Enantioselective Synthesis of Chiral Cyclic Hydrazines by Ni-Catalyzed Asymmetric Hydrogenation

被引:12
|
作者
Wang, Siwei [1 ]
Xie, Chaochao [1 ]
Zhu, Yu [1 ]
Zi, Guofu [1 ]
Zhang, Zhanbin [1 ]
Hou, Guohua [1 ,2 ]
机构
[1] Beijing Normal Univ, Coll Chem, Key Lab Radiopharmaceut, Beijing 100875, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai Key Lab Mol Engn Chiral Drugs, Shanghai 200240, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
ALPHA-AMINO-ACID; HYDRAZONES; COMPLEXES; AZAFAGOMINE; LIGANDS; KETONES; IMINES; ESTERS;
D O I
10.1021/acs.orglett.3c01009
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Anefficient Ni-(S,S)-Ph-BPEcomplex that catalyzed asymmetric hydrogenation of cyclic N-acyl hydrazones has been developed to produce variouschiral cyclic hydrazines in high yields with excellent enantioselectivitiesof up to >99% enantiomeric excess. Moreover, the hydrogenationcannot only proceed smoothly on a gram scale under lower catalyst loading(S/C = 3000) without any decrease of enantioselectivity but can alsobe applied to the asymmetric synthesis of a RIP-1 kinase inhibitor.
引用
收藏
页码:3644 / 3648
页数:5
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