Asymmetric Transfer Hydrogenation of Trifluoromethylated Imines to Chiral α-Trifluoromethylated Amines With Alcohol as The Hydrogen Source

被引:3
|
作者
Wang, Zheting [1 ]
Yang, Chunhui [1 ]
Chen, Jingchao [1 ]
Yang, Fan [1 ]
Khan, Ruhima [1 ]
Yang, Yong [2 ]
Qiao, Xingfang [2 ]
Su, Zhimin [2 ]
Fan, Baomin [1 ,2 ]
机构
[1] Yunnan Minzu Univ, Key Lab Chem Ethn Med Resources, Yuehua St, Kunming 650500, Yunnan, Peoples R China
[2] Chongqing Acad Chinese Mat Med, Chongqing Key Lab Tradit Chinese Med Hlth, Chongqing, Peoples R China
基金
中国国家自然科学基金;
关键词
Asymmetric transfer hydrogenation; α -Trifluoromethylated imines; Chiral α -trifluoromethylated amines; Alcohols; Deuteration; PARTIALLY-MODIFIED RETRO; CATALYTIC ENANTIOSELECTIVE SYNTHESIS; ACID; REDUCTION; FLUORINE; ARYL; STRATEGIES; INHIBITOR; CHEMISTRY; DISCOVERY;
D O I
10.1002/ajoc.202100201
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An efficient Pd/Zn co-catalyzed method for the asymmetric transfer hydrogenation of trifluoromethylated imines to chiral alpha-trifluoromethylated amines using methanol as the hydrogen source has been developed. The reaction showed good substrate scope and the products were obtained in excellent yields (up to 99%) with excellent enantioselectivity. The present methodology was compatible for the synthesis of deuterated chiral alpha-trifluoromethylated amines. On using CD3OD as the deuterium source, deuterium incorporation up to 98% was observed without compromising the reaction outcome.
引用
收藏
页码:1530 / 1535
页数:6
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