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Diastereoselective Electrophilic alpha-Hydroxyamination of N-tert-Butanesulfinyl lmidates
Ma, PJ (Ma, Peng-Ju)[ 1,2 ]; Liu, H (Liu, Hui)[ 1 ]; Lu, CD (Lu, Chong-Dao)[ 1 ]; Xu, YJ (Xu, Yan-Jun)[ 1 ]
2017
Source PublicationORGANIC LETTERS
Volume19Issue:3Pages:670-673
Abstract

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
Indexed BySCI
WOS IDWOS:000393539900062
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Document Type期刊论文
Identifierhttp://ir.xjipc.cas.cn/handle/365002/5788
Collection省部共建新疆特有药用资源利用重点实验室
Affiliation1.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
Recommended Citation
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.
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