Rhodium-Catalyzed Enantioselective Addition of Heteroarenium Salts Enabled by Nucleophilic Cyclization of 2-Alkynylanilines

被引:2
作者
Huang, Yaling [1 ]
Qi, Zisong [1 ]
Li, Xingwei [1 ]
机构
[1] Shaanxi Normal Univ SNNU, Sch Chem & Chem Engn, Xian 710062, Shaanxi, Peoples R China
关键词
DEAROMATIZATION; INDOLES; ARYLATION; PYRIDINES; HETEROCYCLES;
D O I
10.1021/acs.orglett.3c03300
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Transition-metal-catalyzed cyclative coupling of 2-alkynylanilines provides a feasible routine for accessing functionalized indoles. Herein, a rhodium-catalyzed highly enantioselective addition of heteroarenium salts is presented, which is enabled by the nucleophilic cyclization of 2-alkynylanilines. It offers feasible protocols to access enantioenriched functionalized indoles tethered to 1,2-dihydropyridine and 1,2-dihydroquinoline motifs with excellent enantioselectivities.
引用
收藏
页码:8439 / 8444
页数:6
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