Catalytic atroposelective electrophilic amination of diaryl anilines and diaryl phenols for the synthesis of axially chiral diaryl compounds

被引:0
|
作者
Zhu, Haihui [1 ]
Cheng, Long [1 ]
Wang, Jie [1 ]
Han, Zhengyu [1 ]
Sun, Jianwei [2 ]
Huang, Hai [1 ]
机构
[1] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Peoples R China
[2] Hong Kong Univ Sci & Technol, Dept Chem, Kowloon, Clear Water Bay, Hong Kong, Peoples R China
来源
ORGANIC CHEMISTRY FRONTIERS | 2024年 / 11卷 / 23期
基金
中国国家自然科学基金;
关键词
AZODICARBOXYLATE; SULFENYLATION; ATROPISOMERS; RESOLUTION;
D O I
10.1039/d4qo01413h
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Disclosed here is a chiral phosphoric acid-catalyzed atroposelective electrophilic amination reaction, which provides access to a series of axially chiral diaryl compounds through the desymmetric amination reactions of diaryl anilines and diaryl phenols with azodiformates as electrophilic reagents. The reaction could be carried out at room temperature and provide the products with excellent yield and enantioselectivity. A CPA-catalyzed atroposelective electrophilic amination reaction has been developed, which provides access to a series of axially chiral diaryl compounds through the desymmetric amination reactions of diaryl anilines/phenols with azodiformates.
引用
收藏
页码:6672 / 6677
页数:6
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