应学术中相似的文章
[Ma, PJ (Ma, Peng-Ju)]的文章
[Liu, H (Liu, Hui)]的文章
[Lu, CD (Lu, Chong-Dao)]的文章
相关权益政策
暂无数据
收藏/分享
文件名: Diastereoselective Electrophilic α-Hydroxyamination of N-tert-Butanesulfinyl Imidates.pdf
格式: Adobe PDF
所有评论 (0)
暂无评论
 

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。